Supelco

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

For this product we use the non-stereospecific CAS number. It is expected that the natural enantiomer is predominant, however the substance is prone to racemization in solution. The product is therefore not specified stereospecifically and is only recommended to be used for non-stereospecific analysis.

grade	analytical standard
Quality Level	100
assay	≥98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	≤5.0% water
Featured Industry	Food and Beverages
format	neat
InChI	1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m1/s1
InChI key	SBHXYTNGIZCORC-CYBMUJFWSA-N

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Erythromycin is a complex macrolide antibiotic drug that exhibits a bacteriostatic activity. It is generally employed in human and veterinary medicines owing to its potential activity against gram positive and a few gram negative strains.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Erythromycin

Empirical Formula (Hill Notation):	C₃₇H₆₇NO₁₃
CAS Number:	114-07-8
Molecular Weight:	733.93
Beilstein/REAXYS Number:	75279
EC Number:	204-040-1
MDL number:	MFCD00084654
PubChem Substance ID:	329823069
NACRES:	NA.24

Erythromycin may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by various chromatography techniques.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Erythromycin is an antibiotic produced by growth of certain strains of Streptomyces erythreus. This product is composed largely of erythromycin A with small amounts of erythromycins B and C and is recommended for concentration at 100 mg/L. Concentrations between 50 and 200 mg/L have also proven effective in controlling bacterial growth. Erythromycin has been used as a motilin receptor agonist, to block respiratory glycoconjugate secretion in human airways in vitro, and for selecting plasmid-cured and recombinant lactococcus lactis MG1363 strains.

Biochem/physiol Actions

Mode of Action: Erythromycin acts by inhibiting elongation at the transpeptidation step, specifically aminoacyl translocation from the A-site to P-site by binding to the 50s subunit of the bacterial 70s rRNA complex.
Antimicrobial Spectrum: This product acts against both gram-negative and gram-positive bacteria.

Caution

This product is stable in solution at 37°C for 3 days. Stock solutions should be stored at 2-8°C.

Preparation Note

This product is soluble in water at 2 mg/mL, with a 0.067% solution in water yielding a pH of 8.0-10.5. It is also soluble in ethanol at 50 mg/mL, yielding a clear, colorless to faint yellow solution. It is freely soluble in alcohol, acetone, chloroform, acetonitrile and ethyl acetate but forms salts with acids. All solutions should be protected from light.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAC3047 in the slot below. This is an example certificate only and may not be the lot that you receive.

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available. This product was designed, produced and verified for accuracy and stability in accordance with ISO/IEC 17025:2005 (AClass Cert AT-1467), ISO GUIDES 34:2009 (AClass Cert AR-1470).

Quality Level	300
grade	certified reference material, pharmaceutical secondary standard
form	neat
CofA	current certificate can be downloaded
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to BP 794, traceable to PhEur E1305000, traceable to USP 1242000
SMILES string	CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
InChI	1S/C37H67NO13/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-/m1/s1
InChI key	ULGZDMOVFRHVEP-RWJQBGPGSA-N

Erythromycin A enol ether (EAEN) is an acidic degradation product of erythromycin A (EA) which is grouped under the macrolide antibiotic class of compounds.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Erythromycin A enol ether

Empirical Formula (Hill Notation):	C₃₇H₆₅NO₁₂
CAS Number:	33396-29-1
Molecular Weight:	715.91
NACRES:	NA.24

EAEN has been used for the analysis of EAEN as degradation product of EA in honey by ultra-performance liquid chromatography equipped with tandem quadrupole mass spectrometer (UPLC-MS/MS) with positive electrospray ionisation (ESI) operating on multiple reaction monitoring (MRM) mode and in rat′s blood plasma, serum and human urine by high performance liquid chromatography-coulometric assay. It may be used as a reference standard for the detection of EAEN in erythromycin fractions by isocratic LC with evaporative light scattering detection (ELSD) and ion trap MS and in commercial erythromycin samples by LC-MS/MS.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	95% (HPLC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H](C3O)N(C)C)[C@@]4(C)CC(C)=C(O4)[C@H](C)[C@@H](O)[C@]1(C)O
InChI	1S/C37H65NO12/c1-14-25-37(10,43)30(40)20(4)28-18(2)16-36(9,50-28)32(49-34-27(39)24(38(11)12)15-19(3)45-34)21(5)29(22(6)33(42)47-25)48-26-17-35(8,44-13)31(41)23(7)46-26/h19-27,29-32,34,39-41,43H,14-17H2,1-13H3/t19-,20+,21+,22-,23+,24+,25-,26+,27-,29+,30-,31+,32-,34+,35-,36-,37-/m1/s1
InChI key	JFVYXJKGJMUGRG-KJPZRSJGSA-N

Erythromycin is an antibiotic produced by growth of certain strains of Streptomyces erythreus. This product is composed largely of erythromycin A with small amounts of erythromycins B and C and is recommended for concentration at 100 mg/L. Concentrations between 50 and 200 mg/L have also proven effective in controlling bacterial growth. Erythromycin has been used as a motilin receptor agonist, to block respiratory glycoconjugate secretion in human airways in vitro, and for selecting plasmid-cured and recombinant lactococcus lactis MG1363 strains.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Erythromycin A hydrate

Empirical Formula (Hill Notation):	C₃₇H₆₇NO₁₃ · xH₂O
CAS Number:	207291-29-0
Molecular Weight:	733.93 (anhydrous basis)
EC Number:	204-040-1
PubChem Substance ID:	329757110
NACRES:	NA.24

Biochem/physiol Actions

Mode of Action: Erythromycin acts by inhibiting elongation at the transpeptidation step, specifically aminoacyl translocation from the A-site to P-site.
Antimicrobial Spectrum: This product acts against both gram-negative and gram-positive bacteria.

Caution

This product is stable in solution at 37°C for 3 days. Stock solutions should be stored at 2-8°C.

Preparation Note

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	200
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
InChI	1S/C37H67NO13.2H2O/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26;;/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3;2*1H2/t18?,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-;;/m1../s1
InChI key	IWGQNYZQLVGGCS-ZKSNWDMWSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Erythrosin B belongs to the class of xanthene dyes, which can find applications as a food colorant.(12} It can exhibit light absorption in the range of 500-550 nm, hence can lead to the formation of reactive oxygen species, which can inactivate the microorganisms, thereby acting like an antimicrobial agent.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Erythrosin B

Empirical Formula (Hill Notation):	C₂₀H₆I₄Na₂O₅
CAS Number:	16423-68-0
Molecular Weight:	879.86
Colour Index Number:	45430
Beilstein/REAXYS Number:	1443945
EC Number:	240-474-8
MDL number:	MFCD00144257
PubChem Substance ID:	329769588
E Number:	E127
NACRES:	NA.24

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	98.0% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	[Na+].[Na+].[O-]c1c(I)cc2c(Oc3c(I)c([O-])c(I)cc3C24OC(=O)c5ccccc45)c1I
InChI	1S/C20H8I4O5.2Na/c21-11-5-9-17(13(23)15(11)25)28-18-10(6-12(22)16(26)14(18)24)20(9)8-4-2-1-3-7(8)19(27)29-20;;/h1-6,25-26H;;/q;2*+1/p-2
InChI key	RAGZEDHHTPQLAI-UHFFFAOYSA-L

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07
signalword	Warning
hcodes	H302 - H413
pcodes	P273 - P301 + P312 + P330
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	359.6 °F - closed cup
Flash Point C	182 °C - closed cup

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Estrone

Empirical Formula (Hill Notation):	C₁₈H₂₂O₂
CAS Number:	53-16-7
Molecular Weight:	270.37
Beilstein/REAXYS Number:	1915077
EC Number:	200-164-5
MDL number:	MFCD00003620
PubChem Substance ID:	329757214

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	200
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	258-260 °C (lit.)
Featured Industry	Pharmaceutical (small molecule)
format	neat
SMILES string	C[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CCC2=O
InChI	1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChI key	DNXHEGUUPJUMQT-CBZIJGRNSA-N
Gene Information	human ... ESR1(2099)

Ethanol, which is derived from cellulosic biomass can find applications as a large-scale transportation fuel. It can serve as a substitute for diesel in compression-ignition engines.

pictograms	GHS08
signalword	Danger
hcodes	H351 - H360FD - H362
pcodes	P202 - P260 - P263 - P264 - P270 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type P2 (EN 143) respirator cartridges
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethanol solution 48075

Empirical Formula (Hill Notation):	C₂H₆O
Linear Formula:	C₂H₅OH
CAS Number:	64-17-5
Molecular Weight:	46.07
Beilstein/REAXYS Number:	1718733
EC Number:	200-659-6
MDL number:	MFCD00003568
PubChem Substance ID:	24871715

General description

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	2000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
SMILES string	CCO
InChI	1S/C2H6O/c1-2-3/h3H,2H2,1H3
InChI key	LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanolamine is a colourless organic compound. It is a strong base and is miscible in water, alcohol, carbon tetrachloride and chloroform. It is highly toxic in nature and is a strong irritant. It is derived from ethylene oxide reacting with ammonia forming mono-, di-, and triethanolamine. It is widely used in manufacturing detergents when reacting with fatty acid. It is most commonly used a corrosion inhibitor.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
Personal Protective Equipment	Eyeshields, Faceshields, Gloves
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 2
Flash Point F	51.8 °F - closed cup
Flash Point C	11 °C - closed cup

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Ethanolamine

Empirical Formula (Hill Notation):	C₂H₇NO
Linear Formula:	NH₂CH₂CH₂OH
CAS Number:	141-43-5
Molecular Weight:	61.08
Beilstein/REAXYS Number:	505944
EC Number:	205-483-3
MDL number:	MFCD00008183
PubChem Substance ID:	329747027
NACRES:	NA.24

Ethanolamine may be used as an analytical standard for the determination of the analyte in cosmetic products, water samples and ethanolamine mixtures by various chromatography techniques.

Quality Level	100
grade	analytical standard
vapor density	2.1 (vs air)
vapor pressure	0.2 mmHg ( 20 °C)
assay	99.5% (GC)
autoignition temp.	1436 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	17 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.454 (lit.), n20/D 1.454
bp	170 °C (lit.), 69-70 °C/10 mmHg
mp	10-11 °C (lit.)
density	1.012 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	NCCO
InChI	1S/C2H7NO/c3-1-2-4/h4H,1-3H2
InChI key	HZAXFHJVJLSVMW-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS05,GHS07
signalword	Danger
hcodes	H302 + H312 + H332 - H314 - H335 - H412
pcodes	P273 - P280 - P301 + P312 + P330 - P303 + P361 + P353 - P304 + P340 + P312 - P305 + P351 + P338 + P310
Target Organs	Respiratory system
Personal Protective Equipment	Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
RIDADR	UN 2491 8 / PGIII
WGK Germany	WGK 1
Flash Point F	195.8 °F - Pensky-Martens closed cup
Flash Point C	91 °C - Pensky-Martens closed cup

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Ethosuximide

Empirical Formula (Hill Notation):	C₇H₁₁NO₂
CAS Number:	77-67-8
Molecular Weight:	141.17
EC Number:	201-048-7
MDL number:	MFCD00072123
PubChem Substance ID:	329760914
NACRES:	NA.24

Quality Level	100
grade	analytical standard
assay	98.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	O=C1NC(CC1(C)CC)=O
InChI	1S/C7H11NO2/c1-3-7(2)4-5(9)8-6(7)10/h3-4H2,1-2H3,(H,8,9,10)
InChI key	HAPOVYFOVVWLRS-UHFFFAOYSA-N
Gene Information	human ... CACNA1G(8913), CACNA1H(8912), CACNA1I(8911)

Ethyl acetate can be obtained via esterification reaction between ethyl alcohol and acetic acid in the presence of sulfuric acid. It can find applications as a solvent in the production of inks, varnishes, fat, nitrocellulose, etc. It can also be used as a cleaning agent in textile industry and as a flavoring agent for in food and pharmaceutical industries. It can also serve as a substitute for methyl ethyl ketone in food industry.

pictograms	GHS07
signalword	Warning
hcodes	H302
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethyl acetate solution 47947

CAS Number:	141-78-6
EC Number:	200-659-6

General description

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	2000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
InChI	1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
InChI key	XEKOWRVHYACXOJ-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethyl acrylate can undergo anionic polymerization upon initiation by tetrabutylammonium azide in the presence of alkylaluminum bisphenoxides in toluene to yield azide-end poly(ethyl acrylate) (PEA).

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P311
Target Organs	Eyes
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 1
Flash Point F	51.8 °F - closed cup
Flash Point C	11 °C - closed cup

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Ethyl acrylate

Empirical Formula (Hill Notation):	C₅H₈O₂
Linear Formula:	CH₂=CHCOOC₂H₅
CAS Number:	140-88-5
Molecular Weight:	100.12
Beilstein/REAXYS Number:	773866
EC Number:	205-438-8
MDL number:	MFCD00009188
PubChem Substance ID:	329766922
NACRES:	NA.24

Quality Level	100
grade	analytical standard
vapor density	3.5 (vs air)
vapor pressure	31 mmHg ( 20 °C)
assay	99.5% (GC)
form	neat
autoignition temp.	721 °F
shelf life	limited shelf life, expiry date on the label
contains	~0.002% hydroquinone monomethyl ether as stabilizer
expl. lim.	12.1 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.406 (lit.), n20/D 1.406
bp	99 °C (lit.)
mp	71 °C (lit.)
density	0.921 g/mL at 20 °C, 0.918 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care Petroleum
format	neat
SMILES string	CCOC(=O)C=C
InChI	1S/C5H8O2/c1-3-5(6)7-4-2/h3H,1,4H2,2H3
InChI key	JIGUQPWFLRLWPJ-UHFFFAOYSA-N

Ethyl butyrate belongs to the class of esters and is generally employed as a flavor enhancer in commercial food products.

pictograms	GHS02,GHS06
signalword	Danger
hcodes	H225 - H302 + H312 - H315 - H317 - H319 - H331 - H335 - H412
pcodes	P210 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P311
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 1917 3 / PGII
WGK Germany	WGK 2
Flash Point F	48.2 °F - closed cup
Flash Point C	9 °C - closed cup

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Ethyl butyrate

Empirical Formula (Hill Notation):	C₆H₁₂O₂
Linear Formula:	CH₃CH₂CH₂C(O)OC₂H₅
CAS Number:	105-54-4
Molecular Weight:	116.16
Beilstein/REAXYS Number:	506331
EC Number:	203-306-4
MDL number:	MFCD00009394
PubChem Substance ID:	329766522
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethyl butyrate may be used as an analytical reference standard for the quantification of the analyte in orange essence oil samples and has been used as a reference standard for the determination of the analyte in dry and sweet white wines using different chromatography techniques.

Quality Level	200
grade	analytical standard
vapor density	4 (vs air)
vapor pressure	15.5 mmHg ( 25 °C)
assay	99.5% (GC)
form	neat
autoignition temp.	865 °F
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.392 (lit.), n20/D 1.393
bp	120 °C (lit.)
mp	93 °C (lit.)
density	0.875 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CCCC(=O)OCC
InChI	1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3
InChI key	OBNCKNCVKJNDBV-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethyl cinnamate may be used as a reference standard:

pictograms	GHS02
signalword	Warning
hcodes	H226
pcodes	P210
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1180 - class 3 - PG 3 - Ethyl butyrate
WGK Germany	WGK 1
Flash Point F	78.8 °F
Flash Point C	26 °C

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Ethyl cinnamate

Empirical Formula (Hill Notation):	C₁₁H₁₂O₂
Linear Formula:	C₆H₅CH=CHCOOC₂H₅
CAS Number:	103-36-6
Molecular Weight:	176.21
Beilstein/REAXYS Number:	775541
EC Number:	203-104-6
MDL number:	MFCD00009189
PubChem Substance ID:	329760317
NACRES:	NA.24

to determine the toxic effects of ethyl cinnamate, affecting the growth, photosynthesis and cell physiology of Chlorella vulgaris, a dominant species of green algae based on chlorophyll fluorescence and flow cytometry analysis.
in the determination of ethyl cinnamate in samples of red wine using gas chromatography coupled with ion-trap mass spectrometric analysis technique (GC-MS).

Quality Level	100
grade	analytical standard
assay	98.5% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	0.3% water
refractive index	n20/D 1.558 (lit.), n20/D 1.559-1.561
bp	271 °C (lit.)
mp	6-8 °C (lit.)
density	1.049 g/mL at 20 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
storage temp.	2-8°C
SMILES string	CCOC(=O)\C=C\c1ccccc1
InChI	1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+
InChI key	KBEBGUQPQBELIU-CMDGGOBGSA-N

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethyl ethanesulfonate

Empirical Formula (Hill Notation):	C₄H₁₀O₃S
CAS Number:	1912-30-7
Molecular Weight:	138.19
Beilstein/REAXYS Number:	1748749
MDL number:	MFCD01728649
PubChem Substance ID:	329753607
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental Pharmaceutical
format	neat
storage temp.	2-8°C
SMILES string	CCOS(=O)(=O)CC
InChI	1S/C4H10O3S/c1-3-7-8(5,6)4-2/h3-4H2,1-2H3
InChI key	PPCXFTKZPBHXIW-UHFFFAOYSA-N

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethyl ether solution 47948

CAS Number:	60-29-7
EC Number:	200-659-6

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	2000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
InChI	1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3
InChI key	RTZKZFJDLAIYFH-UHFFFAOYSA-N

Ethyl formate belongs to the group of ethyl esters, which can be synthesized via the reaction between formic acid and ethanol in the presence of sulfuric acid, under thermal conditions.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 2
Flash Point F	49.5 °F
Flash Point C	9.7 °C

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Ethyl formate

Empirical Formula (Hill Notation):	C₃H₆O₂
Linear Formula:	HCOOC₂H₅
CAS Number:	109-94-4
Molecular Weight:	74.08
Beilstein/REAXYS Number:	906769
EC Number:	203-721-0
MDL number:	MFCD00003294
eCl@ss:	39022251
PubChem Substance ID:	329769660
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethyl formate may be used as an analytical standard for the determination of the analyte in fruits, bread pre-ferment brew, alcoholic beverages, smog and gasoline samples by gas chromatography (GC) based techniques.

Quality Level	100
grade	analytical standard
vapor density	2.5 (vs air)
vapor pressure	15.16 psi ( 55 °C), 3.79 psi ( 20 °C)
assay	99.5% (GC)
form	neat
autoignition temp.	851 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	16 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.359 (lit.), n20/D 1.360
bp	52-54 °C (lit.)
mp	80 °C (lit.)
density	0.921 g/mL at 20 °C (lit.)
Featured Industry	Agriculture Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CCOC=O
InChI	1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3
InChI key	WBJINCZRORDGAQ-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H302 + H332 - H319 - H335
pcodes	P210 - P233 - P240 - P301 + P312 - P304 + P340 + P312 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves
RIDADR	UN1190 - class 3 - PG 2 - Ethyl formate
WGK Germany	WGK 1
Flash Point F	-4.0 °F - closed cup
Flash Point C	-20 °C - closed cup

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Ethyl methanesulfonate

Empirical Formula (Hill Notation):	C₃H₈O₃S
Linear Formula:	CH₃SO₃CH₂CH₃
CAS Number:	62-50-0
Molecular Weight:	124.16
Beilstein/REAXYS Number:	773969
EC Number:	200-536-7
MDL number:	MFCD00007559
PubChem Substance ID:	329764478
NACRES:	NA.24

Bottomless glass bottle. Contents are inside inserted fused cone.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.418 (lit.)
bp	85-86 °C/10 mmHg (lit.)
density	1.206 g/mL at 20 °C
Featured Industry	Environmental Pharmaceutical
format	neat
storage temp.	2-8°C
SMILES string	CCOS(C)(=O)=O
InChI	1S/C3H8O3S/c1-3-6-7(2,4)5/h3H2,1-2H3
InChI key	PLUBXMRUUVWRLT-UHFFFAOYSA-N

Ethyl propionate is an ethyl ester of propionic acid and is commonly used as a flavoring agent in food products.

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H340 - H350 - H361f
pcodes	P201 - P301 + P312 + P330 - P308 + P313
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	212.0 °F
Flash Point C	100 °C

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Ethyl propionate

Empirical Formula (Hill Notation):	C₅H₁₀O₂
Linear Formula:	CH₃CH₂COOC₂H₅
CAS Number:	105-37-3
Molecular Weight:	102.13
Beilstein/REAXYS Number:	506287
EC Number:	203-291-4
MDL number:	MFCD00009308
PubChem Substance ID:	329770529
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethyl propionate may be used as an analytical reference standard for the quantification of the analyte in aqueous essence and fruit juice samples using different chromatography techniques.

Quality Level	200
grade	analytical standard
vapor density	3.52 (vs air)
vapor pressure	40 mmHg ( 27.2 °C)
assay	99.7% (GC)
form	neat
autoignition temp.	887 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	11 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.384 (lit.), n20/D 1.384
bp	99 °C (lit.)
mp	73 °C (lit.)
density	0.888 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CCOC(=O)CC
InChI	1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3
InChI key	FKRCODPIKNYEAC-UHFFFAOYSA-N

Purity (GC): 99.5
Identity (IR-spectrum): conforms

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H315 - H319 - H335
pcodes	P210 - P233 - P240 - P241 - P303 + P361 + P353 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1195 - class 3 - PG 2 - Ethyl propionate
WGK Germany	WGK 1
Flash Point F	53.6 °F - closed cup
Flash Point C	12 °C - closed cup

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Ethylbenzene

Empirical Formula (Hill Notation):	C₈H₁₀
CAS Number:	100-41-4
Molecular Weight:	106.17
MDL number:	MFCD00011647
EC Index Number:	202-849-4

storage conditions	Store at +5°C to +30°C.
Quality Level	100
vapor pressure	9.5 hPa ( 20 °C)
assay	99.5% (GC)
form	liquid
autoignition temp.	430 °C
potency	3500 mg/kg LD₅₀, oral (Rat), 15354 mg/kg LD₅₀, skin (Rabbit)
expl. lim.	1.0-7.8 % (v/v)
application(s)	gas chromatography (GC): suitable
kinematic viscosity	0.63 cSt(40 °C)
bp	136 °C/1013 hPa
mp	-95 °C
transition temp	flash point 15 °C
solubility	0.2 g/L
density	0.87 g/cm³ at 20 °C
storage temp.	2-30°C
InChI	1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI key	YNQLUTRBYVCPMQ-UHFFFAOYSA-N

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Ethylbenzene solution 40036

Empirical Formula (Hill Notation):	C₈H₁₀
CAS Number:	100-41-4
Molecular Weight:	106.17
MDL number:	MFCD00011647
PubChem Substance ID:	24864910

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	5000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
SMILES string	CCc1ccccc1
InChI	1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI key	YNQLUTRBYVCPMQ-UHFFFAOYSA-N

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 2
Flash Point F	51.8 °F - closed cup
Flash Point C	11 °C - closed cup

25,82 € / 2 427 ₽

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Ethylbenzene-d10 solution 48942

CAS Number:	25837-05-2
EC Number:	200-659-6

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	2000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
InChI	1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3/i1D3,2D2,3D,4D,5D,6D,7D
InChI key	YNQLUTRBYVCPMQ-CFTAVCBPSA-N

Ethylene glycol is a colorless liquid, which may be obtained via hydration of ethylene oxide.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
RIDADR	UN1230 - class 3 - PG 2 - Methanol
WGK Germany	WGK 2
Flash Point F	49.5 °F - Solvent
Flash Point C	9.7 °C - Solvent

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Ethylene glycol

Empirical Formula (Hill Notation):	C₂H₆O₂
Linear Formula:	HOCH₂CH₂OH
CAS Number:	107-21-1
Molecular Weight:	62.07
Beilstein/REAXYS Number:	505945
EC Number:	203-473-3
MDL number:	MFCD00002885
eCl@ss:	39020501
PubChem Substance ID:	329769431
NACRES:	NA.24

It may be used as an analytical standard for the determination of the analyte in biological samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethylene glycol has been used as a solvent in the synthesis of silver nanostructures, which serve as effective catalysts in the epoxidation reaction of ethylene.

Quality Level	100
grade	analytical standard
vapor density	2.1 (vs air)
vapor pressure	0.08 mmHg ( 20 °C)
assay	99.9% (GC)
form	neat
autoignition temp.	752 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	15.3 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.431 (lit.), n20/D 1.431
bp	195-198 °C
mp	13 °C (lit.)
density	1.113 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	OCCO
InChI	1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2
InChI key	LYCAIKOWRPUZTN-UHFFFAOYSA-N

Ethylene glycol butyl ether can find applications as a surfactant in investigating the process of spreading, shrinking and resting regime on the surface of water. It can also find applications as a cosolvent in water-borne paints.

pictograms	GHS07,GHS08
signalword	Warning
hcodes	H302 - H373
pcodes	P260 - P301 + P312 + P330
Target Organs	Kidney
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 1

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Ethylene glycol butyl ether

Empirical Formula (Hill Notation):	C₆H₁₄O₂
Linear Formula:	CH₃(CH₂)₃OCH₂CH₂OH
CAS Number:	111-76-2
Molecular Weight:	118.17
Beilstein/REAXYS Number:	1732511
EC Number:	203-905-0
MDL number:	MFCD00002884
PubChem Substance ID:	329757913
NACRES:	NA.24

Ethylene glycol butyl ether may be used as an analytical standard for the determination of the analyte in biological samples, environmental samples, cleaning products, detergents, and organic solvent mixtures by gas chromatography (GC) based techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
vapor density	4.1 (vs air)
vapor pressure	<1 mmHg ( 20 °C), 10 mmHg ( 81 °C)
assay	99.5% (GC)
form	neat
autoignition temp.	473 °F
shelf life	limited shelf life, expiry date on the label
composition	Water, 0.1% (coulometer)
expl. lim.	10.6 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.419 (lit.), n20/D 1.420
bp	169-172.5 °C (lit.)
mp	75 °C (lit.)
density	0.902 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CCCCOCCO
InChI	1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3
InChI key	POAOYUHQDCAZBD-UHFFFAOYSA-N

The purity is calculated based on the principle of mass balance and is mentioned on the CoA

pictograms	GHS07
signalword	Warning
hcodes	H302 + H332 - H315 - H319
pcodes	P261 - P264 - P301 + P312 - P302 + P352 - P304 + P340 + P312 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	NA 1993 / PGIII
WGK Germany	WGK 1
Flash Point F	152.6 °F - Pensky-Martens closed cup
Flash Point C	67 °C - Pensky-Martens closed cup

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Ethylene glycol diacrylate

Empirical Formula (Hill Notation):	C₈H₁₀O₄
Linear Formula:	(H₂C=CHCO₂CH₂-)₂
CAS Number:	2274-11-5
Molecular Weight:	170.16
EC Number:	218-886-4
MDL number:	MFCD00008629
PubChem Substance ID:	329756124
NACRES:	NA.24

Quality Level	100
grade	analytical standard
assay	98.0% (GC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.453 (lit.)
bp	66-68 °C/2 mmHg (lit.)
density	1.094 g/mL at 25 °C (lit.)
Featured Industry	Environmental Pharmaceutical
format	neat
SMILES string	C=CC(=O)OCCOC(=O)C=C
InChI	1S/C8H10O4/c1-3-7(9)11-5-6-12-8(10)4-2/h3-4H,1-2,5-6H2
InChI key	KUDUQBURMYMBIJ-UHFFFAOYSA-N

Общее описание
Система проверки квалификации фармацевтических работников разработана с учетом потребностей фармацевтической промышленности.
Образцы pharma PT позволяют лабораториям продемонстрировать свою компетентность в применении стандартных методов анализа USP. Они могут быть использованы для подтверждения аккредитаторами или аудиторами того, что лабораторные процессы выполняются надлежащим образом. Наша фармацевтическая схема PT охватывает такие категории продуктов, как химические тесты и анализатор, физические тесты и определения, а также микробиологические тесты.
Тип схемы PT: Фармацевтическая
Матрица: Метанол
Анализируемые вещества: Значения анализируемых веществ варьируются от партии к партии.
Всю информацию об использовании тяжелых металлов в стандартах проверки качества сырья для фармацевтических препаратов можно найти в пакете отчетов, который можно загрузить по адресу
Приложение
Оксид этилена подходит для определения концентрации анализируемого вещества оксида этилена в метаноле.
График проведения квалификационных испытаний (2021-2022)
Аптечный
ФАРМ21-4, 6 октября - 19 ноября 2021 г.
Для данного продукта не доступно экспресс-исследование
Особенности и преимущества
У нас есть обширное портфолио экологических программ PT с образцами, "подходящими по назначению", которые помогут вам удовлетворить потребности лаборатории.
Наша программа тестирования квалификации (PT) является эталоном для:
    предоставьте сотрудникам представление о работе их лабораторий, чтобы убедиться в точности и надежности процесса тестирования
    сравните результаты с результатами других лабораторий на национальном и международном уровнях
    проведите тестирование и обучение персонала, чтобы лучше понять влияние неправильных результатов и выявить области, в которых могут возникнуть проблемы.
    провести независимую оценку работы лаборатории
    продемонстрировать клиентам, коллегам и органам по аккредитации свою приверженность качеству

Примечание к подготовке
Описание
    Объем пробы составляет 1,2 мл.
    Проба предназначена для ГХ- и ГХ/МС-анализа.

Подготовка пробы
    Перед использованием образец не нуждается в специальной обработке
    Используйте стандартную процедуру подготовки образца

Анализ
    Для анализа образца используйте свой стандартный метод анализа
    Сообщите о результатах в виде мкг/мл на портале профессионального тестирования

Хранение и стабильность
Пожалуйста, ознакомьтесь с этикеткой образца, чтобы узнать срок годности, конкретную температуру и условия хранения.
Другие примечания
Нажмите здесь, чтобы узнать больше об ускоренных курсах обучения (тестах на квалификацию по запросу, которые предлагаются в зависимости от наличия партии). Результаты экспресс-тестирования публикуются в течение 48-72 часов, в то время как отчеты о запланированных исследованиях публикуются в течение 21 дня.

pictograms	GHS06,GHS09
signalword	Danger
hcodes	H301 - H312 + H332 - H315 - H319 - H335 - H411
pcodes	P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	UN2810 - class 6.1 - PG 3 - EHS - Toxic, liquids, organic, n.o.s., HI: all
WGK Germany	WGK 3
Flash Point F	213.8 °F - closed cup
Flash Point C	101 °C - closed cup

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Окись этилена PE1206-1.2ML Supelco

Информация по технике безопасности

Упаковка	pkg of 1.2 mL
Избранная отрасль	Фармацевтика
Температура хранения	2-8°C

Пиктограммы	GHS02,GHS04,GHS05,GHS06,GHS08
Сигнальное слово	Danger
Указания на опасность	H220 - H230 - H280 - H301 + H331 - H314 - H335 - H336 - H340 - H350 - H360FD - H372
Меры предосторожности	P202 - P210 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P403 + P233 - P410 + P403
Целевые органы	Нервная система
WGK Germany	WGK 3
Flash Point(F)	-4.0 °F - закрытая чашка
Flash Point(C)	-20.0 °C - закрытая чашка

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Ethylene oxide solution 48838

Empirical Formula (Hill Notation):	C₂H₄O
CAS Number:	75-21-8
Molecular Weight:	44.05
MDL number:	MFCD00014482
PubChem Substance ID:	329757418

General description

Ethylene oxide is a toxic and flammable liquid, which can be obtained via vapor phase oxidation of ethylene. It can be used in the synthesis of ethylene glycol, glycol ethers, surfactants and ethanolamines. It is an industrially important chemical, that can be used as fumigant to sterilize dental and medical equipments.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
feature	standard type calibration
packaging	ampule of 1 mL
concentration	50 mg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Agriculture Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution
storage temp.	2-8°C
SMILES string	C1CO1
InChI	1S/C2H4O/c1-2-3-1/h1-2H2
InChI key	IAYPIBMASNFSPL-UHFFFAOYSA-N

Pictograms	GHS02,GHS05,GHS06,GHS08
Signal Word	Danger
Hazard Statements	H225 - H301 + H311 + H331 - H314 - H340 - H350 - H360FD - H370 - H373
Precautionary Statements	P201 - P210 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Target Organs	Eyes, Nervous system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 3
Flash Point(F)	50.0 °F - closed cup
Flash Point(C)	10 °C - closed cup

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Ethylene oxide solution CRM47949

Empirical Formula (Hill Notation):	C₂H₄O
CAS Number:	75-21-8
Molecular Weight:	44.05
MDL number:	MFCD00014482
PubChem Substance ID:	329798452
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	2000 µg/mL in dichloromethane
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Agriculture Cleaning Products Cosmetics Food and Beverages Personal Care
format	single component solution
storage temp.	2-8°C
SMILES string	C1CO1
InChI	1S/C2H4O/c1-2-3-1/h1-2H2
InChI key	IAYPIBMASNFSPL-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H315 - H319 - H336 - H340 - H350
pcodes	P202 - P261 - P264 - P302 + P352 - P305 + P351 + P338 - P308 + P313
Target Organs	Central nervous system
RIDADR	UN 1593 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethylenediamine

Empirical Formula (Hill Notation):	C₂H₈N₂
Linear Formula:	NH₂CH₂CH₂NH₂
CAS Number:	107-15-3
Molecular Weight:	60.10
Beilstein/REAXYS Number:	605263
EC Number:	203-468-6
MDL number:	MFCD00008204
eCl@ss:	39030201
PubChem Substance ID:	329756044
NACRES:	NA.24

Quality Level	100
grade	analytical standard
vapor density	2.07 (vs air)
vapor pressure	10 mmHg ( 20 °C)
assay	99.8% (GC)
form	neat
autoignition temp.	716 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	16 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.456, n20/D 1.4565 (lit.)
bp	118 °C (lit.)
mp	8.5 °C (lit.)
solubility	H₂O: soluble at
density	0.899 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	NCCN
InChI	1S/C2H8N2/c3-1-2-4/h1-4H2
InChI key	PIICEJLVQHRZGT-UHFFFAOYSA-N

Ethylhexyl triazone is a ultraviolet-B filter, which is used as a sunscreen agent in skin care products.
Ethylhexyl triazone has a high absorption coefficient and photostability, which makes it an important ingredient in cosmetic formulations, where high SPF value is required.

pictograms	GHS02,GHS05,GHS06,GHS08
signalword	Danger
hcodes	H226 - H302 + H332 - H311 - H314 - H317 - H334 - H412
pcodes	P210 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Personal Protective Equipment	Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
RIDADR	UN 1604 3(8) / PGII
WGK Germany	WGK 1
Flash Point F	100.4 °F - closed cup
Flash Point C	38 °C - closed cup

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Ethylhexyl triazone

Empirical Formula (Hill Notation):	C₄₈H₆₆N₆O₆
CAS Number:	88122-99-0
Molecular Weight:	823.07
Beilstein/REAXYS Number:	11001015
EC Number:	402-070-1
MDL number:	MFCD09753106
PubChem Substance ID:	329770240
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Ethylhexyl triazone may be used as an analytical reference standard for the quantification of the analyte in the following:

Cosmetic samples using ultra-high-performance supercritical fluid chromatography (UHPSFC).
Topical skincare products using normal-phase high-performance thin layer chromatography (HPTLC) and densitometry.
Environmental samples using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	5% water (calc. from elemental analysis)
mp	128-132 °C
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	CCCCC(CC)COC(=O)c1ccc(Nc2nc(Nc3ccc(cc3)C(=O)OCC(CC)CCCC)nc(Nc4ccc(cc4)C(=O)OCC(CC)CCCC)n2)cc1
InChI	1S/C48H66N6O6/c1-7-13-16-34(10-4)31-58-43(55)37-19-25-40(26-20-37)49-46-52-47(50-41-27-21-38(22-28-41)44(56)59-32-35(11-5)17-14-8-2)54-48(53-46)51-42-29-23-39(24-30-42)45(57)60-33-36(12-6)18-15-9-3/h19-30,34-36H,7-18,31-33H2,1-6H3,(H3,49,50,51,52,53,54)
InChI key	JGUMTYWKIBJSTN-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

hcodes	H413
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	584.6 °F
Flash Point C	307 °C

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Ethylhydrocupreine

Empirical Formula (Hill Notation):	C₂₁H₂₈N₂O₂
CAS Number:	522-60-1
Molecular Weight:	340.46
EC Number:	208-333-5
MDL number:	MFCD00135595
PubChem Substance ID:	329799076
NACRES:	NA.24

grade	analytical standard
Quality Level	100
assay	95%
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
storage temp.	2-8°C
SMILES string	CCOc1ccc2nccc([C@@H](O)[C@@H]3C[C@@H]4CCN3C[C@@H]4CC)c2c1
InChI	1S/C21H28N2O2/c1-3-14-13-23-10-8-15(14)11-20(23)21(24)17-7-9-22-19-6-5-16(25-4-2)12-18(17)19/h5-7,9,12,14-15,20-21,24H,3-4,8,10-11,13H2,1-2H3/t14-,15-,20-,21+/m0/s1
InChI key	SUWZHLCNFQWNPE-LATRNWQMSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sensitive and specific reagent for the identification of Streptococcus pneumoniae.

pictograms	GHS07
signalword	Warning
hcodes	H302
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Ethylhydrocupreine hydrochloride

Empirical Formula (Hill Notation):	C₂₁H₂₈N₂O₂ · HCl
CAS Number:	3413-58-9
Molecular Weight:	376.92
Beilstein/REAXYS Number:	4055970
EC Number:	222-302-3
MDL number:	MFCD00135594
PubChem Substance ID:	329799090
NACRES:	NA.24

grade	analytical standard
Quality Level	100
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
storage temp.	2-8°C
SMILES string	Cl[H].[H][C@@]12CCN(C[C@@H]1CC)[C@@]([H])(C2)[C@H](O)c3ccnc4ccc(OCC)cc34
InChI	1S/C21H28N2O2.ClH/c1-3-14-13-23-10-8-15(14)11-20(23)21(24)17-7-9-22-19-6-5-16(25-4-2)12-18(17)19;/h5-7,9,12,14-15,20-21,24H,3-4,8,10-11,13H2,1-2H3;1H/t14-,15-,20-,21+;/m0./s1
InChI key	QNRATNLHPGXHMA-XZHTYLCXSA-N

Etoricoxib is a non-steroidal cyclooxygenase-2 (COX-2) selective anti-inflammatory drug mostly used to treat patients suffering from osteoarthritis and rheumatoid arthritis.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Etoricoxib

Empirical Formula (Hill Notation):	C₁₈H₁₅ClN₂O₂S
CAS Number:	202409-33-4
Molecular Weight:	358.84
Beilstein/REAXYS Number:	8073797
MDL number:	MFCD06797512
PubChem Substance ID:	329753738
NACRES:	NA.24

Etoricoxib may have been used as reference standard in liquid chromatography-tandem mass spectrometry method with atmospheric pressure chemical ionization (LC-APCI/MS/MS) method for determination of etoricoxib from human plasma.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
storage temp.	2-8°C
SMILES string	Cc1ccc(cn1)-c2ncc(Cl)cc2-c3ccc(cc3)S(C)(=O)=O
InChI	1S/C18H15ClN2O2S/c1-12-3-4-14(10-20-12)18-17(9-15(19)11-21-18)13-5-7-16(8-6-13)24(2,22)23/h3-11H,1-2H3
InChI key	MNJVRJDLRVPLFE-UHFFFAOYSA-N
Gene Information	human ... PTGS2(5743)

Famprofazone is a pyrazole derivative and belongs to the class of non-steroidal anti-inflammatory drugs. It is widely used as an analgesic and antipyretic in medical applications.

pictograms	GHS06
signalword	Danger
hcodes	H302 - H310
pcodes	P262 - P264 - P270 - P280 - P301 + P312 - P302 + P352 + P310
RIDADR	UN 2811 6.1 / PGII
WGK Germany	WGK 3

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Famprofazone

Empirical Formula (Hill Notation):	C₂₄H₃₁N₃O
CAS Number:	22881-35-2
Molecular Weight:	377.52
EC Number:	245-284-9
MDL number:	MFCD00079304
PubChem Substance ID:	329799771
NACRES:	NA.24

Famprofazone may be used as an analytical reference standard for the quantification of the analyte in biological samples using liquid chromatography coupled to tandem mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

10 g in poly bottle

grade	analytical standard
Quality Level	200
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	CC(C)C1=C(CN(C)C(C)Cc2ccccc2)N(C)N(c3ccccc3)C1=O
InChI	1S/C24H31N3O/c1-18(2)23-22(17-25(4)19(3)16-20-12-8-6-9-13-20)26(5)27(24(23)28)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3
InChI key	GNUXVOXXWGNPIV-UHFFFAOYSA-N

Fast Green FCF is a synthetic organic dye, which belongs to the triphenylmethane group. It can be found in a wide range of applications in food and beverage industry. It can also be used in scientific research for the staining of proteins and identification of extracellular recording or injection sites in electrophysiological experiments.

pictograms	GHS07
signalword	Warning
hcodes	H302
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fast Green FCF

Empirical Formula (Hill Notation):	C₃₇H₃₄N₂Na₂O₁₀S₃
Linear Formula:	C₃₇H₃₄N₂O₁₀S₃Na₂
CAS Number:	2353-45-9
Molecular Weight:	808.85
Colour Index Number:	42053
Beilstein/REAXYS Number:	5718212
EC Number:	219-091-5
MDL number:	MFCD00013053
PubChem Substance ID:	329761116
E Number:	E143
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fast Green FCF dye is used for protein staining in IEF, native PAGE and SDS-PAGE. Fast Green staining is linear over a wider range of protein concentrations than Brilliant Blue R. After electrophoresis, fixing the proteins in the gel is recommended for maximum sensitivity. The gel can then be stained for 2 hr with 0.1% Fast Green FCF in either 30% (v/v) ethanol, 10% (v/v) acetic acid or in 7% acetic acid. The gel can be destained with either 30% (v/v) ethanol, 10% (v/v) acetic acid, or 7% acetic acid. The stained gel can be scanned at 625 nm. The detection sensitivity is approx. 30% that with Brilliant Blue R.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	98.0% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	290 °C (dec.) (lit.)
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	[Na+].[Na+].CCN(Cc1cccc(c1)S([O-])(=O)=O)c2ccc(cc2)C(=C3/C=CC(\C=C3)=[N+](\CC)Cc4cccc(c4)S([O-])(=O)=O)\c5ccc(O)cc5S([O-])(=O)=O
InChI	1S/C37H36N2O10S3.2Na/c1-3-38(24-26-7-5-9-33(21-26)50(41,42)43)30-15-11-28(12-16-30)37(35-20-19-32(40)23-36(35)52(47,48)49)29-13-17-31(18-14-29)39(4-2)25-27-8-6-10-34(22-27)51(44,45)46;;/h5-23H,3-4,24-25H2,1-2H3,(H3,41,42,43,44,45,46,47,48,49);;/q;2*+1/p-2
InChI key	RZSYLLSAWYUBPE-UHFFFAOYSA-L

Fast Yellow AB (E-105) is used for the quality control in food products. It belongs to the class of water-soluble food color additives. These synthetic food colors are commonly used for the maintenance and improvement of color appearance in foods. Fast Yellow AB is one of the most recalcitrant of the azo dyes due to the arrangement of withdrawing substituents.

pictograms	GHS08
signalword	Warning
hcodes	H341
pcodes	P281
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Fast Yellow AB

Linear Formula:	C₁₂H₁₁N₃O₆S₂xNA
CAS Number:	79873-36-2
E Number:	E105
NACRES:	NA.24

Fast Yellow AB may be used as an analytical reference standard for the quantification of the analyte in:

Drinks and candies using reversed-phase high-performance liquid chromatography with photodiode array detection.
Commercial products such as sports drinks and bakery ink formulations using high-performance thin layer chromatography.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	97.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat

Fenbendazole is a thio substituted benzimidazole, which belongs to the group of anthelmintics. It can be widely used in veterinary medicine particularly, in the treatment of helminth infections.
Chemical structure: benzimidazole

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Fenbendazole

Empirical Formula (Hill Notation):	C₁₅H₁₃N₃O₂S
CAS Number:	43210-67-9
Molecular Weight:	299.35
Beilstein/REAXYS Number:	759077
EC Number:	256-145-7
MDL number:	MFCD00144301
PubChem Substance ID:	329755115
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	COC(=O)Nc1nc2cc(Sc3ccccc3)ccc2[nH]1
InChI	1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChI key	HDDSHPAODJUKPD-UHFFFAOYSA-N

Chemical structure: benzimidazole

pictograms	GHS08,GHS09
signalword	Warning
hcodes	H361fd - H373 - H410
pcodes	P201 - P202 - P260 - P273 - P280 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fenbendazole sulfone

Empirical Formula (Hill Notation):	C₁₅H₁₃N₃O₄S
CAS Number:	54029-20-8
Molecular Weight:	331.35
Beilstein/REAXYS Number:	703211
MDL number:	MFCD00797921
PubChem Substance ID:	329754020
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	COC(=O)Nc1nc2cc(ccc2[nH]1)S(=O)(=O)c3ccccc3
InChI	1S/C15H13N3O4S/c1-22-15(19)18-14-16-12-8-7-11(9-13(12)17-14)23(20,21)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChI key	UAFDGCOOJPIAHN-UHFFFAOYSA-N

Chemical structure: benzimidazole

pictograms	GHS07,GHS09,GHS07,GHS09
signalword	Warning-Warning
hcodes	H302 - H315 - H317 - H410 - H302 - H315 - H317 - H410
pcodes	P261 - P264 - P273 - P280 - P261 - P264 - P273 - P280 - P301 + P312 - P302 + P352 - P301 + P312 - P302 + P352
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fenbendazole-d3

Empirical Formula (Hill Notation):	C₁₅D₃H₁₀N₃O₂S
CAS Number:	1228182-47-5
Molecular Weight:	302.37
MDL number:	MFCD16652570
PubChem Substance ID:	329754031
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
mass shift	M+3
SMILES string	[2H]C([2H])([2H])OC(=O)Nc1nc2cc(Sc3ccccc3)ccc2[nH]1
InChI	1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)/i1D3
InChI key	HDDSHPAODJUKPD-FIBGUPNXSA-N

Fenbufen belongs to the class of non-steroidal anti-inflammatory drugs, widely used as an antipyretic and analgesic in medical applications. Its mode of action involves the inhibition of cyclooxygenase enzyme and thereby prevents the synthesis of certain prostaglandins.

pictograms	GHS08,GHS09
signalword	Warning
hcodes	H361fd - H373 - H410
pcodes	P201 - P202 - P260 - P273 - P280 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fenbufen

Empirical Formula (Hill Notation):	C₁₆H₁₄O₃
Linear Formula:	C₆H₅C₆H₄CO(CH₂)₂CO₂H
CAS Number:	36330-85-5
Molecular Weight:	254.28
EC Number:	252-979-0
MDL number:	MFCD00056701
PubChem Substance ID:	329799772
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fenbufen may be used as an analytical reference standard for the quantification of the analyte in biological samples and pharmaceutical formulations using chromatography techniques.

5, 10 g in glass bottle

grade	analytical standard
Quality Level	100
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	184-187 °C (lit.)
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	OC(=O)CCC(=O)c1ccc(cc1)-c2ccccc2
InChI	1S/C16H14O3/c17-15(10-11-16(18)19)14-8-6-13(7-9-14)12-4-2-1-3-5-12/h1-9H,10-11H2,(H,18,19)
InChI key	ZPAKPRAICRBAOD-UHFFFAOYSA-N
Gene Information	human ... MMP2(4313), MMP3(4314), MMP9(4318)

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Fenofibrate is a third-generation fibric acid derivative which is widely employed for the treatment of atherogenic dyslipidemia, hypertriglyceridemia, mixed dyslipidemia and hypercholesterolemia.

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P301 + P310
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Fenofibrate

Empirical Formula (Hill Notation):	C₂₀H₂₁ClO₄
CAS Number:	49562-28-9
Molecular Weight:	360.83
EC Number:	256-376-3
MDL number:	MFCD00133314
PubChem Substance ID:	329823250
NACRES:	NA.24

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Fenofibrate may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by various chromatography and spectrophotometry techniques.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

To see an example of a Certificate of Analysis for this material enter LRAC0257 in the slot below. This is an example certificate only and may not be the lot that you receive.

Footnote

Quality Level	300
grade	certified reference material, pharmaceutical secondary standard
form	neat
CofA	current certificate can be downloaded
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to PhEur F0048000, traceable to USP 1269447
SMILES string	CC(C)OC(=O)C(C)(C)Oc1ccc(cc1)C(=O)c2ccc(Cl)cc2
InChI	1S/C20H21ClO4/c1-13(2)24-19(23)20(3,4)25-17-11-7-15(8-12-17)18(22)14-5-9-16(21)10-6-14/h5-13H,1-4H3
InChI key	YMTINGFKWWXKFG-UHFFFAOYSA-N
Gene Information	human ... PPARA(5465)

Fenofibric acid may be used as a reference standard in the determination of fenofibric acid in samples of human plasma using high performance liquid chromatography (HPLC) and liquid chromatography coupled with tandem mass spectrometry (LC-MS-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

hcodes	H412
pcodes	P273 - P501
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Fenofibric acid

Empirical Formula (Hill Notation):	C₁₇H₁₅ClO₄
CAS Number:	42017-89-0
Molecular Weight:	318.75
Beilstein/REAXYS Number:	2058973
EC Number:	255-626-9
MDL number:	MFCD00792461
PubChem Substance ID:	329769927
NACRES:	NA.24

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	1.0% water
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	O=C(C1=CC=C(OC(C)(C)C(O)=O)C=C1)C2=CC=C(Cl)C=C2
InChI	1S/C17H15ClO4/c1-17(2,16(20)21)22-14-9-5-12(6-10-14)15(19)11-3-7-13(18)8-4-11/h3-10H,1-2H3,(H,20,21)
InChI key	MQOBSOSZFYZQOK-UHFFFAOYSA-N
Gene Information	human ... PPARA(5465)

Fenoprofen calcium salt hydrate may be used as an analytical reference standard for the quantification of the analyte in environmental samples using gas chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H302 - H410
pcodes	P264 - P270 - P273 - P301 + P312 - P391 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3

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Fenoprofen calcium salt hydrate

Empirical Formula (Hill Notation):	C₃₀H₂₆CaO₆
Linear Formula:	C₃₀H₂₆O₆Ca
CAS Number:	53746-45-5
Molecular Weight:	522.60
EC Number:	252-107-9
MDL number:	MFCD00242722
PubChem Substance ID:	329799683
NACRES:	NA.24

5, 10 g in glass bottle

Quality Level	100
grade	analytical standard, for drug analysis
assay	97% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	O.[Ca].CC(C(O)=O)c1cccc(Oc2ccccc2)c1
InChI	1S/C15H14O3.Ca.H2O.2H/c1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13;;;;/h2-11H,1H3,(H,16,17);;1H2;;
InChI key	JWCQUXFJNIIYQZ-UHFFFAOYSA-N

Finasteride may be used as an analytical reference standard for the determination of the analyte in biological fluids and pharmaceutical formulations by high performance liquid chromatography (HPLC) method.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07
signalword	Warning
hcodes	H302 + H312 + H332
pcodes	P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Finasteride

Empirical Formula (Hill Notation):	C₂₃H₃₆N₂O₂
CAS Number:	98319-26-7
Molecular Weight:	372.54
MDL number:	MFCD00869737
PubChem Substance ID:	329754889

Biochem/physiol Actions

Selective 5α-reductase inhibitor; antiandrogen.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
SMILES string	[H][C@@]12CC[C@@]3([H])[C@]4([H])CC[C@H](C(=O)NC(C)(C)C)[C@@]4(C)CC[C@]3([H])[C@@]1(C)C=CC(=O)N2
InChI	1S/C23H36N2O2/c1-21(2,3)25-20(27)17-8-7-15-14-6-9-18-23(5,13-11-19(26)24-18)16(14)10-12-22(15,17)4/h11,13-18H,6-10,12H2,1-5H3,(H,24,26)(H,25,27)/t14-,15-,16-,17+,18+,22-,23+/m0/s1
InChI key	DBEPLOCGEIEOCV-WSBQPABSSA-N
Gene Information	human ... SRD5A2(6716)

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H360FD
pcodes	P201 - P202 - P264 - P270 - P301 + P312 - P308 + P313
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fipexide hydrochloride

Empirical Formula (Hill Notation):	C₂₀H₂₁ClN₂O₄ · HCl
CAS Number:	34161-24-5
Molecular Weight:	425.31
EC Number:	251-857-4
MDL number:	MFCD00133323
PubChem Substance ID:	329799752
NACRES:	NA.24

5 g in poly bottle

grade	analytical standard
Quality Level	200
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	Cl.Clc1ccc(OCC(=O)N2CCN(CC2)Cc3ccc4OCOc4c3)cc1
InChI	1S/C20H21ClN2O4.ClH/c21-16-2-4-17(5-3-16)25-13-20(24)23-9-7-22(8-10-23)12-15-1-6-18-19(11-15)27-14-26-18;/h1-6,11H,7-10,12-14H2;1H
InChI key	MVOWQBJZZKOQNU-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Firocoxib

Empirical Formula (Hill Notation):	C₁₇H₂₀O₅S
CAS Number:	189954-96-9
Molecular Weight:	336.40
Beilstein/REAXYS Number:	8335837
MDL number:	MFCD09837800
PubChem Substance ID:	329754109
NACRES:	NA.24

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	O=S(C1=CC=C(C2=C(OCC3CC3)C(OC2(C)C)=O)C=C1)(C)=O
InChI	1S/C17H20O5S/c1-17(2)14(12-6-8-13(9-7-12)23(3,19)20)15(16(18)22-17)21-10-11-4-5-11/h6-9,11H,4-5,10H2,1-3H3
InChI key	FULAPETWGIGNMT-UHFFFAOYSA-N

Flubendazole-d3 is an isotopically labeled compound of benzimidazole derivative, flubendazole.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

192,99 € / 18 139 ₽

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Flubendazole-d3

Empirical Formula (Hill Notation):	C₁₆D₃H₉FN₃O₃
CAS Number:	1173021-08-3
Molecular Weight:	316.30
MDL number:	MFCD11975215
PubChem Substance ID:	329754353
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Flubendazole-d3 may be used as an internal standard for the determination of flubendazole in animal muscle tissues and sludge samples by ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS).

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
mass shift	M+3
SMILES string	[2H]C([2H])([2H])OC(=O)Nc1nc2cc(ccc2[nH]1)C(=O)c3ccc(F)cc3
InChI	1S/C16H12FN3O3/c1-23-16(22)20-15-18-12-7-4-10(8-13(12)19-15)14(21)9-2-5-11(17)6-3-9/h2-8H,1H3,(H2,18,19,20,22)/i1D3
InChI key	CPEUVMUXAHMANV-FIBGUPNXSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 2

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Flucloxacillin sodium

Empirical Formula (Hill Notation):	C₁₉H₁₆ClFN₃NaO₅S
CAS Number:	1847-24-1
Molecular Weight:	475.85
EC Number:	217-428-0
MDL number:	MFCD01682108
PubChem Substance ID:	329754152
NACRES:	NA.24

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
storage temp.	2-8°C
SMILES string	CC1(C)[C@H](C([O-])=O)N2C([C@@H](NC(C3=C(C)ON=C3C4=C(F)C=CC=C4Cl)=O)[C@@]2([H])S1)=O.[Na+]
InChI	1S/C19H17ClFN3O5S.Na/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);/q;+1/p-1/t13-,14+,17-;/m1./s1
InChI key	OTEANHMVDHZOPB-SLINCCQESA-M

Flufenamic acid, a non-steroidal anti-inflammatory drug, is an effective analgesic agent.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Flufenamic acid

Empirical Formula (Hill Notation):	C₁₄H₁₀F₃NO₂
Linear Formula:	2-(CF₃C₆H₄NH)C₆H₄CO₂H
CAS Number:	530-78-9
Molecular Weight:	281.23
EC Number:	208-494-1
MDL number:	MFCD00002422
PubChem Substance ID:	329799777
NACRES:	NA.24

Flufenamic acid has been used as a standard in studying the two well defined, polymorphs of flufenamic acid like form I and form III, using solid-state density functional theory and terahertz spectroscopy.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard, for drug analysis
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	132-135 °C (lit.)
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	OC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F
InChI	1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)
InChI key	LPEPZBJOKDYZAD-UHFFFAOYSA-N