Supelco

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

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	100-102 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	CN(C)c1ccc(cc1)C(c2ccccc2)c3ccc(cc3)N(C)C
InChI	1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3
InChI key	WZKXBGJNNCGHIC-UHFFFAOYSA-N

Leucomalachite Green-d5 may be used as an internal standard for the determination of the triphenylmethane dye residues in rainbow trouts by liquid chromatography-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.

pictograms	GHS08
signalword	Warning
hcodes	H341 - H351
pcodes	P201 - P308 + P313
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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Leucomalachite Green-d5

Empirical Formula (Hill Notation):	C₂₃H₂₁D₅N₂
Linear Formula:	C₆D₅CH[C₆H₄N(CH₃)₂]₂
CAS Number:	947601-82-3
Molecular Weight:	335.50
MDL number:	MFCD06656251
PubChem Substance ID:	329754871
NACRES:	NA.24

grade	analytical standard
Quality Level	100
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 Environmental Food and Beverages Personal Care
format	neat
mass shift	M+5
SMILES string	[2H]c1c([2H])c([2H])c(c([2H])c1[2H])C(c2ccc(cc2)N(C)C)c3ccc(cc3)N(C)C
InChI	1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3/i5D,6D,7D,8D,9D
InChI key	WZKXBGJNNCGHIC-CFEWMVNUSA-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,GHS09
signalword	Warning
hcodes	H302 - H400
pcodes	P273 - P301 + P312 + P330
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Leucomalachite Green-d6

Empirical Formula (Hill Notation):	C₂₃D₆H₂₀N₂
Linear Formula:	C₆D₅CD[C₆H₄N(CH₃)₂]₂
CAS Number:	1173021-13-0
Molecular Weight:	336.50
MDL number:	MFCD09753325
PubChem Substance ID:	329754704
NACRES:	NA.24

grade	analytical standard
Quality Level	100
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 Environmental Food and Beverages Personal Care
format	neat
mass shift	M+6
SMILES string	[2H]c1c([2H])c([2H])c(c([2H])c1[2H])C([2H])(c2ccc(cc2)N(C)C)c3ccc(cc3)N(C)C
InChI	1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3/i5D,6D,7D,8D,9D,23D
InChI key	WZKXBGJNNCGHIC-OOBYGUTHSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Leucomycin hydrate may be used as an analytical reference standard for the determination of the veterinary drug in milk and meat samples by ultrahigh-performance liquid chromatography-tandem mass spectrometry.

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H302 - H400
pcodes	P273 - P301 + P312 + P330
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Leucomycin hydrate

CAS Number:	1392-21-8
MDL number:	MFCD00147435
NACRES:	NA.24

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
storage temp.	2-8°C

Levetiracetam is an orally active antiepileptic drug, having a high therapeutic index and potential antiepileptogenic and anticonvulsant effects.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
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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Levetiracetam

Empirical Formula (Hill Notation):	C₈H₁₄N₂O₂
CAS Number:	102767-28-2
Molecular Weight:	170.21
MDL number:	MFCD03265610
PubChem Substance ID:	329768167
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.
Levetiracetam may be used as a reference standard in the determination of levetiracetam in biological fluid samples using high-performance liquid chromatography coupled with electrospray tandem mass spectrometry (HPLC-ESI-MS/MS).

Levetiracetam is a pyrrolidine with antiepileptic activity. Stereoselective binding of levetiracetam was confined to synaptic plasma membranes in the central nervous system with no binding occurring in peripheral tissue. Levetiracetam inhibits burst firing without affecting normal neuronal excitability, which suggests that it may selectively prevent hyper-synchronization of epileptiform burst firing and propagation of seizure activity.

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
optical activity	[]/D -90±5°, c = 1 in acetone
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	CC[C@H](N1CCCC1=O)C(N)=O
InChI	1S/C8H14N2O2/c1-2-6(8(9)12)10-5-3-4-7(10)11/h6H,2-5H2,1H3,(H2,9,12)/t6-/m0/s1
InChI key	HPHUVLMMVZITSG-LURJTMIESA-N
Gene Information	human ... CACNA1B(774), SV2A(9900)

Chemical structure: quinolone

pictograms	GHS07
signalword	Warning
hcodes	H302 - H319
pcodes	P301 + P312 + P330 - P305 + P351 + P338
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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Levofloxacin

Empirical Formula (Hill Notation):	C₁₈H₂₀FN₃O₄
CAS Number:	100986-85-4
Molecular Weight:	361.37
Beilstein/REAXYS Number:	7327015
MDL number:	MFCD00865049
PubChem Substance ID:	329756033

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.

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
optical activity	[]20/D -104±4° in chloroform
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) Veterinary
format	neat
SMILES string	OC(C(C1=O)=CN2C(C1=CC(F)=C3N4CCN(C)CC4)=C3OC[C@@H]2C)=O
InChI	1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m0/s1
InChI key	GSDSWSVVBLHKDQ-JTQLQIEISA-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.
Lidocaine is a local anesthetic drug that can exhibit pronounced antiarrhythmic and anticonvulsant effects. It is known as a central nervous system depressant and shows sedative, analgesic and anticonvulsant properties.
Lidocaine is a drug, which serves as a potential candidate in the treatment of cardiac arrhythmias.
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.

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H317 - H334
pcodes	P261 - P264 - P270 - P280 - P301 + P312 - P302 + P352
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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Lidocaine

Empirical Formula (Hill Notation):	C₁₄H₂₂N₂O
CAS Number:	137-58-6
Molecular Weight:	234.34
EC Number:	205-302-8
MDL number:	MFCD00026733
PubChem Substance ID:	329823064
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.
Lidocaine may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by chromatography techniques.
Lidocaine may be used as an internal standard in the determination of perhexiline in human serum samples using gas liquid chromatography (GLC).

Na+ channel blocker; class IB antiarrhythmic that is rapidly absorbed after parenteral administration.

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

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.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAC0142 in the slot below. This is an example certificate only and may not be the lot that you receive.

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	Cleaning Products Cosmetics Food and Beverages Personal Care Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to BP 727, traceable to PhEur L0595000, traceable to USP 1366002
SMILES string	CCN(CC)CC(=O)Nc1c(C)cccc1C
InChI	1S/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)
InChI key	NNJVILVZKWQKPM-UHFFFAOYSA-N
Gene Information	human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

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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Lidocaine hydrochloride

Empirical Formula (Hill Notation):	C₁₄H₂₂N₂O · HCl · H₂O
CAS Number:	6108-05-0
Molecular Weight:	288.81
EC Number:	200-803-8
MDL number:	MFCD00150329
PubChem Substance ID:	329823258
NACRES:	NA.24

Na+ channel blocker; class IB antiarrhythmic that is rapidly absorbed after parenteral administration

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 LRAB3669 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 BP 214, traceable to PhEur L0600000, traceable to USP 1366002
SMILES string	Cl[H].[H]O[H].CCN(CC)CC(=O)Nc1c(C)cccc1C
InChI	1S/C14H22N2O.ClH.H2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4;;/h7-9H,5-6,10H2,1-4H3,(H,15,17);1H;1H2
InChI key	YECIFGHRMFEPJK-UHFFFAOYSA-N
Gene Information	human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

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

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P301 + P330 + P331 + P310
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Lidocaine-(diethyl-d10)

Empirical Formula (Hill Notation):	C₁₄D₁₀H₁₂N₂O
CAS Number:	851528-09-1
Molecular Weight:	244.40
MDL number:	MFCD06658679
PubChem Substance ID:	329755903
NACRES:	NA.24

LC-MS identity conforms

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
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
storage temp.	2-8°C
SMILES string	O=C(CN(C([2H])([2H])C([2H])([2H])[2H])C([2H])([2H])C([2H])([2H])[2H])NC1=C(C)C=CC=C1C
InChI	1S/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)/i1D3,2D3,5D2,6D2
InChI key	NNJVILVZKWQKPM-JKSUIMTKSA-N

Certan Vial
Linalool is a principle monoterpene component present in many essential oils of aromatic species, which possess anti-inflammatory property and hence can be used to cure a variety of ailments, found to be both acute and chronic.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
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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Linalool

Empirical Formula (Hill Notation):	C₁₀H₁₈O
Linear Formula:	(CH₃)₂C=CHCH₂CH₂C(CH₃)(OH)CH=CH₂
CAS Number:	78-70-6
Molecular Weight:	154.25
Beilstein/REAXYS Number:	1721488
EC Number:	201-134-4
MDL number:	MFCD00008906
PubChem Substance ID:	329757741

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 pressure	0.17 mmHg ( 25 °C)
assay	99.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.462 (lit.)
bp	194-197 °C/720 mmHg (lit.)
density	0.87 g/mL at 25 °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	C\C(C)=C\CCC(C)(O)C=C
InChI	1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3
InChI key	CDOSHBSSFJOMGT-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
signalword	Warning
hcodes	H315 - H317 - H319
pcodes	P261 - P264 - P272 - P280 - P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	NA 1993 / PGIII
WGK Germany	WGK 1

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Linalyl acetate

Empirical Formula (Hill Notation):	C₁₂H₂₀O₂
Linear Formula:	CH₃CO₂C(CH=CH₂)(CH₃)CH₂CH₂CH=C(CH₃)₂
CAS Number:	115-95-7
Molecular Weight:	196.29
Beilstein/REAXYS Number:	1724500
EC Number:	204-116-4
MDL number:	MFCD00008907
PubChem Substance ID:	329757483
NACRES:	NA.24

Quality Level	100
grade	analytical standard
vapor density	6.8 (vs air)
vapor pressure	0.1 mmHg ( 20 °C)
assay	97.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.453 (lit.)
bp	220 °C (lit.)
density	1.448-1.452 at 20 °C, 0.901 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Flavors and Fragrances Food and Beverages Personal Care
format	neat
storage temp.	2-8°C
SMILES string	C\C(C)=C\CCC(C)(OC(C)=O)C=C
InChI	1S/C12H20O2/c1-6-12(5,14-11(4)13)9-7-8-10(2)3/h6,8H,1,7,9H2,2-5H3
InChI key	UWKAYLJWKGQEPM-UHFFFAOYSA-N

Chemical structure: aminoglycoside
Lincomycin hydrochloride monohydrate, an antibiotic used in treating infections caused by staphylococcal, streptococcal, and Bacteroides fragilis. It is produced by Streptomyces lincolnensis.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H317 - H319
pcodes	P261 - P264 - P272 - P280 - P302 + P352 - P305 + P351 + P338
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 1
Flash Point F	201.2 °F - closed cup
Flash Point C	94 °C - closed cup

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Lincomycin hydrochloride monohydrate

Empirical Formula (Hill Notation):	C₁₈H₃₄N₂O₆S · HCl · H₂O
CAS Number:	7179-49-9
Molecular Weight:	461.01
EC Number:	212-726-7
MDL number:	MFCD00167245
PubChem Substance ID:	329753904
NACRES:	NA.24

Lincomycin HCl monohydrate may have been used as reference standard for determination of antibiotics in novel tablet formulation using HPLC.
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
storage temp.	2-8°C
SMILES string	Cl[H].[H]O[H].CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@@H](C)O)[C@H]2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O
InChI	1S/C18H34N2O6S.ClH.H2O/c1-5-6-10-7-11(20(3)8-10)17(25)19-12(9(2)21)16-14(23)13(22)15(24)18(26-16)27-4;;/h9-16,18,21-24H,5-8H2,1-4H3,(H,19,25);1H;1H2/t9-,10-,11+,12-,13+,14-,15-,16-,18-;;/m1../s1
InChI key	LFZGYTBWUHCAKF-DCNJEFSFSA-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
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
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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Lipoic acid, reduced

Empirical Formula (Hill Notation):	C₈H₁₆O₂S₂
CAS Number:	462-20-4
Molecular Weight:	208.34
MDL number:	MFCD00166974
PubChem Substance ID:	329826876
NACRES:	NA.24

25, 100 mg in ampule
1 g in ampule
Sealed ampule.

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. T8260.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

grade	analytical standard
Quality Level	100
assay	98%
form	liquid
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Forensics and Toxicology Personal Care Veterinary
format	neat
SMILES string	OC(=O)CCCCC(S)CCS
InChI	1S/C8H16O2S2/c9-8(10)4-2-1-3-7(12)5-6-11/h7,11-12H,1-6H2,(H,9,10)
InChI key	IZFHEQBZOYJLPK-UHFFFAOYSA-N

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

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H317 - H318 - H411
pcodes	P261 - P273 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	348.1 °F - Cleveland open cup
Flash Point C	175.6 °C - Cleveland open cup

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Lithium Standard for IC

1000 mg/L Li+ in 0.1% nitric acid, prepared with high purity Li2CO3, HNO3 and water

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

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L Li⁺ in nitric acid
application(s)	ion chromatography: suitable
Featured Industry	Environmental Food and Beverages
format	single component solution

Lithol Rubine BK (E-180) is a red mono azo dye, authorized as a food additive by the European Union. It belongs to the class of food dyes, which are used to give colorless foodstuffs a more characteristic appearance as well as to change the original colors to preferred artificial ones. E-180 is reported to be used in edible cheese rind, following the Quantum Satis (QS) principle.
This product is provided by Sigma-Aldrich as a neat standard for the precise quality control of food products. In the European Union, E numbers are used as codes for food color additives. E numbers 100-199 include not only artificial food colors derived from petroleum, but also natural additives originating from sources such as vegetables, insects, or mixtures made from natural foodstuffs.

Personal Protective Equipment	Eyeshields, Faceshields, Gloves
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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Lithol Rubine BK

Empirical Formula (Hill Notation):	C₁₈H₁₂CaN₂O₆S
CAS Number:	5281-04-9
Molecular Weight:	424.44
Colour Index Number:	15850
EC Number:	226-109-5
E Number:	E180
NACRES:	NA.24

Lithol Rubine BK may be used as a chelating agent for the determination of mercury (II) in water samples by spectrophotometric method.
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	95.0% (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	[Ca++].Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C([O-])=O)c(c1)S([O-])(=O)=O
InChI	1S/C18H14N2O6S.Ca/c1-10-6-7-14(15(8-10)27(24,25)26)19-20-16-12-5-3-2-4-11(12)9-13(17(16)21)18(22)23;/h2-9,19H,1H3,(H,22,23)(H,24,25,26);/q;+2/p-2/b20-16-;
InChI key	WANIKCLUTOABTP-LRZQPWDCSA-L

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 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Loganin

Empirical Formula (Hill Notation):	C₁₇H₂₆O₁₀
CAS Number:	18524-94-2
Molecular Weight:	390.38
Beilstein/REAXYS Number:	55724
EC Number:	242-398-0
MDL number:	MFCD00075645
PubChem Substance ID:	329755352
NACRES:	NA.24

Bottomless glass bottle. Contents are inside inserted fused cone.

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 36483.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Iridoid glycoside isolated from various plants. Substrate for cytochrome P450

grade	analytical standard
Quality Level	100
assay	≥97.0% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
SMILES string	COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]3[C@@H](C)[C@@H](O)C[C@H]13
InChI	1S/C17H26O10/c1-6-9(19)3-7-8(15(23)24-2)5-25-16(11(6)7)27-17-14(22)13(21)12(20)10(4-18)26-17/h5-7,9-14,16-22H,3-4H2,1-2H3/t6-,7+,9-,10+,11+,12+,13-,14+,16-,17-/m0/s1
InChI key	AMBQHHVBBHTQBF-UOUCRYGSSA-N

Lupeol is a novel anti-cancer and anti-inflammatory dietary triterpene. They help in stabilizing phospholipid bilayers in plant cell membranes. In general, this group contains 28-29 carbons along with carbon-carbon double bonds, usually one in the sterol nucleus and at times a second in the alkyl side chain.

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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Lupeol

Empirical Formula (Hill Notation):	C₃₀H₅₀O
CAS Number:	545-47-1
Molecular Weight:	426.72
EC Number:	208-889-9
MDL number:	MFCD00017351
PubChem Substance ID:	329751732
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.
It was used as reference standard in method development and validation of lupeol from Vernonia Cinerea using HPLC method.

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
assay	≥90.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	[H]C12CCC3C4(C)CCC(O)C(C)(C)[C@]4([H])CCC3(C)[C@]1(C)CCC5(C)CC[C@H](C(C)=C)[C@]25[H]
InChI	1S/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21+,22-,23+,24-,25+,27+,28-,29+,30+/m0/s1
InChI key	MQYXUWHLBZFQQO-QGTGJCAVSA-N

Luteolin is a naturally occurring flavone, readily present in vegetables. It may possess many biological properties like anti-tumor activity against condition of skin papilloma.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
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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Luteolin

Empirical Formula (Hill Notation):	C₁₅H₁₀O₆
CAS Number:	491-70-3
Molecular Weight:	286.24
Beilstein/REAXYS Number:	292084
EC Number:	207-741-0
MDL number:	MFCD00017309
PubChem Substance ID:	329764132

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.

Quality Level	100
grade	analytical standard
assay	≥97.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	~330 °C (lit.)
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	Oc1cc(O)c2C(=O)C=C(Oc2c1)c3ccc(O)c(O)c3
InChI	1S/C15H10O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-6,16-19H
InChI key	IQPNAANSBPBGFQ-UHFFFAOYSA-N

Luteolin 7-glucoside is a naturally occurring flavanoid isolated from Reseda luteola L.

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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Luteolin 7-glucoside

Empirical Formula (Hill Notation):	C₂₁H₂₀O₁₁
CAS Number:	5373-11-5
Molecular Weight:	448.38
EC Number:	226-365-8
MDL number:	MFCD06799436
PubChem Substance ID:	329757550
NACRES:	NA.24

Luteolin 7-glucoside may be used as an analytical reference standard for the quantification of the anayte in Olea europaea leaves using high-performance liquid chromatography (HPLC).
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.

Quality Level	100
grade	analytical standard
assay	≥98% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	OC[C@H]1O[C@@H](Oc2cc(O)c3C(=O)C=C(Oc3c2)c4ccc(O)c(O)c4)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1
InChI key	PEFNSGRTCBGNAN-QNDFHXLGSA-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 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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m-Chloramphenicol

Empirical Formula (Hill Notation):	C₁₁H₁₂Cl₂N₂O₅
CAS Number:	7411-65-6
Molecular Weight:	323.13
MDL number:	MFCD07370152
PubChem Substance ID:	329754750

Mode of Action: Chloramphenicol inhibits bacterial protein synthesis by blocking the peptidyl transferase step by binding to the 50S ribosomal subunit and preventing attachment of aminoacyl tRNA to the ribosome. It also inhibits mitochondrial and chloroplast protein synthesis and ribosomal formation of (p)ppGpp, de-pressing rRNA transcription.
Mode of Resistance: Use of chloramphenicol acetyltransferase will acetylate the product and inactivate it.
Antimicrobial Spectrum: This is a broad spectrum antibiotic against gram-positive and gram-negative bacteria, and is used mainly for ophthalmic and veterinary purposes.

Caution

Stock solutions should be stored at 2-8°C and are stable at 37°C for 5 days. Aqueous solutions are neutral and stable over a wide pH range, with 50% hydrolysis occurring after 290 days. Use of a borax buffered solution reduces this number to 14%. Solutions should be protected from light as photochemical decomposition results in a yellowing of the solution. Heating aqueous solutions at 115°C for 30 minutes results in a 10% loss of chloramphenicol.

Preparation Note

Stock solutions can be prepared directly in the vial at any recommended concentration. A solution at 50 mg/mL in ethanol yields a clear, very faint, yellow solution. Degradation of chloramphenicol in aqueous solution is catalyzed by general acids and bases. This rate of degradation is independent of the ionic strength and pH.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
description	threo-form
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable, solid phase extraction (SPE): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1cccc(c1)[N+]([O-])=O
InChI	1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-2-1-3-7(4-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)/t8-,9-/m1/s1
InChI key	FTMJFHVKAXPFIY-RKDXNWHRSA-N

m-Cresol is an isomer form of Cresol and is mainly used as an intermediate in the manufacture of chemicals. It is toxic in nature. It is a component of coal tar creosote which is used for wood preservation. It also possess bactericide and fungicide property.

pictograms	GHS08
signalword	Danger
hcodes	H350
pcodes	P201 - P202 - P280 - P308 + P313 - P405 - P501
Personal Protective Equipment	Eyeshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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m-Cresol

Empirical Formula (Hill Notation):	C₇H₈O
Linear Formula:	CH₃C₆H₄OH
CAS Number:	108-39-4
Molecular Weight:	108.14
Beilstein/REAXYS Number:	506719
EC Number:	203-577-9
MDL number:	MFCD00002302
PubChem Substance ID:	329760142
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.
It was used as reference standard solution for determination of phenolic compounds in tyrosinase biosensor using amperometric detection under self-assembled monolayers-based bioelectrode flow-injection.

Quality Level	100
grade	analytical standard
vapor density	3.72 (vs air)
vapor pressure	<1 mmHg ( 20 °C)
assay	99.0% (GC)
form	neat
autoignition temp.	1036 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	1.06-1.35 %, 150 °F
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.541 (lit.), n20/D 1.542
bp	203 °C (lit.)
mp	8-10 °C (lit.)
density	1.034 g/mL at 25 °C (lit.)
Featured Industry	Agriculture Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	Cc1cccc(O)c1
InChI	1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3
InChI key	RLSSMJSEOOYNOY-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,GHS06
signalword	Danger
hcodes	H301 + H311 - H314 - H412
pcodes	P270 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Personal Protective Equipment	Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
RIDADR	UN 2076 8(6.1) / PGII
WGK Germany	WGK 2
Flash Point F	186.8 °F - closed cup
Flash Point C	86 °C - closed cup

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m-Cymene

Empirical Formula (Hill Notation):	C₁₀H₁₄
Linear Formula:	CH₃C₆H₄CH(CH₃)₂
CAS Number:	535-77-3
Molecular Weight:	134.22
Beilstein/REAXYS Number:	1851357
EC Number:	208-617-9
MDL number:	MFCD00008891
PubChem Substance ID:	329753412
NACRES:	NA.24

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
vapor pressure	4 mmHg ( 37.7 °C)
assay	98.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.492 (lit.), n20/D 1.493
bp	175 °C (lit.)
mp	64 °C (lit.)
density	0.861 g/mL at 25 °C (lit.)
Featured Industry	Environmental Food and Beverages
format	neat
SMILES string	CC(C)c1cccc(C)c1
InChI	1S/C10H14/c1-8(2)10-6-4-5-9(3)7-10/h4-8H,1-3H3
InChI key	XCYJPXQACVEIOS-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
signalword	Warning
hcodes	H226
pcodes	P210
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2046 3 / PGIII
WGK Germany	WGK 2
Flash Point F	116.6 °F - closed cup
Flash Point C	47 °C - closed cup

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m-Terphenyl

Empirical Formula (Hill Notation):	C₁₈H₁₄
Linear Formula:	C₆H₅C₆H₄C₆H₅
CAS Number:	92-06-8
Molecular Weight:	230.30
Beilstein/REAXYS Number:	1864778
EC Number:	202-122-1
MDL number:	MFCD00003059
PubChem Substance ID:	329756961
NACRES:	NA.24

Quality Level	100
grade	analytical standard
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	379 °C (lit.)
mp	84-88 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	c1ccc(cc1)-c2cccc(c2)-c3ccccc3
InChI	1S/C18H14/c1-3-8-15(9-4-1)17-12-7-13-18(14-17)16-10-5-2-6-11-16/h1-14H
InChI key	YJTKZCDBKVTVBY-UHFFFAOYSA-N

m-Xylene is an aromatic liquid , which is an isomeric form of xylene.
m-Xylene is an aromatic liquid, which is an isomeric form of xylene.
m-Xylene is an environmental pollutant belonging to the class of volatile organic compounds. It is emitted from a variety of sources including adhesives, degreasing agents, combustion products of wood and fuels, industrial paints, aerosols, etc.

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H315 - H319 - H335 - H400
pcodes	P273 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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m-Xylene

Empirical Formula (Hill Notation):	C₈H₁₀
Linear Formula:	C₆H₄(CH₃)₂
CAS Number:	108-38-3
Molecular Weight:	106.17
Beilstein/REAXYS Number:	605441
EC Number:	203-576-3
MDL number:	MFCD00008536
PubChem Substance ID:	329770476
NACRES:	NA.24

m-Xylene may be used as an analytical reference standard for the quantification of the analyte in occupational environmental samples and groundwater samples using gas chromatography technique with different modes of detection.
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	3.7 (vs air)
assay	99.5% (GC)
form	neat
autoignition temp.	982 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	7 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.497 (lit.), n20/D 1.497
bp	138-139 °C (lit.)
mp	48 °C (lit.)
density	0.868 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	Cc1cccc(C)c1
InChI	1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3
InChI key	IVSZLXZYQVIEFR-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,GHS08
signalword	Danger
hcodes	H226 - H304 - H312 + H332 - H315 - H319 - H335 - H412
pcodes	P210 - P273 - P280 - P301 + P310 - P303 + P361 + P353 - P331
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1307 - class 3 - PG 3 - Xylenes
WGK Germany	WGK 2
Flash Point F	80.6 °F - closed cup
Flash Point C	27 °C - closed cup

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m-Xylene solution

CAS Number:	108-38-3
EC Number:	203-576-3

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
InChI	1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3
InChI key	IVSZLXZYQVIEFR-UHFFFAOYSA-N

Malachite green chloride is a triphenylmethane dye, which generally can find applications in aquaculture and highly effective against fungal infections.
Malachite Green chloride (MG), a neat reference standard, is provided for the analyte detection, food color quality, and safety control of your products! Malachite Green is a low-cost, highly efficient, cationic triphenylmethane dye with high efficacy for treating fungal, bacterial, and parasitic infections. MG is also employed in paper, textile, acrylic industries, and as an anthelmintic agent, food and color additive, medical disinfectant, etc.

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	UN1307 - class 3 - PG 3 - Xylenes
WGK Germany	WGK 2
Flash Point F	51.8 °F - closed cup
Flash Point C	11 °C - closed cup

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Malachite Green chloride

Empirical Formula (Hill Notation):	C₂₃H₂₅ClN₂
CAS Number:	569-64-2
Molecular Weight:	364.91
Colour Index Number:	42000
Beilstein/REAXYS Number:	3580148
EC Number:	209-322-8
MDL number:	MFCD00011751
PubChem Substance ID:	329755786
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.
Malachite Green chloride may be used as an analytical standard to investigate its carcinogenic nature in the animal matrix. The techniques, proton nuclear magnetic resonance (1H), carbon-13 nuclear magnetic resonance (13C NMR), high-performance liquid chromatography (HPLC), and gas chromatography (GC) are used to confirm the identity of the material and to determine the purity of malachite green chloride.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	90% (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
SMILES string	[Cl-].CN(C)c1ccc(cc1)C(\c2ccccc2)=C3\C=CC(\C=C3)=[N+](\C)C
InChI	1S/C23H25N2.ClH/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4;/h5-17H,1-4H3;1H/q+1;/p-1
InChI key	FDZZZRQASAIRJF-UHFFFAOYSA-M

Malachite Green-d5 picrate is an isotopically labeled analog of the triphenylmethane dye, malachite green (MG).

pictograms	GHS05,GHS07,GHS08,GHS09
signalword	Danger
hcodes	H302 - H318 - H361d - H410
pcodes	P201 - P273 - P280 - P301 + P312 - P305 + P351 + P338 - P308 + P313
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Malachite Green-d5 picrate

Empirical Formula (Hill Notation):	C₂₉D₅H₂₂N₅O₇
CAS Number:	1258668-21-1
Molecular Weight:	562.58
PubChem Substance ID:	24860644
NACRES:	NA.24

Malachite Green-d5 picrate may be used as an internal standard for the quantification of malachite green in aquaculture products using liquid chromatography coupled to mass spectrometry operated in positive electrospray ionization mode (ESI+) and equipped with multiple reaction monitoring mode (MRM).
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	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
mass shift	M+5
SMILES string	[O-]c1c(cc(cc1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O.[2H]c2c([2H])c([2H])c(c([2H])c2[2H])\C(c3ccc(cc3)N(C)C)=C4\C=CC(\C=C4)=[N+](/C)C

1000 mg/L malate in water, prepared with L-(−)-malic acid and water; filtered through a 0.2 μm membrane filter and stabilized with sodium azide

pictograms	GHS02,GHS06
signalword	Danger
hcodes	H228 - H301
pcodes	P210 - P301 + P310 + P330
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges
RIDADR	UN 2926 6.1(4.1) / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Malate Standard for IC

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

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L malate in water
application(s)	ion chromatography: suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution

1000 mg/L maleate in water, prepared with maleic acid and water; filtered through a 0.2 μm membrane filter and stabilized with sodium azide

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

605,03 € / 56 865 ₽

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Maleate Standard for IC

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

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L maleate in water
application(s)	ion chromatography: suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution

pictograms	GHS07
signalword	Warning
hcodes	H317
pcodes	P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
RIDADR	NONH for all modes of transport
WGK Germany	nwg
Flash Point F	Not applicable
Flash Point C	Not applicable

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Malonate Standard for IC

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

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L malonate in water
application(s)	ion chromatography: suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution

Malvidin-3-galactoside chloride is an anthocyanin pigment found in magenta and dark red flowers of Primula polyanthus.

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

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Malvidin-3-galactoside chloride

Empirical Formula (Hill Notation):	C₂₃H₂₅ClO₁₂
CAS Number:	30113-37-2
Molecular Weight:	528.89
EC Number:	250-055-1
MDL number:	MFCD00185577
PubChem Substance ID:	329768395
NACRES:	NA.25

Malvidin-3-galactoside chloride is a type of fluorescent dye commonly used to identify glycerides and free fatty acids.

grade	analytical standard
Quality Level	100
assay	≥95% (HPLC)
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	[Cl-].COc1cc(cc(OC)c1O)-c2[o+]c3cc(O)cc(O)c3cc2O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O
InChI	1S/C23H24O12.ClH/c1-31-14-3-9(4-15(32-2)18(14)27)22-16(7-11-12(26)5-10(25)6-13(11)33-22)34-23-21(30)20(29)19(28)17(8-24)35-23;/h3-7,17,19-21,23-24,28-30H,8H2,1-2H3,(H2-,25,26,27);1H/t17-,19+,20+,21-,23-;/m1./s1
InChI key	YDIKCZBMBPOGFT-PWUSVEHZSA-N

1000 mg/L Mn2+ in 0.1% nitric acid, prepared with high purity Mn metal, HNO3 and water

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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Manganese Standard for IC

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

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L Mn⁺² in nitric acid
application(s)	ion chromatography: suitable
Featured Industry	Environmental Food and Beverages
format	single component solution

Mangiferin is a xanthone glucoside and a naturally occurring polyphenol found abundantly in the plants of genus Mangifera particularly Mangifera indica L. and also in some medicinal herbs. Mangiferin exhibits antioxidant, antiviral, antitumor, anti-inflammatory and gene-regulatory effects and is considered to be of high research interest due to its therapeutic properties.

Personal Protective Equipment	Eyeshields, Gloves
RIDADR	UN 3264 8 / PGIII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Mangiferin

Empirical Formula (Hill Notation):	C₁₉H₁₈O₁₁
CAS Number:	4773-96-0
Molecular Weight:	422.34
MDL number:	MFCD00075656
PubChem Substance ID:	329748228
NACRES:	NA.24

Mangiferin may be used as an analytical standard for the determination of the analyte in rat plasma, traditional Chinese medicines and honeybush tea (Cyclopia spp.) by chromatography based techniques.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	≥98.0% (TLC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c2c(O)cc3Oc4cc(O)c(O)cc4C(=O)c3c2O
InChI	1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2/t11-,15-,17+,18-,19+/m1/s1
InChI key	AEDDIBAIWPIIBD-ZJKJAXBQSA-N

Общее описание
Стандарт для картриджей Supelco MIP SPE. Для получения дополнительной информации обратитесь к документации Supelco T407075, T706019, T706030, T706020
Приложение
Для получения дополнительной информации о подходящей методике проведения анализа обратитесь к сертификату на изделие. Обратитесь в техническую службу для получения дополнительной поддержки.
Упаковка
Стеклянный флакон без дна. Содержимое находится внутри вставленного в него оплавленного конуса.
Юридическая информация
VETERAN является зарегистрированной торговой маркой Sigma-Aldrich Chemie GmbH.

pictograms	GHS06
signalword	Danger
hcodes	H300
pcodes	P264 - P270 - P301 + P310 - P405 - P501
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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Аналитический стандарт мапентерола гидрохлорид Supelco

Empirical Formula (Hill Notation):	C₁₄H₂₀ClF₃N₂O · HCl
CAS Number:	54238-51-6
Molecular Weight:	361.23
MDL number:	MFCD10567361
PubChem Substance ID:	329757445
NACRES:	NA.24

Кат. номер

49358-VAR

49358-5MG

Информация по технике безопасности

Уровень качества	100
Класс	аналитический стандарт
Линейка продуктов	VETRANAL^®
Анализ	98.5% (ВЭЖХ)
Форма	neat
Область применения	ВЭЖХ: подходит, газовая хроматография (GC): подходит, твердофазная экстракция (SPE): подходит
Избранная отрасль	Криминалистика и токсикология Фармацевтика (низкомолекулярная) Ветеринария
Формат	neat
Температура хранения	2-8°C
SMILES string	Cl.CCC(C)(C)NCC(O)c1cc(Cl)c(N)c(c1)C(F)(F)F
InChI	1S/C14H20ClF3N2O.ClH/c1-4-13(2,3)20-7-11(21)8-5-9(14(16,17)18)12(19)10(15)6-8;/h5-6,11,20-21H,4,7,19H2,1-3H3;1H
InChI key	LWJSGOMCMMDPEN-UHFFFAOYSA-N

Пиктограммы	GHS07
Сигнальное слово	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Целевые органы	Дыхательная система
Personal Protective Equipment	респиратор типа N95 (US), Защитные очки, Перчатки
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Непригодный
Flash Point C	Непригодный

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MDI-DBA Oligomers Standard CRM40603

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.

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	in methanol (varied conc.)
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	multi-component solution
storage temp.	2-8°C

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
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 1
Flash Point F	49.5 °F - closed cup
Flash Point C	9.7 °C - closed cup

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MDI-DBA-d9 Oligomers Standard CRM40604

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	in methanol (varied conc.)
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	multi-component solution
storage temp.	2-8°C

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

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
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 1
Flash Point F	49.5 °F - closed cup
Flash Point C	9.7 °C - closed cup

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Mebendazole

Empirical Formula (Hill Notation):	C₁₆H₁₃N₃O₃
CAS Number:	31431-39-7
Molecular Weight:	295.29
Beilstein/REAXYS Number:	759809
EC Number:	250-635-4
MDL number:	MFCD00057872
PubChem Substance ID:	329757164
NACRES:	NA.24

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)C(=O)c3ccccc3
InChI	1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)
InChI key	OPXLLQIJSORQAM-UHFFFAOYSA-N

Chemical structure: -lactam
Mecillinam is a beta-lactam antibiotic, specific to penicillin-binding protein 2 (PBP2) in Escherichia coli, which tends to block cell wall elongation and indirectly blocks cell division.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
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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Mecillinam

Empirical Formula (Hill Notation):	C₁₅H₂₃N₃O₃S
CAS Number:	32887-01-7
Molecular Weight:	325.43
EC Number:	251-277-1
MDL number:	MFCD00056869
PubChem Substance ID:	329754550
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
storage temp.	2-8°C
SMILES string	[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2\N=C\N3CCCCCC3)C(O)=O
InChI	1S/C15H23N3O3S/c1-15(2)11(14(20)21)18-12(19)10(13(18)22-15)16-9-17-7-5-3-4-6-8-17/h9-11,13H,3-8H2,1-2H3,(H,20,21)/b16-9+/t10-,11+,13-/m1/s1
InChI key	BWWVAEOLVKTZFQ-ISVUSNJMSA-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 2

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Medroxyprogesterone

Empirical Formula (Hill Notation):	C₂₂H₃₂O₃
CAS Number:	520-85-4
Molecular Weight:	344.49
Beilstein/REAXYS Number:	2510965
EC Number:	208-298-6
MDL number:	MFCD00069474
PubChem Substance ID:	329757167
NACRES:	NA.24

Caution

Much of the pharmacology literature refers to medroxyprogesterone acetate as medroxyprogesterone, but they are of course not the same substance.

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	Pharmaceutical (small molecule)
format	neat
SMILES string	[H][C@@]12C[C@H](C)C3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@@]4(C)[C@@]2([H])CC[C@]4(O)C(C)=O
InChI	1S/C22H32O3/c1-13-11-16-17(20(3)8-5-15(24)12-19(13)20)6-9-21(4)18(16)7-10-22(21,25)14(2)23/h12-13,16-18,25H,5-11H2,1-4H3/t13-,16+,17-,18-,20+,21-,22-/m0/s1
InChI key	FRQMUZJSZHZSGN-HBNHAYAOSA-N

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

pictograms	GHS08
signalword	Warning
hcodes	H361fd
pcodes	P201 - P202 - P280 - P308 + P313 - P405 - P501
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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Medroxyprogesterone 17-acetate

Empirical Formula (Hill Notation):	C₂₄H₃₄O₄
CAS Number:	71-58-9
Molecular Weight:	386.52
Beilstein/REAXYS Number:	2066112
EC Number:	200-757-9
MDL number:	MFCD00010483
PubChem Substance ID:	329757168
NACRES:	NA.24

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
mp	206-207 °C (lit.)
Featured Industry	Pharmaceutical (small molecule)
format	neat
SMILES string	[H][C@@]12C[C@H](C)C3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@@]4(C)[C@@]2([H])CC[C@]4(OC(C)=O)C(C)=O
InChI	1S/C24H34O4/c1-14-12-18-19(22(4)9-6-17(27)13-21(14)22)7-10-23(5)20(18)8-11-24(23,15(2)25)28-16(3)26/h13-14,18-20H,6-12H2,1-5H3/t14-,18+,19-,20-,22+,23-,24-/m0/s1
InChI key	PSGAAPLEWMOORI-PEINSRQWSA-N
Gene Information	human ... PGR(5241)

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
An NSAID. Circumvents MRP-mediated multidrug resistance. Specifically and significantly potentiates the cytotoxicity of anthracyclines (doxorubicin, daunorubicin and epirubicin), as well as teniposide, VP-16 and vincristine.

pictograms	GHS08
signalword	Warning
hcodes	H351 - H413
pcodes	P201 - P202 - P273 - P280 - P308 + P313 - P405
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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Mefenamic acid

Empirical Formula (Hill Notation):	C₁₅H₁₅NO₂
CAS Number:	61-68-7
Molecular Weight:	241.29
EC Number:	200-513-1
MDL number:	MFCD00051721
PubChem Substance ID:	329770141

Quality Level	100
grade	analytical standard
assay	98.5% (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) Veterinary
format	neat
SMILES string	Cc1cccc(Nc2ccccc2C(O)=O)c1C
InChI	1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)
InChI key	HYYBABOKPJLUIN-UHFFFAOYSA-N
Gene Information	human ... PTGS1(5742), PTGS2(5743)

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
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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Mefenamic acid-(benzoic ring-13C6)

Empirical Formula (Hill Notation):	¹³C₆C₉H₁₅NO₂
CAS Number:	1325559-19-0
Molecular Weight:	247.24
MDL number:	MFCD20036277
PubChem Substance ID:	329755133
NACRES:	NA.24

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)
format	neat
mass shift	M+6
SMILES string	Cc1cccc(N[13c]2[13cH][13cH][13cH][13cH][13c]2C(O)=O)c1C
InChI	1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)/i3+1,4+1,7+1,8+1,12+1,14+1
InChI key	HYYBABOKPJLUIN-MQISJZSBSA-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
signalword	Danger
hcodes	H315 - H318
pcodes	P280 - P305 + P351 + P338
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Mefexamide hydrochloride

Empirical Formula (Hill Notation):	C₁₅H₂₄N₂O₃ · HCl
CAS Number:	1227-61-8
Molecular Weight:	316.82
EC Number:	214-963-1
MDL number:	MFCD00079457
PubChem Substance ID:	329818058
NACRES:	NA.24

5 g in poly bottle

Quality Level	200
grade	analytical standard, for drug analysis
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	Cl.CCN(CC)CCNC(=O)COc1ccc(OC)cc1
InChI	1S/C15H24N2O3.ClH/c1-4-17(5-2)11-10-16-15(18)12-20-14-8-6-13(19-3)7-9-14;/h6-9H,4-5,10-12H2,1-3H3,(H,16,18);1H
InChI key	AXBHPHPHZHAOAK-UHFFFAOYSA-N

Megestrol acetate is a commonly used synthetically prepared glucosteroid, which possesses anti-inflammatory property.

pictograms	GHS06
signalword	Danger
hcodes	H300 + H310 + H330
pcodes	P260 - P262 - P264 - P280 - P302 + P352 + P310 - P304 + P340 + P310
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	UN 2811 6.1 / PGI
WGK Germany	WGK 3

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Megestrol acetate

Empirical Formula (Hill Notation):	C₂₄H₃₂O₄
CAS Number:	595-33-5
Molecular Weight:	384.51
Beilstein/REAXYS Number:	1917291
EC Number:	209-864-5
MDL number:	MFCD00056470
PubChem Substance ID:	329817798
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.
Megestrol acetate may be used as a reference standard for the determination of megestrol acetate in human serum using reversed-phase high performance liquid chromatography (RP-HPLC).

1, 5 g in poly bottle

Quality Level	100
grade	analytical standard, for drug analysis
assay	99% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	[H][C@]12CC[C@@]3(C)[C@@]([H])(CC[C@]3(OC(C)=O)C(C)=O)[C@]1([H])C=C(C)C4=CC(=O)CC[C@]24C
InChI	1S/C24H32O4/c1-14-12-18-19(22(4)9-6-17(27)13-21(14)22)7-10-23(5)20(18)8-11-24(23,15(2)25)28-16(3)26/h12-13,18-20H,6-11H2,1-5H3/t18-,19+,20+,22-,23+,24+/m1/s1
InChI key	RQZAXGRLVPAYTJ-GQFGMJRRSA-N
Gene Information	human ... PGR(5241)

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

pictograms	GHS08
signalword	Danger
hcodes	H360FD
pcodes	P201 - P202 - P280 - P308 + P313 - P405 - P501
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Mepenzolate bromide

Empirical Formula (Hill Notation):	C₂₁H₂₆BrNO₃
Linear Formula:	C₂₁H₂₆NO₃Br
CAS Number:	76-90-4
Molecular Weight:	420.34
EC Number:	200-992-7
MDL number:	MFCD00079450
PubChem Substance ID:	329818020
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	Br.C[N]1(C)CCCC(C1)OC(=O)C(O)(c2ccccc2)c3ccccc3
InChI	1S/C21H26NO3.BrH/c1-22(2)15-9-14-19(16-22)25-20(23)21(24,17-10-5-3-6-11-17)18-12-7-4-8-13-18;/h3-8,10-13,19,24H,9,14-16H2,1-2H3;1H
InChI key	FOPUTUUUOOOXQU-UHFFFAOYSA-N

Mepirizole belongs to the class of non-steroidal anti-inflammatory drugs (NSAIDs), widely used in the treatment of pain and inflammation.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
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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Mepirizole

Empirical Formula (Hill Notation):	C₁₁H₁₄N₄O₂
CAS Number:	18694-40-1
Molecular Weight:	234.25
EC Number:	242-507-1
MDL number:	MFCD00057351
PubChem Substance ID:	329818077

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

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
storage temp.	2-8°C
SMILES string	CC1=NC(N2C(OC)=CC(C)=N2)=NC(OC)=C1
InChI	1S/C11H14N4O2/c1-7-5-9(16-3)13-11(12-7)15-10(17-4)6-8(2)14-15/h5-6H,1-4H3
InChI key	RHAXSHUQNIEUEY-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
signalword	Warning
hcodes	H302 + H312 + H332 - H315 - H319 - H335
pcodes	P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, 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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Mersalyl acid

Empirical Formula (Hill Notation):	C₁₃H₁₇HgNO₆
Linear Formula:	HOHgCH₂CH(OCH₃)CH₂NHCOC₆H₄OCH₂CO₂H
CAS Number:	486-67-9
Molecular Weight:	483.87
EC Number:	207-637-5
MDL number:	MFCD00004302
PubChem Substance ID:	329818097
NACRES:	NA.24

1 g in glass bottle

Quality Level	100
grade	analytical standard
assay	85% (TLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	192-193 °C (dec.) (lit.)
solubility	NH₄OH: soluble, clear to hazy
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	COC(CNC(=O)c1ccccc1OCC(O)=O)C[Hg]O
InChI	1S/C13H16NO5.Hg.H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);;1H2/q;+1;/p-1
InChI key	HQRSUIDICNOLPX-UHFFFAOYSA-M

Mesitylene, a volatile organic compound (VOC), is a methyl substituted benzene hydrocarbon, widely utilized as a solvent for industrial and research applications.

pictograms	GHS06,GHS08,GHS09
signalword	Danger
hcodes	H300 + H310 + H330 - H373 - H410
pcodes	P262 - P273 - P280 - P301 + P310 + P330 - P302 + P352 + P310 - P304 + P340 + P310
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	UN 2025 6.1 / PGI
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Mesitylene

Empirical Formula (Hill Notation):	C₉H₁₂
Linear Formula:	C₆H₃(CH₃)₃
CAS Number:	108-67-8
Molecular Weight:	120.19
Beilstein/REAXYS Number:	906806
EC Number:	203-604-4
MDL number:	MFCD00008538
PubChem Substance ID:	329759906
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.
Mesitylene may be used as an analytical standard for the quantification of the analyte in human biological samples, environmental samples, organic solvent mixtures, and aerosolized jet fuels by gas chromatography (GC) based techniques.

Quality Level	100
grade	analytical standard
vapor density	4.1 (vs air)
vapor pressure	14 mmHg ( 55 °C), 2.49 mmHg ( 25 °C)
assay	99.8% (GC)
form	neat
autoignition temp.	1022 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	0.88-6.1 %, 100 °F
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.499 (lit.), n20/D 1.499
bp	163-166 °C (lit.)
mp	45 °C (lit.)
density	0.864 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	Cc1cc(C)cc(C)c1
InChI	1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3
InChI key	AUHZEENZYGFFBQ-UHFFFAOYSA-N