BIOshell™ A160 Peptide C18, 2.7 m HPLC Column 66905-U

NACRES:

SB.52

BIOshell™ 160 Peptide C18 columns are specifically engineered to provide efficient separation of peptides as well as small proteins. These columns contain advanced Fused-Core particles with pores strategically sized to 160 to enable optimized peptide diffusion. This attribute makes these columns an excellent choice for peptide mapping. Additionally, the sterically-protected C18 ligands provide extra stability allowing the columns to be used at an extended pH range (2-9) and high temperatures (up to 90 °C). This greatly expands the application range for the separation of biomolecules.
UHPLC Analysis of Peptides on BIOshell™ A160 Peptide C18, CN, and Phenyl-Hexyl, 2.7 µm
BIOshell™ A160 Peptide C18, 2.7 µm HPLC Column, a non-end capped column that has superficially porous particle with C18 alkyl ligand as the stationary phase, is used mainly in the separation of peptides at a good flow rate.
BIOshell™ A160 Peptide C18, 2.7 µm HPLC Columns are compatible both with UHPLC and HPLC systems. They are specifically engineered for the fast and high-resolution seperation of biomolecules. These columns operate at high flow rates and have 40% higher efficiency than columns with fully porous particles of the same size. They are stable at high temperatures, which increases the throughput and enhances the peak shape.
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BIOshell is a trademark of Sigma-Aldrich Co. LLC

Quality Level	100
material	stainless steel hardware
Agency/Method	suitable for USP L1
description	Shell thickness (0.5 µm), Solid Core (1.7 µm)
feature	endcapped: no
analyte chemical class(es)	peptides
Торговая марка	BIOshell™
extent of labeling	4.6% carbon loading
parameter	600 bar max. pressure, 90 °C max. temp.
application(s)	HPLC: suitable, UHPLC: suitable
L x I.D.	15 cm x 2.1 mm
surface coverage	2.2 µmol/m2
matrix	spherical silica particle platform
matrix active group	C18 (octadecyl) bonding phase, diisobutyloctadecyl
particle size	2.7 µm
pore size	160 A
surface area	90 m2/g
operating pH range	1 - 8
separation technique	reversed phase