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75033AST

Supelco

Astec® CHIRALDEX G-BP Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

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eCl@ss:
32110502
NACRES:
SB.54

material

fused silica

Quality Level

description

GC capillary column

parameter

-10-200 °C temperature (isothermal)
-10-220 °C temperature (programmed)

Beta value

500

df

0.12 μm

technique(s)

gas chromatography (GC): suitable

L × I.D.

30 m × 0.25 mm

matrix active group

non-bonded; 2,6-di-O-pentyl-3-butyryl derivative of γ-cyclodextrin phase

application(s)

agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)

column type

capillary chiral

separation technique

chiral

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This Item
73003AST74033AST73023AST
matrix active group

non-bonded; 2,6-di-O-pentyl-3-butyryl derivative of γ-cyclodextrin phase

matrix active group

non-bonded; 2,6-di-O-pentyl-3-trifluoroacetyl derivative of α-cyclodextrin phase

matrix active group

non-bonded; 2,6-di-O-pentyl-3-propionyl derivative of γ-cyclodextrin phase

matrix active group

non-bonded; 2,6-di-O-pentyl-3-trifluoroacetyl derivative of β-cyclodextrin phase

parameter

-10-200 °C temperature (isothermal), -10-220 °C temperature (programmed)

parameter

-10-180 °C temperature (isothermal or programmed)

parameter

-10-200 °C temperature (isothermal), -10-220 °C temperature (programmed)

parameter

-10-180 °C temperature (isothermal or programmed)

column type

capillary chiral

column type

capillary chiral

column type

capillary chiral

column type

capillary chiral

technique(s)

gas chromatography (GC): suitable

technique(s)

gas chromatography (GC): suitable

technique(s)

gas chromatography (GC): suitable

technique(s)

gas chromatography (GC): suitable

application(s)

agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)

application(s)

agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)

application(s)

agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)

application(s)

agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)

General description

Incorporates a phase consisting of a 2,6-di-O-pentyl-3-butyryl derivative of γ-cyclodextrin. This phase exhibits high selectivity for amino acids, amines, and furans.

Chem/Phys Resistance

Temp. Limits:
  • -10 °C to 200 °C isothermal, 220 °C programmed

Other Notes

We offer a variety of chromatography accessories including analytical syringes

Legal Information

Astec is a registered trademark of Merck KGaA, Darmstadt, Germany
CHIRALDEX is a trademark of Sigma-Aldrich Co. LLC

Certificates of Analysis (COA)

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Jared L Anderson et al.
Journal of chromatography. A, 946(1-2), 197-208 (2002-03-05)
The separation of 17 chiral sulfoxides and eight chiral sulfinate esters by gas chromatography (GC) on four derivatized cyclodextrin chiral stationary phases (CSPs) (Chiraldex G-TA, G-BP, G-PN, B-DM) is presented. Many of these compounds are structural isomers or part of
Ke Huang et al.
Tetrahedron, asymmetry, 17(19), 2821-2832 (2006-10-27)
The enantiomeric excess of chiral reagents used in asymmetric syntheses directly affects the reaction selectivity and product purity. In this work, 84 of the more recently available chiral compounds were evaluated to determine their actual enantiomeric composition. These compounds are
Enantiomeric impurities in chiral catalysts, auxiliaries, and synthons used in enantioselective syntheses. Part 4
Qui, Haiziao, et al.
Tetrahedron Asymmetry, 24 (18), 1134-1141 (2013)

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