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71023AST

Supelco

Astec® CHIRALDEX™ B-PH Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

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1 EA
CZK 50,500.00

CZK 50,500.00

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1 EA
CZK 50,500.00

About This Item

UNSPSC Code:
41115710
NACRES:
SB.54

CZK 50,500.00

Please contact Customer Service for Availability

material

fused silica

Quality Level

100

description

GC capillary column

packaging

pkg of 1 ea

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; (S)-2-hydroxy propyl methyl ether derivative of β-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

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Astec® CHIRALDEX™ B-PH Capillary GC Column L × I.D. 30 m × 0.25 mm, df 0.12 μm

71023AST

Astec® CHIRALDEX™ B-PH Capillary GC Column

Astec® CHIRALDEX™ B-PM Capillary GC Column L × I.D. 30 m × 0.25 mm, df 0.12 μm

76023AST

Astec® CHIRALDEX™ B-PM Capillary GC Column

Astec® CHIRALDEX™ G-DP Capillary GC Column L × I.D. 30 m × 0.25 mm, df 0.12 μm

78033AST

Astec® CHIRALDEX™ G-DP Capillary GC Column

Astec® CHIRALDEX™ B-DP Capillary GC Column L × I.D. 30 m × 0.25 mm, df 0.12 μm

78023AST

Astec® CHIRALDEX™ B-DP Capillary GC Column

matrix active group

non-bonded; (S)-2-hydroxy propyl methyl ether derivative of β-cyclodextrin phase

matrix active group

non-bonded; 2,3,6-tri-O-methyl derivative of β-cyclodextrin phase

matrix active group

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

matrix active group

non-bonded; 2,3-di-O-propionyl-6-t-butyl silyl derivative of β-cyclodextrin phase

df

0.12 μm

df

0.12 μm

df

0.12 μm

df

0.12 μm

parameter

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

parameter

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

parameter

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

parameter

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

material

fused silica

material

fused silica

material

fused silica

material

fused silica

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

CHIRALDEX B-PH shows at least some selectivity to a great variety of analytes, but is especially effective for saturated analytes with minimal functionality, saturated cyclics and bicyclics. The CHIRALDEX PH series of columns shows less of a necessity for inclusion complexation for chiral recognition than the DA columns. This phase often shows a reversal of elution order (enantioreversal) compared to the B-DA phase.

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

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Certificates of Analysis (COA)

Lot/Batch Number
287225-04
287225-03
287225-02
287225-01
286726-04

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Enantioselective conjugate addition with chiral amidocuprates, part III. Studies on the synthetic optimization of MAPP-cuprates.
Rossiter, Bryant E., et al.
Tetrahedron Asymmetry, 3 (2), 231-234 (1992)
Alkali metal fluorides as efficient fluorinating agents. Enantiocontroued synthesis of 2-fluoroalkyl carboxylates and 1-fluoroalkyl benzenes
Fritz-Langhals, Eike
Tetrahedron Asymmetry, 5 (6), 981-986 (1994)
Asymmetric reductions in aqueous media: enzymatic synthesis in cyclodextrin containing buffers
Zelinski, Thomas, et al.
Tetrahedron Asymmetry, 10 (9), 1681-1687 (1999)

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