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77023AST

Supelco

Astec® CHIRALDEX B-DM Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

동의어(들):

GC column, chiral, beta-dextran

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About This Item

UNSPSC 코드:
41115710
NACRES:
SB.54

material

fused silica

Quality Level

설명

GC capillary column

포장

pkg of 1 ea

파라미터

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

베타 값

500

df

0.12 μm

기술

gas chromatography (GC): suitable

길이 × I.D.

30 m × 0.25 mm

기질 활성군

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

응용 분야

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)

컬럼 유형

capillary chiral

분리 기술

chiral

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Through special derivatization techniques, the concentration of the cyclodextrin in the CHIRALDEX B-DM has been substantially increased in the polysiloxane carrier. This phase is very useful for a number of free acids and bases. The B-DM is able to perform most of the separations done on a beta-permethylated phase, but with higher resolution. The selectivity of the B-DM covers applications of both the B-PM and B-PH phases, although with superior performance.

애플리케이션

It has been used for enantiomeric separation of ephedrine, pseudoephedrine, chlorinated intermediates and methylamphetamine using gas chromatographic analysis.

화학적/생리학적 저항성

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

기타 정보

We offer a variety of chromatography accessories including analytical syringes

법적 정보

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

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Chiral gas chromatography as a tool for investigations into illicitly manufactured methylamphetamine.
Morrison, Calum, et al.
Chirality, 23.7, 519-519 (2011)
Evaluating dynamic kinetic resolution strategies in the asymmetric hydrosilylation of cyclic ketimines
Jones, Simon; Zhao, Peichao
Tetrahedron, 25 (3), 238-244 (2014)
Rh-catalyzed asymmetric hydrogenation using a furanoside monophosphite second-generation ligand library: scope and limitations
Alegre, Sabina, et al.
Tetrahedron, 25 (3), 258-262 (2014)
Synthesis of a chiral asymmetrical NCN ligand and its metallation
Sylla Dieng, Pape,et al.
Comptes Rendus Chimie, 12 (5), 560-564 (2009)
J Mydlová et al.
Journal of chromatography. A, 1150(1-2), 124-130 (2007-03-24)
The enantiomers of dialkyl 2,3-pentadienedioate undergo interconversion during gas chromatographic separation on chiral stationary phases. In this paper the on-column apparent interconversion kinetic and thermodynamic activation data were determined for dimethyl, diethyl, propylbutyl and dibutyl 2,3-pentadienedioate enantiomers by gas chromatographic

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