추천 제품
material
fused silica
설명
GC capillary column
포장
1 ea of
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; 2,6-di-O-pentyl-3-propionyl derivative of γ-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
Incorporates a phase consisting of a 2,6-di-O-pentyl-3-propionyl derivative of γ-cyclodextrin. This phase exhibits high selectivity for lactones and aromatic amines. It is also suitable for epoxide separations. Additionally, the analysis of styrene oxide can be accomplished on this phase (this analyte degrades on the TA phases).
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
애플리케이션
제품 번호
설명
가격
Use of esterified and unesterified dipentylated y-, ?- and a-cyclodextrins as gas chromatographic stationary phases to indicate the structure of monoterpenoid constituents of volatile oils
Journal of Chromatography A, 672 (1-2), 254-260 (1994)
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The enantiomeric ratio of methylamphetamine (MAMP) is closely related to the optical activity of precursors and reagents used for the synthesis and this knowledge can provide useful information concerning the origins and synthetic methods used for illicit manufacture. The information
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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
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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
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