추천 제품
product name
Astec® CHIROBIOTIC® HPLC Column Screening Kit, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
material
stainless steel column
Quality Level
제품 라인
Astec®
포장
pkg of 1 kit
제조업체/상표
Astec®
파라미터
0-45 °C temperature
241 bar pressure (3500 psi)
기술
HPLC: suitable
LC/MS: suitable
길이 × I.D.
10 cm × 4.6 mm
기질
fully porous particle
입자 크기
5 μm
공극 크기
100 Å pore size
작동 pH
3.5-6.8
분리 기술
chiral
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관련 카테고리
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제품 번호
설명
SDS
- 15022ASTAstec® CHIROBIOTIC® V2 Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mmSDS
- 12022ASTAstec® CHIROBIOTIC® T Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mmSDS
- 13022ASTAstec® CHIROBIOTIC® R Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mmSDS
- 14022ASTAstec® CHIROBIOTIC® TAG Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mmSDS
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시험 성적서(COA)
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If you need assistance, please contact 고객 지원 부서
Chromatography Liquid Chiral Separations
Encyclopedia of Separation Science, 1-15 (2000)
Chromatographic Separations and Analysis: Macrocyclic Glycopeptide Chiral Stationary Phases
Comprehensive Chirality, 8, 227-262 (2012)
Journal of chromatography. A, 978(1-2), 185-204 (2002-12-03)
The chiral recognition capabilities of three macrocyclic glycopeptide chiral selectors, namely teicoplanin (Chirobiotic T), its aglycone (Chirobiotic TAG) and ristocetin (Chirobiotic R), were evaluated with supercritical and subcritical fluid mobile phases. A set of 111 chiral compounds including heterocycles, analgesics
Journal of chromatography. A, 1241, 60-68 (2012-05-04)
A chiral HPLC method using four macrocyclic antibiotic chiral stationary phases (CSPs) has been investigated for determination of the enantiomeric purity of fourteen new chiral derivatives of xanthones (CDXs). The separations were performed with the CSPs Chirobiotic T, Chirobiotic TAG
High-performance liquid chromatographic enantioseparation of bicalutamide and its related compounds.
Journal of chromatography. A, 1098(1-2), 75-81 (2005-11-30)
Direct high-performance liquid chromatographic methods were developed for the enantioseparation of (R,S)-bicalutamide (1) and its analogs (+/-)-3-chloro-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide (2), (+/-)-N-(4-cyano-3-(trifluoro-methyl)phenyl)-2-methyloxirane-2-carboxamide (3), (+/-)-4-fluorophenylsulfonyl-2-hydroxy-2-methylpropionic acid (4) and (+/-)-3-hydroxy-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide (5). The methods involved the use of a cellulose-based Chiralcel OD-H, macrocyclic glycopeptide-based Chirobiotic T
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