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Merck
CN

23182

Supelco

氯甲酸(+)-1-(9-芴)乙酯 溶液

≥18 mM in acetone, for chiral derivatization, LiChropur

别名:

(+)-FLEC 溶液

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About This Item

经验公式(希尔记法):
C16H13ClO2
分子量:
272.73
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.22

等级

for chiral derivatization

质量水平

产品线

ChiraSelect

光学纯度

enantiomeric ratio: ≥99.0:1.0 (HPLC)

质量

LiChropur

浓度

≥18 mM in acetone

技术

HPLC: suitable

折射率

n20/D 1.359

储存温度

2-8°C

InChI

1S/C16H13ClO2/c1-10(19-16(17)18)15-13-8-4-2-6-11(13)12-7-3-5-9-14(12)15/h2-10,15H,1H3

InChI key

SFRVOKMRHPQYGE-UHFFFAOYSA-N

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一般描述

(+)-1-(9-芴基)氯甲酸乙酯 [(+)-FLEC] 是一种手性衍生试剂。有助于分离 α 的对映体-氨基酸,以及有助于采用 HPLC 法测定其光学纯度。

应用

(+)-FLEC 可用于反相高效液相色谱-荧光检测系统的草铵膦对映选择性分析。

外形

溶液,5mg 溶于 1mL 丙酮中

其他说明

伯、仲氨基酸和胺的手性衍生化试剂。通过反相液相色谱分离衍生物,荧光检测对映体的纯度

推荐产品

发现适用于高效液相色谱液相色谱-质谱分析的理想 LiChropur 试剂

法律信息

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

FlameExclamation mark

警示用语:

Danger

危险声明

危险分类

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

靶器官

Central nervous system

补充剂危害

WGK

WGK 2

闪点(°F)

1.4 °F

闪点(°C)

-17 °C

法规信息

易制毒化学品(3类)
危险化学品

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Separation of enantiomers of a-hydroxy acids by reversed-phase liquid chromatography after derivatization with 1-(9-fluorenyl) ethyl chloroformate.
Fransson, Bengt, and Ulf Ragnarsson.
Journal of Chromatography A, 827, 31-36 (1998)
Zeineb Aturki et al.
Electrophoresis, 25(4-5), 607-614 (2004-02-26)
The indirect resolution of five beta-adrenoreceptor blocking agents (propranolol, oxprenolol, pindolol, metoprolol, and atenolol) using precolumn derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate (FLEC), and capillary electrochromatography (CEC) is reported. Three octadecylsilanized (ODS) silica gel-based stationary phases, differing in particle diameter and carbon
A Roux et al.
Journal of chromatography, 570(2), 453-461 (1991-10-04)
A method for the determination of the R-(+) and S-(-) enantiomers of propranolol in blood was developed. After extraction with heptane-isopentanol and derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate, excess reagent was removed using solid-phase extraction. The enantiomers were separated on an achiral
Michelle A Camerino et al.
Organic & biomolecular chemistry, 11(16), 2571-2573 (2013-03-14)
An efficient synthesis of the enantiomers of fluorenylethylchloroformate (FLEC) has been achieved that allows the routine application of the reagent for the resolution of chiral amines including unusual amino acids. The utility of the fluorenylethoxycarbonyl (Feoc) group as a chiral
[A method for separation of DL-amino acids].
T H Akiyama et al.
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 40(1), 76-83 (1995-01-01)

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