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Merck
CN

23182

Supelco

氯甲酸(+)-1-(9-芴)乙酯 溶液

≥18 mM in acetone, derivatization grade (chiral), LiChropur

别名:

(+)-FLEC 溶液

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关于此项目

经验公式(希尔记法):
C16H13ClO2
CAS Number:
分子量:
272.73
MDL编号:
UNSPSC代码:
41115716
PubChem化学物质编号:
NACRES:
NA.22
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等级

derivatization grade (chiral)

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

SMILES字符串

ClC(=O)OC(C1c2c(cccc2)c3c1cccc3)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
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

储存分类代码

3 - Flammable liquids

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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 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)
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
Sascha Freimüller et al.
Journal of pharmaceutical and biomedical analysis, 30(2), 209-218 (2002-08-23)
An indirect enantioseparation method for robust and precise determination of D-Carnitine (D-C) in L-Carnitine (L-C) in the range of 0.1-1.0% is presented. The method is based on derivatization of Carnitine with (+)-[1-(9-fluorenyl)-ethyl]-chloroformate ((+)-FLEC). The two diastereomers are subsequently separated of

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