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Merck
CN

23182

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
化学文摘社编号:
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
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
N Todoroki et al.
Journal of chromatography. B, Biomedical sciences and applications, 728(1), 41-47 (1999-06-24)
The natural occurrence of N-methyl-D-aspartate (NMDA) is limited to the foot muscle of Scapharca broughtonii; it is a well known compound for its neuroexitatory activity. This paper describes a high-performance liquid chromatographic (HPLC) method for the determination of NMDA in
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
F Lai et al.
Journal of pharmaceutical and biomedical analysis, 11(2), 117-120 (1993-02-01)
In the liquid chromatographic analysis of pharmaceuticals, two challenges are often encountered: detectivity and chiral separations. Propranolol, a beta adrenergic blocker, is a pharmaceutical compound that faces both of these limitations. In this study, both limitations are overcome simultaneously using
T Teerlink et al.
Clinica chimica acta; international journal of clinical chemistry, 183(3), 309-315 (1989-08-31)
A method to measure total hydroxyproline in human urine was developed. Primary amino acids were derivatized with ortho-phthaldialdehyde, followed by derivatization of imino acids with 9-fluorenylmethyl chloroformate. The fluorescent 9-fluorenylmethyl chloroformate derivatives were separated by reversed phase high-performance liquid chromatography.

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