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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
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Form:
liquid
产品名称
氯甲酸(+)-1-(9-芴)乙酯 溶液, 18 mM in acetone, derivatization grade (chiral)
SMILES string
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
grade
derivatization grade (chiral)
vapor density
2 (vs air)
vapor pressure
180 mmHg ( 20 °C)
form
liquid
concentration
18 mM in acetone
refractive index
n20/D 1.3602
density
0.79 g/mL at 25 °C
functional group
chloro
storage temp.
2-8°C
Quality Level
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Application
- β-甲基氨基丙氨酸(BMAA)对映体的手性分析:详细介绍了氯甲酸(+)-1--9-芴基乙酯(FLEC)的衍生化和随后的LC-MS/MS分析,增进了我们对氨基酸′立体化学的理解 (Zurita et al., 2019)。
- DL-氨基酸的对映选择性胶束电动色谱:利用氯甲酸(+)-1--9-芴基乙酯进行衍生化,结合UV诱导的荧光检测进行氨基酸的分析,改善了分析方法(Prior et al., 2018)。
General description
(+)-1-(9-芴基)乙基氯甲酸酯是高度荧光的化合物 1,通常用作手性衍生剂,用在进行反相 HPLC 分析之前分离外消旋体。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
1.4 °F
flash_point_c
-17 °C
法规信息
危险化学品
易制毒化学品(3类)
此项目有
Reversed-phase high-performance liquid chromatographic analysis of atenolol enantiomers in plasma after chiral derivatization with (+)-1-(9-fluorenyl) ethyl chloroformate.
Rosseel MT, et al.
Journal of Chromatography. B, Biomedical Applications, 568(1), 239-245 (1991)
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
Radu-Cristian Moldovan et al.
Journal of chromatography. A, 1513, 1-17 (2017-08-02)
Over the last 30years, (±)-1-(9-fluorenyl)ethyl chloroformate ((±)-FLEC) was used as a chiral derivatizing agent in various analytical applications involving a wide range of endogenous, pharmaceutical and environmentally relevant molecules. This comprehensive review aims to present all the significant aspects related
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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