335975
氯甲酸(+)-1-(9-芴)乙酯 溶液
18 mM in acetone, derivatization grade (chiral)
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
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Form:
liquid
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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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。
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）。
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)
Separation of amino acid enantiomers and chiral amines using precolumn derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate and reversed-phase liquid chromatography.
S Einarsson et al.
Analytical chemistry, 59(8), 1191-1195 (1987-04-15)
Yasushi Hori et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 776(2), 191-198 (2002-07-26)
We have developed a new analytical method to quantify the DL-homoalanine-4-yl(methyl)phosphinate (DL-GLUF) enantiomers in biological specimens using a reversed-phase high-performance liquid chromatography system with a fluorescence detection system. The derivatization of DL-GLUF enantiomers with (+)-1-(9-fluorenyl)ethyl chloroformate was carried out under
E Frigerio et al.
Journal of chromatography. A, 660(1-2), 351-358 (1994-02-04)
A sensitive and selective high-performance liquid chromatographic method for the determination of reboxetine enantiomers in human plasma was developed. Although two chiral centres are present in reboxetine, its stereospecific synthesis leads to two rather than four possible enantiomers. After extraction
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
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