335975
(+)-1-(9-Fluorenyl)ethyl chloroformate solution
18 mM in acetone, derivatization grade (chiral)
Synonym(s):
(+)-FLEC solution
Sign In to View Organizational & Contract Pricing
Select a Size
About This Item
Empirical Formula (Hill Notation):
C16H13ClO2
CAS Number:
Molecular Weight:
272.73
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
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
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
General description
(+)-1-(9-Fluorenyl)ethyl chloroformate is a highly fluorescent compound1 commonly used as a chiral derivatizing agent for the separation of racemates prior to reversed-phase HPLC analysis.
Application
- Chiral analysis of β-methylamino alanine (BMAA) enantiomers: Details the use of (+)-1-(9-fluorenyl)-ethyl chloroformate (FLEC) for derivatization followed by LC-MS/MS analysis, improving the understanding of amino acids′ stereochemistry (Zurita et al., 2019).
- Enantioselective micellar electrokinetic chromatography of dl‐amino acids: Utilizes (+)-1-(9-fluorenyl)ethyl chloroformate derivatization combined with UV-induced fluorescence detection to analyze amino acids, enhancing analytical methodologies (Prior et al., 2018).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
Target Organs
Central nervous system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
1.4 °F
Flash Point(C)
-17 °C
Regulatory Information
危险化学品
易制毒化学品（3类）
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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
Radu-Cristian Moldovan et al.
Journal of chromatography. A, 1564, 199-206 (2018-06-19)
A targeted CE-MS approach was developed for the chiral analysis of biologically relevant amino acids in artificial cerebrospinal fluid (aCSF). In order to achieve chiral resolution, the five amino acids (Ser, Asn, Asp, Gln and Glu) were derivatized with (+)-1-(9-fluorenyl)ethyl
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service