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9-Fluorenylmethyl Chloroformate

Original price was: $1,395.00.Current price is: $695.00.

Catalog Number: B2014740 (1 g)
9-Fluorenylmethyl Chloroformate is a high quality 9-Fluorenylmethyl Chloroformate, an N-Protecting Agent for Peptides. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (2 votes)

9-Fluorenylmethyl Chloroformate
Catalog number: B2014740
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 258.70
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: 2-8 °C
Keywords: Fmoc-Cl, Chloroformic Acid 9-Fluorenylmethyl Ester, (9H-Fluoren-9-ylmethoxy)carbonyl Chloride
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Herráez-Hernández R, Campíns-Falcó P. Derivatization of tertiary amphetamines with 9-fluorenylmethyl chloroformate for liquid chromatography: determination of N-methylephedrine Analyst. 2000 Jun;125(6):1071-6.
2: Mohammadi B, Majnooni MB, Khatabi PM, Jalili R, Bahrami G. 9-fluorenylmethyl chloroformate as a fluorescence-labeling reagent for derivatization of carboxylic acid moiety of sodium valproate using liquid chromatography/tandem mass spectrometry for binding characterization: a human pharmacokinetic study J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Jan 1;880(1):12-8.
3: Nakano M, Higo D, Arai E, Nakagawa T, Kakehi K, Taniguchi N, Kondo A. Capillary electrophoresis-electrospray ionization mass spectrometry for rapid and sensitive N-glycan analysis of glycoproteins as 9-fluorenylmethyl derivatives Glycobiology. 2009 Feb;19(2):135-43.
4: Zhou Y, Lin Q, Jin C, Cheng L, Zheng X, Dai M, Zhang Y. Simultaneous analysis of N(ε) -(carboxymethyl)Lysine and N(ε) -(carboxyethyl)lysine in foods by ultra-performance liquid chromatography-mass spectrometry with derivatization by 9-fluorenylmethyl chloroformate J Food Sci. 2015 Feb;80(2):C207-17.
5: Siciliano C, De Marco R, Guidi LE, Spinella M, Liguori A. A one-pot procedure for the preparation of N-9-fluorenylmethyloxycarbonyl-α-amino diazoketones from α-amino acids J Org Chem. 2012 Dec 7;77(23):10575-82.
6: Chen Y, Chen Q, Tang S, Xiao X. LC method for the analysis of kanamycin residue in swine tissues using derivatization with 9-fluorenylmethyl chloroformate J Sep Sci. 2009 Nov;32(21):3620-6.
7: Kinoshita M, Saito A, Yamamoto S, Suzuki S. A practical method for preparing fluorescent-labeled glycans with a 9-fluorenylmethyl derivative to simplify a fluorimetric HPLC-based analysis J Pharm Biomed Anal. 2020 Jul 15;186:113267.
8: Huang TM, Deng CH, Chen NZ, Liu Z, Duan GL. High performance liquid chromatography for the determination of glucosamine sulfate in human plasma after derivatization with 9-fluorenylmethyl chloroformate J Sep Sci. 2006 Oct;29(15):2296-302.
9: Gu Z, Lei W, Shi W, Hao Q, Si W, Xia X, Wang F. Studies on the interaction between 9-fluorenylmethyl chloroformate and Fe3+ and Cu2+ ions: spectroscopic and theoretical calculation approach Spectrochim Acta A Mol Biomol Spectrosc. 2014 Nov 11;132:361-8.
10: Wilkins MR, Yan JX, Gooley AA. 2-DE spot amino acid analysis with 9-fluorenylmethyl chloroformate Methods Mol Biol. 1999;112:445-60.

Products Related to 9-Fluorenylmethyl Chloroformate can be found at Chemicals

Additional Information

Weight 0.8 oz
Dimensions 2 × 0.9 × 0.9 in
5/5 - (2 votes)

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