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9-Fluorenylmethyl Chloroformate

<strong> 9-Fluorenylmethyl Chloroformate</strong>_x000D_ <strong>Catalog number:</strong> B2014740_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 258.70_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8 ¬∞C_x000D_ <strong>Keywords:</strong> Fmoc-Cl, Chloroformic Acid 9-Fluorenylmethyl Ester, (9H-Fluoren-9-ylmethoxy)carbonyl Chloride_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MŒ©-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Herr√°ez-Hern√°ndez R, Camp√≠ns-Falc√≥ P. Derivatization of tertiary amphetamines with 9-fluorenylmethyl chloroformate for liquid chromatography: determination of N-methylephedrine Analyst. 2000 Jun;125(6):1071-6._x000D_ 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._x000D_ 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._x000D_ 4: Zhou Y, Lin Q, Jin C, Cheng L, Zheng X, Dai M, Zhang Y. Simultaneous analysis of N(Œµ) -(carboxymethyl)Lysine and N(Œµ) -(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._x000D_ 5: Siciliano C, De Marco R, Guidi LE, Spinella M, Liguori A. A one-pot procedure for the preparation of N-9-fluorenylmethyloxycarbonyl-Œ±-amino diazoketones from ��±-amino acids J Org Chem. 2012 Dec 7;77(23):10575-82._x000D_ 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._x000D_ 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._x000D_ 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._x000D_ 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._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/10027269">10: Wilkins MR, Yan JX, Gooley AA. 2-DE spot amino acid analysis with 9-fluorenylmethyl chloroformate Methods Mol Biol. 1999;112:445-60. </a>_x000D_ _x000D_ <strong>Products Related to 9-Fluorenylmethyl Chloroformate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>

Product Specifications

Short Description

Catalog Number: B2014740 (1 g)

Weight

0.8

Length

2

Width

0.9

Height

0.9

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