Fluorescamine
Structural Formula Vector Image
Title: Fluorescamine
CAS Registry Number: 38183-12-9
CAS Name: 4-Phenylspiro[furan-2(3H),1¢(3¢H)-isobenzofuran]-3,3¢-dione
Additional Names: 4-phenylspiro[furan-2(3H),1¢-phthalan]-3,3¢-dione
Manufacturers' Codes: Ro-20-7234
Trademarks: Fluram (Roche)
Molecular Formula: C17H10O4
Molecular Weight: 278.26
Percent Composition: C 73.38%, H 3.62%, O 23.00%
Literature References: Non-fluorescent reagent that reacts readily with primary amines to form highly fluorescent compds: S. Udenfriend et al., Science 178, 871 (1972). Prepn: M. Weigele et al., J. Am. Chem. Soc. 94, 5927 (1972); eidem, J. Org. Chem. 41, 388 (1976). Use as fluorometric reagent: W. Leimgruber, M. Weigele, DE 2350179; eidem, US 3830629 (both 1974 to Hoffmann-La Roche). Review of analytical uses: C. Y. Lai, Methods Enzymol. 47, 236-243 (1977); S. Stein, Peptides in Neurobiology, H. Gainer, Ed. (Plenum, New York, 1977) pp 9-37; S. Udenfriend, Pharmacology 19, 223-227 (1979).
Properties: mp 154-155°. uv max (ether): 235, 276, 284, 306 nm (e 25900, 3950, 4100, 3800).
Melting point: mp 154-155°
Absorption maximum: uv max (ether): 235, 276, 284, 306 nm (e 25900, 3950, 4100, 3800)
Use: Analytical reagent.

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