Chlornaphazine
Structural Formula Vector Image
Title: Chlornaphazine
CAS Registry Number: 494-03-1
CAS Name: N,N-Bis(2-chloroethyl)-2-naphthylamine
Additional Names: dichloroethyl-b-naphthylamine; b-naphthyldi(2-chloroethyl)amine; b-naphthylbis(b-chloroethyl)amine; di(2-chloroethyl)-b-naphthylamine
Manufacturers' Codes: CB-1048; R-48
Trademarks: Cloronaftina; Erysan
Molecular Formula: C14H15Cl2N
Molecular Weight: 268.18
Percent Composition: C 62.70%, H 5.64%, Cl 26.44%, N 5.22%
Literature References: Prepd from 2-C10H7N(C2H4OH)2 by treatment with POCl3: Ross, J. Chem. Soc. 1949, 183; Ghielmetti, Farmaco Ed. Sci. 5, 275 (1950); 11, 603 (1956). Mechanism of action studies: Jeney et al., Kiserl. Orvostud. 20, 369 (1968), C.A. 70, 18766j (1969). Review of carcinogenicity studies: IARC Monographs 4, 119-124 (1974).
Properties: Platelets from petr ether, mp 54-56°. bp5 210°. Very sparingly sol in water, glycerol. More sol (in ascending degree) in petr ether, ethanol, olive oil, ether, acetone, benzene.
Melting point: mp 54-56°
Boiling point: bp5 210°
CAUTION: This substance has been listed as a known carcinogen: Fourth Annual Report on Carcinogens (NTP 85-002, 1985) p 44; delisted because no U.S. residents exposed: Fifth Annual Report on Carcinogens (NTP 89-239, 1989) p 340.
Therap-Cat: Antineoplastic.
Keywords: Antineoplastic; Alkylating Agents; Nitrogen Mustards.

Other Monographs:
N4-SulfanilylsulfanilamideLysine AcetylsalicylateCornusSphingosine
ViloxazineCalcium Ferrous CitrateCrotoxyphosCholestyramine Resin
Boron MonoxideBetoxycaineNeopterinIsothebaine
Ethyl ChloroacetateFenoxanilFerrous SelenideAvermectins
©2006-2023 DrugFuture->Chemical Index Database