Arsphenamine
Title: Arsphenamine
CAS Registry Number: 139-93-5
Additional Names: salvarsan
Manufacturers' Codes: Ehrlich 606
Literature References: Originally introduced as an antisyphilitic. Initially characterized as 4,4ยข-(1,2-diarsenediyl)bis[2-aminophenol] dihydrochloride; composition was later determined to be of a mixture of cyclic 3-amino-4-hydroxyphenylarsenic species. Prepn: P. Ehrlich, A. Bertheim, US 986148 (1911 to Hoechst); eidem, Ber. 45, 756 (1912); W. A. Christiansen, J. Am. Chem. Soc. 42, 2402 (1920). Toxicity data: J. F. Schamberg et al., Am. J. Syph. Neurol. 18, 37 (1934). Review of structure: A. S. Levinson, J. Chem. Educ. 54, 98-99 (1977). MS determn of chemical composition: N. C. Lloyd et al., Angew. Chem. Int. Ed. 44, 941 (2005).
Properties: Light yellow, somewhat hygroscopic powder. It is odorless, or has a slight odor of the precipitant used. Oxidizes on exposure to air, becoming darker and more toxic. It is poisonous! Sol in water, alc or glycerol, very slightly sol in chloroform or ether. Its aq soln is acid; pH about 3. LD100 i.v. in rats: 140 mg/kg (Schamberg).
Toxicity data: LD100 i.v. in rats: 140 mg/kg (Schamberg)

Others monographs:
p-DimethylaminoazobenzeneFrangulinPropyl PropionateAnthramycin
Ethyl CaprylateAcetophenazinePotassium Oleate6-Methoxy-α-tetralone
MesteroloneSatumomabTryparsamideTetraphenylarsonium Bromide
Metolazone3-(o-Methoxyphenyl)-2-phenylacrylic AcidPyromellitic Acidtert-Butyl Bromide
©2016 DrugLead US FDA&EMEA