Picloxydine
Structural Formula Vector Image
Title: Picloxydine
CAS Registry Number: 5636-92-0
CAS Name: N,N¢¢-Bis[[(4-chlorophenyl)amino]iminomethyl]-1,4-piperazine dicarboximidamide
Additional Names: N,N¢¢-bis[(p-chlorophenyl)amidino]-1,4-piperazinedicarboxamidine; 1,4-bis(N4¢-p-chlorophenylamidinoamidinyl)piperazine; 1,1¢-[1,4-piperazinediylbis(imidocarbonyl)]bis[3-(p-chlorophenyl)guanidine]
Molecular Formula: C20H24Cl2N10
Molecular Weight: 475.38
Percent Composition: C 50.53%, H 5.09%, Cl 14.92%, N 29.46%
Literature References: Heterocyclic biguanide with antibacterial activity. Prepn: J. W. James, L. F. Wiggins, GB 855017; eidem, US 3101336 (1960, 1963 both to Aspro-Nicholas). Prepn and antibacterial spectrum: J. W. James et al., J. Med. Chem. 11, 942 (1968). Bactericidal effect in disinfectant formulations: A. M. Gordon, J. Clin. Pathol. 22, 496 (1969). Mode of action study: B. D. Rawal, J. V. Hardy, Microbios 14, 135 (1974). In vitro activity vs Chlamydia trachomatis: D. Thomas et al., Pathol. Biol. 32, 544 (1984).
 
Derivative Type: Dihydrochloride
CAS Registry Number: 19803-62-4
Trademarks: Vitabact (Faure)
Molecular Formula: C20H24Cl2N10.2HCl
Molecular Weight: 548.30
Percent Composition: C 43.81%, H 4.78%, Cl 25.86%, N 25.55%
Properties: Crystals from water, mp 274°. LD50 in mice (mg/kg): 150 i.p. (James).
Melting point: mp 274°
Toxicity data: LD50 in mice (mg/kg): 150 i.p. (James)
 
Therap-Cat: Antibacterial (topical).
Keywords: Antiseptic/Disinfectant; Guanidines.

Other Monographs:
Sodium BisulfiteBethanidineAluminonTristearin
4,4'-DifluorodiphenylPentoxylVincamineMecloralurea
RizatriptanThifensulfuron-methylLimestonePhenylselenotrimethylsilane
TrichlormethiazideJojoba Oil2-MethylanthraquinoneFibrolase
©2006-2023 DrugFuture->Chemical Index Database