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Basic Information
CAS No.: 53-46-3
Name: METHANTHELINE BROMIDE (200 MG)
Molecular Structure:
Molecular Structure of 53-46-3 (METHANTHELINE BROMIDE (200 MG))
Formula: C21H26 N O3 . Br
Molecular Weight: 420.346
Synonyms: Ammonium,diethyl(2-hydroxyethyl)methyl-, bromide, xanthene-9-carboxylate (8CI);Diethyl(2-hydroxyethyl)methylammonium bromide, xanthene-9-carboxylate (7CI);Ethanaminium, N,N-diethyl-N-methyl-2-[(9H-xanthen-9-ylcarbonyl)oxy]-, bromide(9CI); Asabaine; Avagal; Banthin; Banthine; Banthine bromide; Doladene;Frenogastrico; Gastron; Gastrosedan; MTB 51; Mantheline; Metantyl; Metanyl;Metaxan; Methanide; Methantheline bromide; Methanthelinium bromide; Methanthinebromide; Methelina; Resobantin; SC 2910; Ulcine; Ulcudexter; Uldumont; Vagamin;Vagantin; Xanteline; b-Diethylaminoethyl xanthene-9-carboxylate methobromide
Density: g/cm3
Melting Point: 175-176°
Boiling Point: °Cat760mmHg
Flash Point: °C
Safety: Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and subcutaneous routes. Unspecified human reproductive effects. When heated to decomposition it emits very toxic fumes of NOx, NH3, and Br−.
PSA: 35.53000
LogP: 0.95780
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Chemistry

Product Name: Xanthine bromide (CAS NO.53-46-3)


Molecular Formula: C21H26BrNO3
Molecular Weight: 420.34g/mol
Mol File: 53-46-3.mol
H-Bond Donor: 0
H-Bond Acceptor: 4
Rotatable Bond Count: 7
Topological Polar Surface Area: 35.5
Heavy Atom Count: 26
Complexity: 426
Covalently-Bonded Unit Count: 2

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LDLo intravenous 23mg/kg (23mg/kg)   Proceedings of the Society for Experimental Biology and Medicine. Vol. 78, Pg. 576, 1951.
dog LDLo oral 460mg/kg (460mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 104, Pg. 54, 1952.
mouse LD50 intraperitoneal 46mg/kg (46mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 106, Pg. 141, 1952.
mouse LD50 intravenous 4300ug/kg (4.3mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 105, Pg. 221, 1956.
mouse LD50 oral 460mg/kg (460mg/kg)   Drugs in Japan Vol. 6, Pg. 357, 1982.
mouse LDLo subcutaneous 395mg/kg (395mg/kg)   United States Patent Document. Vol. #3714357,
rat LD50 intravenous 4800ug/kg (4.8mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION		 Toxicology and Applied Pharmacology. Vol. 1, Pg. 391, 1959.
rat LD50 oral 400mg/kg (400mg/kg)   Proceedings of the Society for Experimental Biology and Medicine. Vol. 78, Pg. 708, 1951.
rat LDLo subcutaneous 320mg/kg (320mg/kg)   United States Patent Document. Vol. #3714357,

Safety Profile

Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and subcutaneous routes. Unspecified human reproductive effects. When heated to decomposition it emits very toxic fumes of NOx, NH3, and Br−.

Specification

 Xanthine bromide ,its CAS NO. is 53-46-3,the synonyms is  Asabaine ; Avagal ; Banthin ; Banthine ; Bromure de methanthelinum ; Diethyl(2-hydroxyethyl)methylammonium bromide xanthene-9-carboxylate ; Dixamone bromide ; Doladene ; Ethanaminium, N,N-diethyl-N-methyl-2-((9H-xanthen-9-ylcarbonyl)oxy)-, bromide ; Frenogastrico ; Gastron ; Gastrosedan ; Metantelinio bromuro ; Methanide ; Methantheline bromide ; Methanthelinii bromidum ; Vagamin ; Xanteline ; Xanthene-9-carboxylic acid, ester with diethyl(2-hydroxyethyl)methylammonium bromide ; beta-Diethylaminoethyl xanthene-9-carboxylate methobromide ; Ammonium, diethyl(2-hydroxyethyl)methyl-, bromide, xanthene-9-carboxylate ; Ethanaminium, N,N-diethyl-N-methyl-2-((9H-xanthen-9-ylcarbonyl)oxy)-, bromide .