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15351-05-0

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Basic Information
CAS No.: 15351-05-0
Name: buzepide metiodide
Molecular Structure:
Molecular Structure of 15351-05-0 (buzepide metiodide)
Formula: C23H31 N2 O . I
Molecular Weight: 478.416
Synonyms: 1-(3-Carbamoyl-3,3-diphenylpropyl)hexahydro-1-methylazepiniumiodide (6CI); 1H-Azepinium,1-(3-carbamoyl-3,3-diphenylpropyl)hexahydro-1-methyl-, iodide (8CI);1H-Azepinium, 1-(4-amino-4-oxo-3,3-diphenylbutyl)hexahydro-1-methyl-, iodide(9CI); 1-(3-Carbamoyl-3,3-diphenylpropyl) perhydro-1-methylazepinium iodide;2,2-Diphenyl-4-hexamethyleniminobutyramide methiodide; Buzepide methiodide;Buzepide metiodide; Difexamide methiodide; Diphexamide methiodide; FI 6146;Metazepium iodide; R 661; Spactin
Melting Point: 212-213 °C (decomp)
Safety: A poison by intraperitoneal, intravenous, intramuscular, and subcutaneous routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of I− and NOx. See also IODIDES.
PSA: 43.09000
LogP: 1.53180
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Chemistry

IUPAC Name: 4-(1-Methylazepan-1-ium-1-yl)-2,2-diphenylbutanamide iodide
Synonyms of Buzepide methiodide (CAS NO.15351-05-0): Buzepide metiodide ; Buzepide metiodide [INN:DCF] ; 2,2-Diphenyl-4-N-hexamethyleniminobutyramide methiodide ; Buzepidi metiodidum ; Buzepidi metiodidum [INN-Latin] ; Difexamide methiodide ; Diphexamide methiodide ; EINECS 239-383-6 ; FI 6146 ; Metiodure de buzepide ; Metiodure de buzepide [INN-French] ; Metioduro de buzepida ; Metioduro de buzepida [INN-Spanish] ; R 661 ; Spactin ; UNII-5A9SS67K16 ; 1-(3-Carbamoyl-3,3-diphenylpropyl)perhydro-1-methylazepinium iodide ; 1-(4-Amino-4-oxo-3,3-diphenylbutyl)hexahydro-1-methyl-1H-azepinium iodide ; 1H-Azepinium, hexahydro-1-(3-carbamoyl-3,3-diphenylpropyl)-1-methyl-, iodide
CAS NO: 15351-05-0    
Molecular Formula of Buzepide methiodide (CAS NO.15351-05-0): C23H31IN2O 
Molecular Weight of Buzepide methiodide (CAS NO.15351-05-0): 478.4095  
H bond acceptors: 3
H bond donors: 2
Freely Rotating Bonds: 6
Polar Surface Area: 20.31 Å2
Molecular Structure:

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intramuscular 201mg/kg (201mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: TREMOR

BEHAVIORAL: ATAXIA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
mouse LD50 intraperitoneal 94mg/kg (94mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: TREMOR

LUNGS, THORAX, OR RESPIRATION: DYSPNEA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
mouse LD50 intravenous 14mg/kg (14mg/kg) SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE

LUNGS, THORAX, OR RESPIRATION: DYSPNEA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
mouse LD50 oral 820mg/kg (820mg/kg) BEHAVIORAL: MUSCLE WEAKNESS Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
mouse LD50 subcutaneous 229mg/kg (229mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
rat LD50 intramuscular 800mg/kg (800mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: ATAXIA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
rat LD50 intraperitoneal 145mg/kg (145mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
rat LD50 intravenous 29300ug/kg (29.3mg/kg) SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE

LUNGS, THORAX, OR RESPIRATION: DYSPNEA		 Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
rat LD50 oral 2800mg/kg (2800mg/kg) BEHAVIORAL: MUSCLE WEAKNESS Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.
rat LD50 subcutaneous 1210mg/kg (1210mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 1850, 1970.

Safety Profile

A poison by intraperitoneal, intravenous, intramuscular, and subcutaneous routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of I− and NOx. See also IODIDES.