Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
Buformin hydrochloride |
EINECS | 214-723-6 |
CAS No. | 1190-53-0 | Density | N/A |
PSA | 97.78000 | LogP | 2.27750 |
Solubility | Freely sol in water, alcohol | Melting Point |
174-177ºC |
Formula | C6H15 N5 . Cl H | Boiling Point | 322.7 °C at 760 mmHg |
Molecular Weight | 193.68 | Flash Point | 148.9 °C |
Transport Information | N/A | Appearance | N/A |
Safety | A poison via ingestion, intravenous, and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of HCl and NOx. | Risk Codes | 22-43-36 |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Biguanide,1-butyl-, monohydrochloride (8CI); Imidodicarbonimidic diamide, N-butyl-,monohydrochloride (9CI); 1-Butylbiguanide hydrochloride; 1-Butylbiguanide,monohydrochloride; 1-Butyldiguanide hydrochloride; Andere; Biforon; Bigunal;Bufonamin; Buformin hydrochloride; Bulbonin; Diabrin; Dibetos; Glibutide;Gliporal; Glybutide; Insulamin; Krebon; N-Butylbiguanide hydrochloride;N1-Butyl-biguanide hydrochloride; N1-n-Butylbiguanide hydrochloride; Panformin;Sindiatil; Tidemol; Ziavetine |
Article Data | 1 |
Chemistry informtion about N-Butylbiguanide Hydrochloride (CAS NO.1190-53-0) is:
IUPAC Name: 2-Butyl-1-(Diaminomethylidene)Guanidine
Synonyms: Buformine Hcl ; Buformine Hydrochloride ; Butyl-Biguanide Hydrochloride ; N-Butyl Biguanide Hydrochloride ; 1-Butylbiguanide Monohydrochloride ; N-Butylbiguanidehcl ; 1-Butylbigyanidine Hydrochloride
MF: C6H16ClN5
MW: 193.68
EINECS: 214-723-6
Flash Point: 148.9 °C
Boiling Point: 322.7 °C at 760 mmHg
Vapour Pressure: 0.000275 mmHg at 25°C
Enthalpy of Vaporization: 56.45 kJ/mol
Following is the molecular structure of N-Butylbiguanide Hydrochloride (CAS NO.1190-53-0) is:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
guinea pig | LD50 | oral | 58mg/kg (58mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 12, Pg. 314, 1962. | |
guinea pig | LD50 | subcutaneous | 23mg/kg (23mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 12, Pg. 314, 1962. | |
human | TDLo | oral | 2857ug/kg (2.857mg/kg) | blood: other changes | Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 7, Pg. 1504, 1965. |
mouse | LD50 | intraperitoneal | 74mg/kg (74mg/kg) | behavioral: somnolence (general depressed activity) behavioral: convulsions or effect on seizure threshold lungs, thorax, or respiration: respiratory stimulation | Toksikologicheskii Vestnik. Vol. (2), Pg. 41, 1993. |
mouse | LD50 | intravenous | 105mg/kg (105mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 12, Pg. 314, 1962. | |
mouse | LD50 | oral | 380mg/kg (380mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 12, Pg. 314, 1962. | |
rat | LD50 | oral | 320mg/kg (320mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 12, Pg. 314, 1962. |
A poison via ingestion, intravenous, and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of HCl and NOx.