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| CAS No.: | 1190-53-0 |
|---|---|
| Name: | BUTYL-BIGUANIDE HYDROCHLORIDE |
| Article Data: | 1 |
| Molecular Structure: | |
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| Formula: | C6H15 N5 . Cl H |
| Molecular Weight: | 193.68 |
| 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 |
| EINECS: | 214-723-6 |
| Melting Point: | 174-177ºC |
| Boiling Point: | 322.7 °C at 760 mmHg |
| Flash Point: | 148.9 °C |
| Solubility: | Freely sol in water, alcohol |
| Risk Codes: | 22-43-36 |
| Safety: | A poison via ingestion, intravenous, and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of HCl and NOx. |
| PSA: | 97.78000 |
| LogP: | 2.27750 |
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Chemistry
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:
Toxicity Data With Reference
| 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. |
Safety Profile
A poison via ingestion, intravenous, and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of HCl and NOx.