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Name |
Mobutazon |
EINECS | 218-641-1 |
CAS No. | 2210-63-1 | Density | 1.14g/cm3 |
PSA | 49.41000 | LogP | 2.26460 |
Solubility | DMSO (Slightly), Methanol (Slightly) | Melting Point |
102-104°C |
Formula | C13H16 N2 O2 | Boiling Point | °Cat760mmHg |
Molecular Weight | 232.282 | Flash Point | °C |
Transport Information | N/A | Appearance | N/A |
Safety | Moderately toxic by intravenous and intraperitoneal routes. When heated to decomposition it emits toxic fumes of NOx. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
1-Phenyl-4-butyl-3,5-pyrazolidinedione;1-Phenyl-4-butylpyrazolidin-3,5-dione;1-Phenyl-4-n-butyl-3,5-dioxopyrazolidine;2-Phenyl-3,5-dihydroxy-4-butylpyrazolidine;4-Butyl-1-phenyl-3,5-dioxopyrazolidine;4-Butyl-1-phenyl-3,5-pyrazolidinedione;4-Butyl-3,5-dioxo-1-phenyltetrahydropyrazole;Arcobutine;Arcomonol Tablets;Butazone;Mobutazon;Mobutazone;Mobuzon;Mofebutazone;Mofesal;Monazan;Monazon;Monobutyl;Monofen;Monofenew;Monomil;Monophenylbutazone;Monorheumetten;Monozon;Mophebutazone;Mozol;NSC 73725;Reumatox; |
Chemistry informtion about Mobutazon (CAS NO.2210-63-1) is:
IUPAC Name: 4-Butyl-1-Phenylpyrazolidine-3,5-Dione
Synonyms: Mofebutazone ; 2fdbp ; 2-Phenyl-3,5-Dihydroxy-4-Butylpyrazolidine ; 4-Butyl-1-Phenyl-3,5-Dioxopyrazolidine ; 4-Butyl-1-Phenyl-3,5-Pyrazolidinedione ; 4-Butyl-1-Phenyl-5-Pyrazolidinedione ; Arcomonoltablets ; Mobutazon
MF: C13H16N2O2
MW: 232.28
EINECS: 218-641-1
Density: 1.14 g/cm3
Following is the molecular structure of Mobutazon (CAS NO.2210-63-1) is:
Mobutazon (CAS NO.2210-63-1) is a drug used for joint and muscular pain.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 700mg/kg (700mg/kg) | behavioral: tremor behavioral: convulsions or effect on seizure threshold lungs, thorax, or respiration: dyspnea | Scientia Pharmaceutica. Vol. 37, Pg. 185, 1969. |
mouse | LD50 | intravenous | 600mg/kg (600mg/kg) | Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 233, Pg. 365, 1958. | |
mouse | LD50 | subcutaneous | 920mg/kg (920mg/kg) | behavioral: tremor lungs, thorax, or respiration: dyspnea behavioral: convulsions or effect on seizure threshold | Scientia Pharmaceutica. Vol. 37, Pg. 185, 1969. |
rat | LD50 | intraperitoneal | 848mg/kg (848mg/kg) | Farmaco, Edizione Scientifica. Vol. 14, Pg. 347, 1959. | |
rat | LD50 | oral | 1750mg/kg (1750mg/kg) | Pharmaceutica Acta Helvetiae. Vol. 39, Pg. 155, 1964. |
Moderately toxic by intravenous and intraperitoneal routes. When heated to decomposition it emits toxic fumes of NOx.