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CAS No.: | 27959-26-8 |
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Name: | Nicomol |
Article Data: | 2 |
Molecular Structure: | |
Formula: | C34H32 N4 O9 |
Molecular Weight: | 640.649 |
Synonyms: | 3-Pyridinecarboxylicacid, (2-hydroxy-1,3-cyclohexanediylidene)tetrakis(methylene) ester (9CI);Nicotinic acid, 1,1,3,3-tetraester with2-hydroxy-1,1,3,3-cyclohexanetetramethanol (7CI,8CI);1,1,3,3-Cyclohexanetetramethanol, 2-hydroxy-, 1,1,3,3-tetranicotinate (8CI);2,2,6,6-Tetrakis(nicotinoyloxymethyl)cyclohexanol; Cholexamine; K 31; K 31(pharmaceutical); Nicomol |
EINECS: | 248-748-9 |
Density: | 1.316g/cm3 |
Melting Point: | 177-180° |
Boiling Point: | 763.3°Cat760mmHg |
Flash Point: | 415.4°C |
Safety: | Mildly toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx. An anticholesteremic agent that reduces the blood cholesterol level. See also ESTERS. |
PSA: | 176.99000 |
LogP: | 3.51200 |
Chemistry informtion about Cholexamin (CAS NO.27959-26-8) is:
IUPAC Name: [2-Hydroxy-1,3,3-Tris(Pyridine-3-Carbonyloxymethyl)Cyclohexyl]Methyl Pyridine-3-Carboxylate
Synonyms: [2-Hydroxy-1,3,3-Tris(Pyridine-3-Carbonyloxymethyl)Cyclohexyl]Methyl Pyridine-3-Carboxylate ; Nicomol ; 2,2,6,6-Tetrakis(Nicotinoyloxymethyl)Cyclohexanol ; 2-Hydroxy-1,1,3,3-Cyclohexanetetramethanol 1,1,3,3-Tetranicotinate ; Atomirate ; Cholexamin ; K-31
MF: C34H32N4O9
MW: 640.63928
EINECS: 248-748-9
Density: 1.316 g/cm3
Flash Point: 415.4 °C
Boiling Point: 763.3 °C at 760 mmHg
Vapour Pressure: 1.71E-24 mmHg at 25°C
Enthalpy of Vaporization: 116.63 kJ/mol
Following is the molecular structure of Cholexamin (CAS NO.27959-26-8) is:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
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mouse | LD50 | intraperitoneal | > 14700mg/kg (14700mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 2, Pg. 237, 1968. | |
mouse | LD50 | oral | > 17800mg/kg (17800mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 2, Pg. 237, 1968. | |
mouse | LD50 | subcutaneous | > 3gm/kg (3000mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 2, Pg. 237, 1968. | |
rat | LD20 | intraperitoneal | > 2500mg/kg (2500mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 14(5), Pg. 741, 1977. | |
rat | LD50 | oral | 10gm/kg (10000mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 14, Pg. 741, 1977. | |
rat | LD50 | subcutaneous | > 3gm/kg (3000mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 2, Pg. 237, 1968. |
Mildly toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx. An anticholesteremic agent that reduces the blood cholesterol level. See also ESTERS.