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| | triclobisonium chloride Basic information |
| Product Name: | triclobisonium chloride | | Synonyms: | 6-[dimethyl-[4-(2,2,6-trimethylcyclohexyl)butan-2-yl]azaniumyl]hexyl-dimethyl-[4-(2,2,6-trimethylcyclohexyl)butan-2-yl]azanium dichloride;triclobisonium chloride;Triclobisonium;Ro-5-0810/1;Triburon;Triclobisonium dichloride;6-[dimethyl-[1-methyl-3-(2,2,6-trimethylcyclohexyl)propyl]ammonio]hexyl-dimethyl-[1-methyl-3-(2,2,6-trimethylcyclohexyl)propyl]ammonium dichloride | | CAS: | 79-90-3 | | MF: | C36H74N2.2Cl | | MW: | 605.901 | | EINECS: | 201-232-7 | | Product Categories: | | | Mol File: | 79-90-3.mol |  |
| | triclobisonium chloride Chemical Properties |
| Melting point | 243-253° (dec) | | color | White, crystalline powder |
| Toxicity | LD50 orl-mus: 375 mg/kg ANTCAO 9,267,59 |
| | triclobisonium chloride Usage And Synthesis |
| Originator | Triburon,Roche,US,1959 | | Manufacturing Process | To a solution of 49 grams (0.25 mol) of cis-tetrahydroionone and 14.1 grams
(0.12 mol) of 1,6-hexanediamine in 150 ml of ethanol was added 1 teaspoon
of Raney nickel. The volume was adjusted to 300 ml with ethanol and the
mixture was hydrogenated at 50°C and a pressure of 200 psi. The catalyst
was filtered off, the filtrate was concentrated and the residual oil fractionated
in vacuo to obtain N,N'-bis[1-methyl-3-(2,2,6-trimethylcyclohexyl)propyl]-1,6-
hexanediamine; BP 192° to 202°C at 0.02 mm.
To 217 grams (0.456 mol) of N,N'-bis[1-methyl-3-(2,2,6-
trimethylcyclohexyl)propyl]-1,6-hexanediamine were added 182 ml (3.04
mols) of formic acid (90%). The resulting colorless solution was cooled, then
91.3 ml (1.043 mols) of formaldehyde (37%) were added. The solution was
heated at steam temperature with occasional shaking for 2 hours and then
refluxed for 8 hours. The volatiles were distilled off at steam temperature
under water vacuum and the residual oil was made strongly alkaline with 50%
potassium hydroxide. The reaction product was extracted with ether. The
ether extract was washed with water, dried and concentrated in vacuo. The
residual oil was fractionated in vacuo to obtain N,N'-bis[1-methyl-3-(2,2,6-
trimethylcyclohexyl)propyl]-N,N'-dimethyl-1,6-hexanediamine, BP0.4 230° to
240°C, nD26 = 1.4833. An aliquot, when treated with an ethanolic hydrogen
chloride, gave the crystalline dihydrochloride, MP 183° to 185°C (recrystallized
from ethanol-acetonitrile).
To 5 grams of N,N'-bis[1-methyl-3-(2,2,6-trimethylcyclohexyl)propyl]-N,N'-
dimethyl-1,6-hexanediamine dissolved in 100 ml of methanol, at 4°C. were
added 100 ml methanol containing 10 grams of methyl chloride. The solution
was heated in a closed vessel at 60°C for 15 hours. The colorless solution was concentrated and the resulting white solid crystallized from ethanol_x0002_acetonitrile-ether to obtain N,N'-bis[1-methyl-3-(2,2,6-
trimethylcyclohexyl)propyl]-N,N'-dimethyl-1,6-hexanediamine
bis(methochloride) hemihydrate. | | Therapeutic Function | Antiseptic | | Safety Profile | Poison by ingestion,subcutaneous, intravenous, and intraperitoneal routes.When heated to decomposition it emits toxic fumes of Clíand NOx. |
| | triclobisonium chloride Preparation Products And Raw materials |
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