CAS 13393-93-6
:(1R,4aR,4bS,10aR)-Tetradecahidro-1,4a-dimetil-7-(1-metiletil)-1-fenantrenometanol
- (1R,4aR,4bS,10aR)-Tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethanol
- (8Xi,13Xi)-Abietan-18-Ol
- 1-Phenanthrenemethanol, tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-
- 1-Phenanthrenemethanol, tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bS,10aR)-
- Abietan-18-Ol
- Abietyl alcohol, tetrahydro-
- Hydroabietyl Alcohol Primary Alcohol
- Tetradecahydro-1,4A-Dimethyl-7-(1-Methylethyl)-1-Phenanthrenemethano
- Tetradecahydro-7-Isopropyl-1,4A-Dimethylphenanthren-1-Methanol
- Tetrahydroabietyl Alcohol)
- tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-Phenanthrenemethanol
- (8X,13X)-Abietan-18-ol
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Tetrahydroabietyl Alcohol
CAS:Producto controladoApplications Tetrahydroabietyl Alcohol, is a fragrance raw material, used in the perfumery industry.
References Opdyke, D. L. J., Food and Cosmetics Toxicology, 12, 919 (1974)Fórmula:C20H36OForma y color:NeatPeso molecular:292.5Tetrahydroabietyl alcohol
CAS:Producto controladoTetrahydroabietyl alcohol is a colorless liquid that is soluble in water and has a molecular weight of 150. It belongs to the group of hydroxy-substituted monomers. Tetrahydroabietyl alcohol can be used as a raw material for polyesters, polyurethanes, and other industrial chemicals. It can be produced by the reaction of an aromatic hydrocarbon with phosphite followed by hydrolysis. The product can also be synthesized from hexane fatty alcohols or acid catalysts, such as monocarboxylic acids. This compound is used for stabilizing ester compounds and terpene esters. Tetrahydroabietyl alcohol can also be obtained by hydrogenation of terpenes and their derivatives under high pressure and temperature conditions in the presence of metal catalysts, such as palladium or platinum.
Fórmula:C20H36OPureza:Min. 95%Peso molecular:292.5 g/molRef: 3D-FT162576
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