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| | Hydroabietyl alcohol Basic information |
| Product Name: | Hydroabietyl alcohol | | Synonyms: | dihydro-abietylalcoho;dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethano;dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-Phenanthrenemethanol;[1R-(1alpha,4abeta,4balpha,10aalpha)]-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol;ABITOL;ABITOL TECH;Dihydroabietyl alcohol (technical mix);Hydroabietyl alcohol 10g [26266-77-3] | | CAS: | 26266-77-3 | | MF: | C20H34O | | MW: | 290.48 | | EINECS: | 247-574-0 | | Product Categories: | | | Mol File: | 26266-77-3.mol |  |
| | Hydroabietyl alcohol Chemical Properties |
| Boiling point | 387.431±11.00 °C(Press: 760.00 Torr)(predicted) | | density | 0.984±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 14.961±0.10(predicted) | | color | A colourless viscous liquid with a very faint wood-like odour | | Odor | mild woody | | Henry's Law Constant | 1.9×10-1 mol/(m3Pa) at 25℃, Zhang et al. (2010) | | Cosmetics Ingredients Functions | VISCOSITY CONTROLLING
BINDING | | InChI | 1S/C20H34O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h12,14-15,17-18,21H,5-11,13H2,1-4H3 | | InChIKey | FLMIYUXOBAUKJM-UHFFFAOYSA-N | | SMILES | CC(C)C1CCC2C(CCC3C(C)(CO)CCCC23C)=C1 | | LogP | 6.789 (est) | | EPA Substance Registry System | 1-Phenanthrenemethanol, 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bS,10aR)- (26266-77-3) |
| WGK Germany | WGK 3 | | TSCA | TSCA listed | | Storage Class | 13 - Non Combustible Solids | | toxicity | Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Shelanski, 1972). |
| | Hydroabietyl alcohol Usage And Synthesis |
| Chemical Properties | The pure hydroabietyl alcohol is almost white, crystalline plates or powder. M.P. 174-182” C. Lower grade commercial material is usually off-white or pale straw-colored, granular crystals or conglomerated mass with much lower melting point. Insoluble in water, soluble in alcohol and oils. Also soluble in aqueous solution of Sodium hydroxide. | | Occurrence | Has apparently not been reported to occur in nature | | Uses | for use in adhesives, mascara, inks, sealants,
etc.; pasticizer in plastic materials; | | Uses | Hydroabietyl alcohol is also the natural source and parent of several solvent-fixatives, used in perfumery: Abitol, Methyl abietate (Abalyn) and hydrogenated Methyl abietate (Hercolyn). Rosin, the natural material, is occasionally used as a fixative in Pine and other fragrance types. It is inexpensive and has at times been popular in certain types of soap perfume. Certain derivatives of Abietic acid are used as emulsifiers and “cloudificators” in carbonated beverages - to give visual impression of fruit juice content in beverages made with little or no “cloudy” natural juice. “Cloudy” Orange sodas are popular in certain countries. | | Preparation | From hydrogenated rosin acids (Arctander, 1969). | | Preparation | By distillation of Rosin (from American Turpentine, e. g.) or by treatment with acid to isomenze the natural Levopimaric acid. Purification over the Diamylammonium salt. |
| | Hydroabietyl alcohol Preparation Products And Raw materials |
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