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| CAS No. | 25339-17-7 |
| Chemical Name: | Isodecanol |
| Synonyms: | isodecyl;Isodecanol;Isodesyl alcohol;Isodecyl alcohol;8-methylnonan-1-ol;8-Methylnonane-1-ol;DECANOL-ISOMERENGEMISCH;DECANOL MIXTURE OF ISOMERS;isodecylalcohol(mixedisomers) |
| CBNumber: | CB7497531 |
| Molecular Formula: | C10H22O |
| Formula Weight: | 158.28 |
| MOL File: | 25339-17-7.mol |
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| Isodecanol Property |
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| density : |
0.838 g/mL at 20 °C |
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| refractive index : |
n20/D 1.440 |
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Isodecanol Chemical Properties,Usage,Production |
General Description
Colorless liquid with a mild alcohol odor. Floats on water. |
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Reactivity Profile
Isodecanol attacks plastics. REF [Handling Chemicals Safely, 1980. p. 236]. Acetyl bromide reacts violently with alcohols or water, [Merck 11th ed., 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid, [Chem. Eng. News 45(43):73(1967); J, Org. Chem. 28:1893(1963)]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites, [NFPA 491 M, 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)]. |
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Health Hazard
Direct contact with skin can produce irritation. |
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| Isodecanol Suppliers Global( 16)Suppliers |
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