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| | LINALYL PHENYL ACETATE Basic information |
| Product Name: | LINALYL PHENYL ACETATE | | Synonyms: | aceticacid,phenyl-,1,5-dimethyl-1-vinyl-4-hexenylester;benzeneaceticacid,1,5-dimethyl-1-ethenyl-4-hexenylester;3,7-dimethylocta-1,6-dien-3-yl 2-phenylacetate;Benzeneaceticacid,1-ethenyl-1,5-dimethyl-4-hexenylester;linalylalpha-toluate;Linalylphenylacetat;Phenylacetic acid 3,7-dimethyl-1,6-octadiene-3-yl ester;LINALYL PHENYL ACETATE | | CAS: | 7143-69-3 | | MF: | C18H24O2 | | MW: | 272.38 | | EINECS: | 230-444-2 | | Product Categories: | | | Mol File: | 7143-69-3.mol |  |
| | LINALYL PHENYL ACETATE Chemical Properties |
| toxicity | Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg(Moreno, 1974). |
| | LINALYL PHENYL ACETATE Usage And Synthesis |
| Description | Linalyl phenylacetate has a mildly floral, intensely sweet Neroli rose type odor. May be synthesized from dehydrolinalool and
methyl phenylacetate in the presence of sodium methylate catalyst,
followed by hydrogenation of the ester, or by any other suitable
means. | | Chemical Properties | Linalyl phenylacetate has a mildly floral, intensely sweet Neroli rose–type odor. | | Occurrence | Has apparently not been reported to occur in nature | | Definition | ChEBI: Linalyl phenylacetate is a monoterpenoid. | | Preparation | From dehydrolinalool and methyl phenylacetate in the presence of sodium methylate catalyst, followed by hydrogenation
of the ester, or by any other suitable means. | | Metabolism | Open-chain olefinic terpene esters are presumably hydrolysed to the alcohol and the acid (Fassett, 1963). Open-chain terpenes are metabolized in the rabbit by ω-oxidation and by reduction of an a,B-double bond (Williams, 1959) |
| | LINALYL PHENYL ACETATE Preparation Products And Raw materials |
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