| Identification | Back Directory | [Name]
LINALYL PHENYL ACETATE | [CAS]
7143-69-3 | [Synonyms]
Linalylphenylacetat
linalylalpha-toluate
LINALYL PHENYL ACETATE
3,7-dimethylocta-1,6-dien-3-yl 2-phenylacetate
aceticacid,phenyl-,1,5-dimethyl-1-vinyl-4-hexenylester
benzeneaceticacid,1,5-dimethyl-1-ethenyl-4-hexenylester
Benzeneaceticacid,1-ethenyl-1,5-dimethyl-4-hexenylester
Phenylacetic acid 3,7-dimethyl-1,6-octadiene-3-yl ester | [EINECS(EC#)]
230-444-2 | [Molecular Formula]
C18H24O2 | [MDL Number]
MFCD00036649 | [MOL File]
7143-69-3.mol | [Molecular Weight]
272.38 |
| Safety Data | Back Directory | [TSCA ]
TSCA listed | [Toxicity]
Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg(Moreno, 1974). |
| Hazard Information | Back Directory | [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) |
| Questions And Answer | Back Directory | [Aroma]
Mildly floral, intensely sweet Neroli-Rose
type odor of great tenacity and with variable
amounts of Honey-like undertones, according
to origin of sample or method of production. |
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BOC Sciences
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https://www.bocsci.com |
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