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Linalyl phenyl acetate

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Linalyl phenyl acetate Basic information
Aroma
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;Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
CAS:7143-69-3
MF:C18H24O2
MW:272.38
EINECS:230-444-2
Product Categories:
Mol File:7143-69-3.mol
Linalyl phenyl acetate Structure
Linalyl phenyl acetate Chemical Properties
Boiling point 375.44°C (rough estimate)
density 1.0134 (rough estimate)
refractive index 1.5510 (estimate)
FEMA 3501 | LINALYL PHENYLACETATE
color A colourless or pale straw-coloured viscous liquid
Odorat 100.00 %. rose sweet honey sick neroli rose
Odor Typefloral
JECFA Number1019
Cosmetics Ingredients FunctionsPERFUMING
LogP5.64
EPA Substance Registry SystemBenzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexenyl ester (7143-69-3)
Safety Information
TSCA TSCA listed
toxicityBoth the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg(Moreno, 1974).
MSDS Information
Linalyl phenyl acetate Usage And Synthesis
AromaMildly 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.
DescriptionLinalyl 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 PropertiesLinalyl phenylacetate has a mildly floral, intensely sweet Neroli rose–type odor.
OccurrenceHas apparently not been reported to occur in nature
DefinitionChEBI: Linalyl phenylacetate is a monoterpenoid.
PreparationFrom dehydrolinalool and methyl phenylacetate in the presence of sodium methylate catalyst, followed by hydrogenation of the ester, or by any other suitable means.
MetabolismOpen-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
Tag:Linalyl phenyl acetate(7143-69-3) Related Product Information
6-METHYL-5-HEPTEN-2-OL Linalool ALLYL PHENYLACETATE LINALYL PROPIONATE 2-Methyl-3-buten-2-ol MYCOLIDE 1,6-Octadiene PETIOLE Linalyl acetate 1-Hexen-3-yl acetate Linalyl phenyl acetate tert-Butyl propionate 3-Methyl-1-penten-3-ol FEMA 2955 LINALYL FORMATE 7-Methyl-1,6-octadiene Isopropyl phenylacetate Butyl phenylacetate