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LINALYL PHENYL ACETATE

Product Name
LINALYL PHENYL ACETATE
CAS No.
7143-69-3
Chemical Name
LINALYL PHENYL ACETATE
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-ethenyl-1,5-dimethyl-4-hexenylester;benzeneaceticacid,1,5-dimethyl-1-ethenyl-4-hexenylester;Phenylacetic acid 3,7-dimethyl-1,6-octadiene-3-yl ester;Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
CBNumber
CB2345785
Molecular Formula
C18H24O2
Formula Weight
272.38
MOL File
7143-69-3.mol
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LINALYL PHENYL ACETATE Property

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
Odor
at 100.00 %. rose sweet honey sick neroli rose
Odor Type
floral
JECFA Number
1019
LogP
5.64
EPA Substance Registry System
Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexenyl ester (7143-69-3)
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Safety

Toxicity
Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg(Moreno, 1974).
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
FFG0000672
Product name
LINALYL PHENYL ACETATE
Purity
98.00%
Packaging
50G
Price
$3542.39
Updated
2021/12/16
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LINALYL PHENYL ACETATE Chemical Properties,Usage,Production

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

Raw materials

Preparation Products

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LINALYL PHENYL ACETATE Suppliers

Shanghai wencai New Material Technology Co., Ltd.
Tel
15721586846
Fax
15721586846
Email
wencaimat@163.com
Country
China
ProdList
2796
Advantage
58
TCI (Shanghai) Chemical Trading Co., Ltd.
Tel
021-61109150
Fax
021-61105897
Email
sales@tcisct.com
Country
China
ProdList
31163
Advantage
58
Shaanxi Dideu Newmaterial Co., Ltd.
Tel
029-63373950 15353716720
Email
1052@dideu.com
Country
China
ProdList
10008
Advantage
58

7143-69-3, LINALYL PHENYL ACETATERelated Search:


  • 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
  • Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
  • 7143-69-3