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LINALYL CINNAMATE

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LINALYL CINNAMATE Basic information

Product Name:
LINALYL CINNAMATE
Synonyms:
  • 1,5-dimethyl-1-vinyl-4-hexen-1-ocinnamate
  • 1,5-dimethyl-1-vinyl-4-hexen-1-ylcinnamate
  • 2-propenoicacid,3-phenyl-,1,5-dimethyl-1-vinyl-4-hexen-1-ylester
  • 2-Propenoicacid,3-phenyl-,1-ethenyl-1,5-dimethyl-4-hexenylester
  • LINALYL CINNAMATE
  • FEMA 2641
  • 3,7-DIMETHYLOCTA-1,6-DIEN-3-YL (2E)-3-PHENYLPROP-2-ENOATE
  • 3-phenyl-2-propenoicacid,1,5-dimethyl-1-vinyl-4-hexen-1-ylester
CAS:
78-37-5
MF:
C19H24O2
MW:
284.39
EINECS:
201-110-3
Product Categories:
  • ester Flavor
Mol File:
78-37-5.mol
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LINALYL CINNAMATE Chemical Properties

Boiling point:
396℃
Density 
0.989
refractive index 
1.4709 (estimate)
FEMA 
2641 | LINALYL CINNAMATE
Flash point:
216℃
storage temp. 
2-8°C
color 
An almost colourless oily or slightly viscous liquid
Odor
at 100.00 %. sweet balsam lily neroli labdanum amber
Odor Type
balsamic
JECFA Number
668
LogP
6.04
CAS DataBase Reference
78-37-5
EPA Substance Registry System
2-Propenoic acid, 3-phenyl-, 1-ethenyl-1,5-dimethyl-4-hexenyl ester (78-37-5)
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Safety Information

Toxicity
The acute oral LD50 value in rats was reported as 9.96 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964). The acute dermal LD50 value in rabbits exceeded 5 g/kg
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LINALYL CINNAMATE Usage And Synthesis

Description

Linalyl cinnamate has a sweet, persistent odor with soft floral notes. It is clearly balsamic. It has a slightly fruity flavor. May be synthesized from linalyl formate plus methylcinnamate and sodium linalool: by "Roche" method from dehydrolinalool and cinnamic acid via the dehydro ester, which is hydrolyzed to the subject compound.

Chemical Properties

Linalyl cinnamate has a sweet, persistent odor with soft floral notes; clearly balsamic. It has a slightly fruity flavor.

Occurrence

Has apparently not been reported to occur in nature

Uses

It is used as a fragrance in soaps, detergents, creams, lotions, and perfumes.

Definition

ChEBI: Linalyl cinnamate is a cinnamate ester.

Preparation

From linalyl formate plus methylcinnamate and sodium linalool; by “Roche” method from dehydrolinalool and cinnamic acid via the dehydro ester, which is hydrolyzed to the subject compound.

Production Methods

Linayl cinnamate is formed from the reaction of linayl formate with methyl cinnamate and linalool sodium or from the reaction of dehydrolinalool with cinnamic acid.

LINALYL CINNAMATESupplier

3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Syntechem Co.,Ltd
Tel
Email
info@syntechem.com
Amadis Chemical Company Limited
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571-89925085
Email
sales@amadischem.com
Shanghai wencai New Material Technology Co., Ltd.
Tel
15721586846
Email
wencaimat@163.com
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com