ChemicalBook--->CAS DataBase List--->7493-78-9

7493-78-9

7493-78-9 Structure

7493-78-9 Structure
IdentificationBack Directory
[Name]

ALPHA-N-AMYL CINNAMYL ACETATE
[CAS]

7493-78-9
[Synonyms]

AMYLCINNAMYLACETATE
AMYL CINNAMIC ACETATE
α-Amylcinnamyl Acetate
alpha-amylcinnamylacetate
alpha-pentylcinnamylacetate
2-BENZYLIDENEHEPTYL ACETATE
ALPHA-N-AMYL CINNAMYL ACETATE
2-(Phenylmethylen)heptylacetat
2-benzylidene-1-heptanoacetate
2-(phenylmethylene)heptyl acetate
alpha-pentyl-cinnamylalcohoacetate
Acetic acid α-pentylcinnamyl ester
2-(phenylmethylene)-1-heptanoacetate
alpha-n-amyl-beta-phenylacrylacetate
1-Heptanol, 2-(phenylmethylene)-, acetate
1-Heptanol,2-(phenylmethylene)-, 1-acetate
[EINECS(EC#)]

231-339-4
[Molecular Formula]

C16H22O2
[MDL Number]

MFCD00026207
[MOL File]

7493-78-9.mol
[Molecular Weight]

246.34
Chemical PropertiesBack Directory
[Boiling point ]

329.35°C (rough estimate)
[density ]

1.0594 (rough estimate)
[FEMA ]

2064 | ALPHA-AMYLCINNAMYL ACETATE
[refractive index ]

1.4700 (estimate)
[color ]

A colourless oily liquid.
[Odor]

at 100.00 %. floral jasmin chocolate leather fruity balsam spicy cinnamyl
[Odor Type]

floral
[JECFA Number]

677
[LogP]

5.09
[EPA Substance Registry System]

1-Heptanol, 2-(phenylmethylene)-, acetate (7493-78-9)
Safety DataBack Directory
[HS Code ]

2918195000
[Toxicity]

skn-rbt 500 mg/24H FCTXAV 14,659,76
Hazard InformationBack Directory
[Chemical Properties]

α-Amylcinnamyl acetate has a mild fruity, green odor with a balsamic and slightly floral undernote; somewhat fruity flavor.
[Occurrence]

Has apparently not been reported to occur in nature.
[Uses]

α-Amylcinnamyl Acetate can be used for fragrant substances for hair cosmetics.
[Preparation]

From amyl cinnamic alcohol and acetic acid under azeotropic conditions
[Taste threshold values]

Taste characteristics at 15 ppm: earthy, fruity, spicy, powdery and balsamic.
[Safety Profile]

Moderately toxic skin irritant.When heated to decomposition it emits acrid smoke andirritating fumes.
[Metabolism]

Cinnamic alcohol is mainly metabolized to benzoic acid, presumably via cinnamic acid. Substitution apparently prevents oxidation to benzoic acid, since 2-ethylcinnamic alcohol is partly excreted as α-ethylcinnamic acid (30-33% in rabbits) (Williams, 1959).
Questions And AnswerBack Directory
[Aroma]

Mild oily -fruity and somewhat green odor with balsamic and faintly floral undertones. Finds but little use in perfumery, mainly as a modifier for floral-green components of Jasmin and other floral complexes. Occasionally used in flavor compositions, for imitation Chocolate, Fruit and Honey flavors - usually in traces only.
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