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1118-27-0

1118-27-0 Structure

1118-27-0 Structure
IdentificationBack Directory
[Name]

LINALYL ISOVALERATE
[CAS]

1118-27-0
[Synonyms]

FEMA 2646
LINALYL ISOVALERATE
1,5-dimethyl-1-vinylhex
Linalyl isovalerate ester
LINALYL ISOVALERATE 95+%
Linalyl isovalerate >=95%, FG
LINALYL ISOVALERATE USP/EP/BP
Isovaleric acid linalyl ester
1,5-dimethyl-1-vinylhex-4-enyl
linalylisovalerate,linalylisopentanoate
1,5-Dimethyl-1-vinylhex-4-enylisovalerat
6-octadien-3-ol,4,7-dimethyl-isovalerate
1,5-dimethyl-1-vinylhex-4-enylisovalerate
3,7-dimethyl-1,6-octadien-3-ylisovalerate
1,5-Dimethyl-1-vinyl-4-hexenyl 3-methylbutanoate
Isovaleric acid 1,5-dimethyl-1-vinyl-4-hexenyl ester
isovalericacid,(4,7-dimethyl-1,6-octadien-3-yl)ester
Butanoicacid,3-methyl-,1-ethenyl-1,5-dimethyl-4-hexenylester
Butanoic acid, 3-methyl-, 1-ethenyl-1,5-dimethyl-4-hexenyl ester
Butanoic acid, 3-methyl-, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
[EINECS(EC#)]

214-259-4
[Molecular Formula]

C15H26O2
[MDL Number]

MFCD00048304
[MOL File]

1118-27-0.mol
[Molecular Weight]

238.37
Chemical PropertiesBack Directory
[Boiling point ]

188 °C(lit.)
[density ]

0.885 g/mL at 25 °C(lit.)
[FEMA ]

2646 | LINALYL ISOVALERATE
[refractive index ]

n20/D 1.451(lit.)
[Fp ]

229 °F
[Odor]

at 100.00 %. citrus bergamot lavender peach apricot sage
[Odor Type]

herbal
[JECFA Number]

363
[LogP]

5.24
[EPA Substance Registry System]

Butanoic acid, 3-methyl-, 1-ethenyl-1,5-dimethyl-4-hexenyl ester (1118-27-0)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

2
[RTECS ]

RG5927200
Hazard InformationBack Directory
[Description]

Linalyl isovalerate has a stable, suave, fruity odor and a sweet, apple-like taste somewhat reminiscent of plum and peach. May be synthesized from dehydrolinalool and isovaleric acid followed by hydrogenation; also from linalool and isovaleric acid by azeotropic esterification.
[Chemical Properties]

Linalyl isovalerate has a stable, suave, fruity odor and a sweet, apple-like taste somewhat reminiscent of plum and peach.
[Occurrence]

Reported found in nature (Salvia officinalis and Salvia spinosa).
[Preparation]

From dehydrolinalool and isovaleric acid followed by hydrogenation; also from linalool and isovaleric acid by azeotropic esterification.
Spectrum DetailBack Directory
[Spectrum Detail]

LINALYL ISOVALERATE(1118-27-0)FT-IR
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