ChemicalBook--->CAS DataBase List--->80-25-1

80-25-1

80-25-1 Structure

80-25-1 Structure
IdentificationBack Directory
[Name]

DIHYDROTERPINYL ACETATE
[CAS]

80-25-1
[Synonyms]

MENTHANYL ACETATE
P-MENTHAN-8-YL ACETATE
p-menthan-8-ol,acetate
p-Menthan-8-ol, acetate
DIHYDROTERPINYL ACETATE
P-MENTHANOL-8-OL ACETATE
PARA-MENTHAN-8-OL,ACETATE
dihydro-alpha-terpinylacetate
aceticacid,p-menthan-8-olester
aceticacid,dihydroterpinylester
Acetic acid p-menthan-8-yl ester
Acetic acid, p-menthan-8-ol ester
Acetic acid, dihydroterpinyl ester
2-(4-methylcyclohexyl)propan-2-yl acetate
2-(4-methylcyclohexyl)propan-2-yl ethanoate
1-Methyl-1-(4-methylcyclohexyl)ethyl acetate
alpha,alpha,4-Trimethylcyclohexylmethylacetat
alpha,alpha,4-trimethylcyclohexylmethyl acetate
alpha,alpha,4-trimethyl-cyclohexanemethanoacetate
alpha,alpha,4-Trimethylcyclohexanemethanol acetate
Acetic acid 1-methyl-1-(4-methylcyclohexyl)ethyl ester
CYCLOHEXANE METHANOL, ALPHA, ALPHA-4-TRIMETHYL: ACETATE
[EINECS(EC#)]

201-264-1
[Molecular Formula]

C12H22O2
[MDL Number]

MFCD00013761
[MOL File]

80-25-1.mol
[Molecular Weight]

198.3
Chemical PropertiesBack Directory
[Boiling point ]

275.63°C (rough estimate)
[density ]

0.9694 (rough estimate)
[refractive index ]

1.4460 (estimate)
[color ]

A colourless liquid with a somewhat herbaceous-like odour
[Odor]

at 100.00 %. fresh herbal woody lime cologne soapy
[Odor Type]

woody
[Cosmetics Ingredients Functions]

PERFUMING
[LogP]

4.057 (est)
[EPA Substance Registry System]

Cyclohexanemethanol, .alpha.,.alpha.,4-trimethyl-, acetate (80-25-1)
Safety DataBack Directory
[TSCA ]

TSCA listed
[Toxicity]

The acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1973).
Hazard InformationBack Directory
[Chemical Properties]

Dihydroterpinyl acetate is a colorless liquid, almost insoluble in water, soluble in alcohol and oils. Sp.Gr. 0.94. Fresh-piney, citrusy and somewhat herbaceous odor. Sweeter and fruitier than Terpinyl acetate, the Dihydro terpinylacetate seems to be cool and warm at the same time (minty-camphoraceous, herbaceous). Its tenacity is not very outstanding.
[Occurrence]

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

This ester is used quite widely in perfumery, particularly in low-cost Lavender, Citrus, FougeYes, etc. for detergents and other household products, and in lower cost Colognes, room-sprays, etc. It constitutes an excellent blender for Linalylacetate, Dihydromyrcenol, lsobomylacetate and many other fresh-piney-fruity or citrusy base chemicals.
[Preparation]

By hydrogenation of terpinyl acetate (Arctander, 1969; Bedoukian, 1967).
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