

Available forms:clear liquid
pd_proNo:383907-839c91d9-25ae-44db-8896-a8992a2722cf
pd_productuse:
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Physical properties |
Terpinyl acetate is a p-menthane monoterpenoid that naturally found in melanoleuca, elettaria cardamomum. It is a colorless liquid with a bergamot, bergamot odor. Soluble in five or more volumes of 70% alcohol; slightly soluble in water and glycerol. Combustible. |
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Preparation |
Terpinyl acetate was successfully synthesized from (x-terpineol and acetic anhydride in supercritical carbon dioxide (SC-C02) by enzymatic catalysis.By acetylation of a-terpineol or mixed isomeric terpineols (Bedoukian, 1967). |
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Synthesis Reference(s) |
Tetrahedron, 38, p. 1843, 1982 DOI: 10.1016/0040-4020(82)80261-5 |
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General Description |
Α-Terpinyl acetate, a monoterpene ester, is a commercially important fragrance molecule. It can be prepared from α-pinene in the presence of H-beta zeolite catalysts. The essential oils obtained from Stachys setifera ssp. iranica, Chamaecyparis obtuse leaves and Thymus willkomii contain Α-terpinyl acetate as one of the main components. |
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Flammability and Explosibility |
Nonflammable |
InChI:InChI=1/C12H20O2/c1-9(2)12(14-11(4)13)7-5-10(3)6-8-12/h5,7,9-10H,6,8H2,1-4H3
Pd-catalyzed oxidative coupling of camph...
We report the use of five alpha-hydroxy ...
The preparation of α-terpineol by direct...
The purpose of this study is to determin...
A series of novel α-terpineol derivative...
nitrosyl acetate
2αH-pinan-3α-ylamine
terpineol
1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate
terpinyl acetate
pinan-2α-ol
isobornyl acetate
limonene.
| Conditions | Yield |
|---|---|
|
In
acetic acid;
at 25 ℃;
|
12 % Chromat. 13 % Chromat. 12 % Chromat. 34 % Chromat. 4 % Chromat. 4 % Chromat. |
acetic acid
limonene.
carvyl acetate
terpinyl acetate
| Conditions | Yield |
|---|---|
|
With
lithium nitrate; oxygen; palladium diacetate;
at 60 ℃;
for 4h;
under 750.075 Torr;
|
1,8-Cineole
acetic anhydride
terpineol
sodium acetate
Terpinolene
4-methylisopropylbenzene
trans-sobrerol
endo-4-methyl-7,7-dimethyl-6-thiabicyclo<3.2.1>octane
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