Terpinyl Acetate

Available forms:clear liquid

pd_proNo:383907-839c91d9-25ae-44db-8896-a8992a2722cf

pd_productuse:

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Detailed introduction

Cost-effective customized wholesale Terpinyl Acetate 80-26-2

  • Molecular Formula:C12H20O2
  • Molecular Weight:196.29
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:3.515Pa at 23℃ 
  • Melting Point:112-113.5 °C 
  • Refractive Index:1.464 - 1.473 
  • Boiling Point:239.872 °C at 760 mmHg 
  • Flash Point:82.974 °C 
  • PSA:26.30000 
  • Density:0.962 g/cm3 
  • LogP:3.07450 

Terpinyl acetate(Cas 80-26-2) Usage

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.

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).

Synthesis Reference(s)

Tetrahedron, 38, p. 1843, 1982 DOI: 10.1016/0040-4020(82)80261-5

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.

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

80-26-2 Relevant articles

Pd(OAc)2/M(NO3)n (M = Cu(II), Fe(III); n = 2, 3): Kinetic investigations of an alternative Wacker system for the oxidation of natural olefins

da Silva, Márcio J.,Teixeira, Róbson Ricardo,Carari, Danielli Marcolan

, p. 3254 - 3261 (2009)

Pd-catalyzed oxidative coupling of camph...

Synthesis of Terpineol from Alpha-Pinene Catalyzed by α-Hydroxy Acids

Hu, Yi-Ming,Huang, Xiao-Rui,Meng, Zhong-Lei,Qin, Rong-Xiu,Wen, Ru-Si,Zhou, Yong-Hong

, (2022/02/17)

We report the use of five alpha-hydroxy ...

Preparation of α-terpineol and perillyl alcohol using zeolites beta

?erveny, Libor,Vysko?ilová, Eli?ka,Zítová, Kate?ina

, p. 4297 - 4310 (2021/07/26)

The preparation of α-terpineol by direct...

Heterogeneous zeolite-based catalyst for esterification of α-pinene to α-terpinyl acetate

Wijayati, Nanik,Kusumastuti, Ella,Alighiri, Dante,Rohmawati, Baiti,Lusiana, Retno Ariadi

, p. 399 - 403 (2019/06/05)

The purpose of this study is to determin...

Discovery of a novel series of α-terpineol derivatives as promising anti-asthmatic agents: Their design, synthesis, and biological evaluation

Zhu, Wanping,Liu, Xia,Wang, Yuji,Tong, Yeling,Hu, Yongzhou

, p. 419 - 425 (2017/12/07)

A series of novel α-terpineol derivative...

80-26-2 Process route

nitrosyl acetate
5813-49-0

nitrosyl acetate

2αH-pinan-3α-ylamine
13293-47-5,17371-27-6,35117-55-6,35117-58-9,35117-61-4,35117-66-9,69460-11-3,69460-12-4,74281-72-4

2αH-pinan-3α-ylamine

terpineol
98-55-5,2438-12-2

terpineol

1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate
4057-31-2,13851-11-1,56282-46-3,69651-95-2,76109-40-5,99341-77-2,111821-74-0

1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate

terpinyl acetate
80-26-2

terpinyl acetate

pinan-2α-ol
473-54-1,4948-28-1,4948-29-2,18492-55-2,23516-36-1,25926-77-6,35408-04-9,35519-42-7,112574-21-7

pinan-2α-ol

isobornyl acetate
76-49-3,125-12-2,5655-61-8,6626-35-3,17283-45-3,20347-65-3,28974-17-6,36386-52-4,71424-71-0,92618-89-8

isobornyl acetate

limonene.
138-86-3,555-08-8,8022-90-0,9003-73-0,95327-98-3

limonene.

Conditions
Conditions Yield
In acetic acid; at 25 ℃;
12 % Chromat.
13 % Chromat.
12 % Chromat.
34 % Chromat.
4 % Chromat.
4 % Chromat.
acetic acid
64-19-7,77671-22-8

acetic acid

limonene.
138-86-3,555-08-8,8022-90-0,9003-73-0,95327-98-3

limonene.

carvyl acetate
97-42-7

carvyl acetate

terpinyl acetate
80-26-2

terpinyl acetate

Conditions
Conditions Yield
With lithium nitrate; oxygen; palladium diacetate; at 60 ℃; for 4h; under 750.075 Torr;

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