Isopulegol acetate

Base Information

Chemical Name:Isopulegol acetate
CAS No.:89-49-6
Molecular Formula:C12H20O2
Molecular Weight:196.29
Hs Code.:
European Community (EC) Number:260-820-1
DSSTox Substance ID:DTXSID60861679
Nikkaji Number:J22.835D
Wikidata:Q105030157
Mol file:89-49-6.mol

Synonyms:isopulegyl acetate

Suppliers and Price of Isopulegol acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
ISOPULEGYL ACETATE 95.00%
100G
$ 2478.38

Total 13 raw suppliers

Chemical Property of Isopulegol acetate

Chemical Property:

Vapor Pressure:0.0248mmHg at 25°C
Refractive Index:n20/D 1.456(lit.)
Boiling Point:248 °C at 760 mmHg
Flash Point:85.6 °C
PSA：26.30000
Density:0.94g/cm³
LogP:2.93040
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:196.146329876
Heavy Atom Count:14
Complexity:233

Purity/Quality:

99% ^*data from raw suppliers

ISOPULEGYL ACETATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC(C(C1)OC(=O)C)C(=C)C
Description Isopulegyl acetate has a sweet, mint-like odor. Isopulegyl acetate may be synthesized by prolonged heating of citronellal with acetic anhydride (with or without sodium acetate).

Technology Process of Isopulegol acetate

There total 20 articles about Isopulegol acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

: 108-24-7
acetic anhydride

: 89-79-2,7786-67-6,18674-65-2,20549-46-6,21290-09-5,29141-10-4,50373-36-9,59905-53-2,59905-54-3,96612-21-4,104870-56-6,121468-66-4,122517-60-6,122517-61-7,144541-38-8
isopulegol

: 89-49-6,57576-09-7,57576-10-0,109010-10-8,109010-11-9,109010-12-0,109430-47-9
Acetic acid (1R,2S,5R)-2-isopropenyl-5-methyl-cyclohexyl ester

Guidance literature:: With pyridine; In benzene; for 36h; Ambient temperature;
DOI:10.1016/S0040-4020(01)85916-0

Reference yield:

: 503-74-2
3-methylbutyric acid

: 123-35-3
7-methyl-3-methene-1,6-octadiene

: 64-19-7,77671-22-8
acetic acid

: 141-12-8,8022-83-1
neryl acetate

: 105-87-3,8022-83-1
3,7-dimethyl-2E,6-octadien-1-yl acetate

: 3915-83-1
neryl 3-methylbutanoate

: 109-20-6
[(2E)-3,7-dimethylocta-2,6-dienyl] 3-methylbutanoate

: 89-49-6
Isopulegol acetate

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

Guidance literature:: With sodium acetate; In methoxybenzene; for 18h; under 760.051 Torr; Product distribution / selectivity; Heating / reflux;

Reference yield:

: 123-35-3
7-methyl-3-methene-1,6-octadiene

: 64-19-7,77671-22-8
acetic acid

: 141-12-8,8022-83-1
neryl acetate

: 105-87-3,8022-83-1
3,7-dimethyl-2E,6-octadien-1-yl acetate

: 89-49-6
Isopulegol acetate

Guidance literature:: With sodium acetate; In chlorobenzene; for 20 - 40h; under 760.051 Torr; Product distribution / selectivity; Heating / reflux;