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(S)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is a complex acetate ester chemical compound derived from acetic acid and an alcohol. It features a cyclohexene ring with three methyl groups and an additional methyl group attached to the carbon next to the double bond. This unique molecular structure endows it with valuable chemical properties that make it suitable for a variety of applications.

58206-95-4

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58206-95-4 Usage

Uses

Used in Flavor and Fragrance Industry:
(S)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is used as an additive in the flavor and fragrance industry for its ability to enhance the aroma and taste of various products. Its unique chemical structure contributes to the creation of distinct and appealing scents and flavors.
Used in Cosmetics Industry:
In the cosmetics industry, (S)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is used as a component in the formulation of various cosmetic products. Its chemical properties help improve the product's performance, stability, and sensory characteristics, making it an essential ingredient in the development of high-quality cosmetics.
Used as a Solvent:
(S)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is utilized as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a versatile and effective medium for carrying out chemical reactions and separations.
Used in Chemical Production:
(S)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is also used in the production of other chemicals, where its unique structure and properties are harnessed to synthesize new and useful materials. Its role in chemical production is crucial for the development of innovative products and technologies across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 58206-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58206-95:
(7*5)+(6*8)+(5*2)+(4*0)+(3*6)+(2*9)+(1*5)=134
134 % 10 = 4
So 58206-95-4 is a valid CAS Registry Number.

58206-95-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-(-)-α-terpinyl acetate

1.2 Other means of identification

Product number -
Other names α-terpinenyl acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58206-95-4 SDS

58206-95-4Relevant academic research and scientific papers

Heteropoly acid catalysts for the synthesis of fragrance compounds from bio-renewables: Acetylation of nopol and terpenic alcohols

Costa, Vinicius V.,Da Silva Rocha, Kelly A.,Oliveira, Luiz C. A.,Kozhevnikova, Elena F.,Kozhevnikov, Ivan V.,Gusevskaya, Elena V.

, p. 43217 - 43222 (2016/05/24)

The cesium salt of tungstophosphoric heteropoly acid, Cs2.5H0.5PW12O40, is an active and environmentally friendly heterogeneous catalyst for the liquid-phase acetylation of nopol and several biomass-derived terpenic alcohols (i.e., α-terpineol, nerol, geraniol, linalool, menthol, isoborneol, perillyl alcohol, carveol, isopulegol, carvacrol and nerolidol) with acetic anhydride. The resulting flavor and fragrance acetic esters, which are widely used in perfumery, household and food products, are obtained in good to excellent yields. The reactions occur at room temperature with low catalyst loadings without substantial catalyst leaching and can be performed with stoichiometric amounts of an acetylating agent in solvent free systems.

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