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20405-60-1

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20405-60-1 Usage

General Description

(+)-dihydrocarvyl acetate, mixture of isomers is a chemical compound that is a combination of different isomers of the same compound. It is primarily used as a flavor and fragrance ingredient, providing a fresh, minty, and slightly citrusy aroma. This chemical is commonly found in various cosmetic and personal care products, as well as in food and beverage products. It is also used in the production of perfumes, soaps, and other scented products. The compound has been shown to have low toxicity and is generally considered safe for use in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 20405-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,0 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20405-60:
(7*2)+(6*0)+(5*4)+(4*0)+(3*5)+(2*6)+(1*0)=61
61 % 10 = 1
So 20405-60-1 is a valid CAS Registry Number.

20405-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dihydro carvyl acetate

1.2 Other means of identification

Product number -
Other names (+)-DIHYDROCARVYL ACETATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:20405-60-1 SDS

20405-60-1Relevant articles and documents

OXIDATIVE SUBSTITUTION REACTION OF OLEFINIC TIN COMPOUNDS WITH LEAD TETRAACETATE

Yamamoto, Makoto,Irie, Shin,Miyashita, Michio,Kohmoto, Shigeo,Yamada, Kazutoshi

, p. 221 - 222 (2007/10/02)

The oxidative substitution reaction of olefinic tin compounds with lead tetraacetate(LTA) was investigated.The oxidation is highly regioselective and gave a dipole inversed product (acetate) in good yield.

A NEW METHOD FOR CLEAVING METHYL AND METHYLTHIOMETHYL ETHERS

Barua, Nabin C.,Sharma, Ram P.,Baruah, Jogendra N.

, p. 1189 - 1190 (2007/10/02)

Chlorotrimethylsilane (CTMS) and acetic anhydride has been shown to cleave methyl and methylthiomethyl ethers to furnish the corresponding acetates in excellent yield.Tertiary alcohols can be acetylated efficiently with this reagent combination.

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