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10235-63-9

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10235-63-9 Usage

Uses

γ-Terpinyl Acetate is used in the antiperspirant and deodorant compositions.

Check Digit Verification of cas no

The CAS Registry Mumber 10235-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,3 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10235-63:
(7*1)+(6*0)+(5*2)+(4*3)+(3*5)+(2*6)+(1*3)=59
59 % 10 = 9
So 10235-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-9(2)11-5-7-12(4,8-6-11)14-10(3)13/h5-8H2,1-4H3

10235-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-methyl-4-propan-2-ylidenecyclohexyl) acetate

1.2 Other means of identification

Product number -
Other names Essigsaeure-p-menth-4(8)-en-1-ylester

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:10235-63-9 SDS

10235-63-9Relevant articles and documents

A NOVEL METHOD OF SYNTHESIZING TRANS-β-TERPINYL ESTERS FROM TRANS-TERPIN-1,8

Kaminska, Janina,Gora, Jozef

, p. 757 - 765 (2007/10/02)

A novel method of synthesizing trans-β-terpinyl esters based on selective elimination of one mole of carboxylic acid from trans-terpin-1,8 diesters with aliphatic acids C2 to C5 and benzoic acid has been described.Elimination reaction was carried out at temperature 120-190 deg C in media of acid anhydrides, in presence of sodium salt of the same acid.Terpinyl esters were obtained in 30-75percent yield.Selectivity of elimination has increased with increase in molecular weight of eliminated acid from 81percent for acetic to 94percent for n-pentanoic, and 95percent for benzoic.

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