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118101-31-8

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118101-31-8 Usage

General Description

(S,S)-(+)-1,2-Cyclo-dodecanediol is a chemical compound with the molecular formula C12H24O2. It is a white, waxy solid with a melting point of 58-60°C. (S,S)-(+)-1,2-CYCLODODECANEDIOL is also known as Dodecanediol, and it is used as a monomer in the production of thermoplastic polyurethane elastomers. It can also be used as a crosslinking agent in the preparation of epoxy resins. Additionally, (S,S)-(+)-1,2-Cyclo-dodecanediol has potential applications in the fields of pharmaceuticals, agrochemicals, and as a fragrance ingredient due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 118101-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,1,0 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118101-31:
(8*1)+(7*1)+(6*8)+(5*1)+(4*0)+(3*1)+(2*3)+(1*1)=78
78 % 10 = 8
So 118101-31-8 is a valid CAS Registry Number.

118101-31-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S,S)-(+)-1,2-CYCLODODECANEDIOL

1.2 Other means of identification

Product number -
Other names trans-Cyclododecan-1,2-diol

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:118101-31-8 SDS

118101-31-8Relevant articles and documents

Formation of persulphate from sodium sulphite and molecular oxygen catalysed by H5PV2Mo10O40-aerobic epoxidation and hydrolysis

Rubinstein, Amir,Carmeli, Raanan,Neumann, Ronny

, p. 13247 - 13249 (2015/05/20)

The H5PV2Mo10O40 polyoxometalate catalysed the electron transfer oxidation of sulphite to yield a sulphite radical, SO3- that upon addition of O2 yielded a peroxosulphate species efficient for the H5PV2Mo10O40 catalysed epoxidation of alkenes. The acidic polyoxometalate further catalysed hydrolysis of the epoxide to give vicinal diols in high yields. This journal is

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