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344397-18-8

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344397-18-8 Usage

Physical state

colorless, viscous liquid

Type of compound

organic

Usage

production of plastics, textiles, and pharmaceuticals

Functional groups

contains two hydroxyl (OH) functional groups

Classification

diol

Versatility

versatile building block for various chemical processes

Additional uses

solvent, precursor for the synthesis of other organic compounds

Legal status

controlled substance in some countries due to potential misuse in the illegal production of gamma-hydroxybutyric acid (GHB)

Regulation

sale and use are regulated in many jurisdictions

Check Digit Verification of cas no

The CAS Registry Mumber 344397-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,3,9 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 344397-18:
(8*3)+(7*4)+(6*4)+(5*3)+(4*9)+(3*7)+(2*1)+(1*8)=158
158 % 10 = 8
So 344397-18-8 is a valid CAS Registry Number.

344397-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-butene-1,4-diol

1.2 Other means of identification

Product number -
Other names 1,4-BUTENEDIOL

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:344397-18-8 SDS

344397-18-8Relevant articles and documents

Process for separating an oxidation reaction product and an oxidation catalyst

-

, (2008/06/13)

An oxidation reaction mixture (e.g. adipic acid, benzoic acid, butenediol) and an oxidation catalyst are efficiently separated from a reaction mixture with the use of an aqueous solvent (e.g. methyl benzoate, benzonitrile) containing at least water (e.g. water) and a non-water-soluble solvent separable from the aqueous solvent, the reaction mixture being obtained by oxidizing a substrate (e.g. a hydrocarbon) in the presence of an imide compound such as N-hydroxyphthalimide shown by the following formula (1) as the oxidation catalyst, wherein R1and R2represents a substituent such as a hydrogen atom and a halogen atom; R1and R2may together form a double bond, or an aromatic or nonaromatic 5- to 12-membered ring; X stands for O or OH; and n is 1 to 3. No decomposition of the oxidation catalyst is observed in this separation process.

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