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2050-61-5

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2050-61-5 Usage

General Description

Bis(2-methylpropyl) oxalate is a colorless liquid chemical compound with the molecular formula C14H26O4. It is commonly used as a solvent in the production of various chemicals and as a plasticizer in the manufacturing of plastics and polymers. Bis(2-methylpropyl) oxalate is also used in the synthesis of pharmaceuticals, dyes, and other organic compounds. It has a low volatility and high boiling point, making it suitable for applications requiring a stable and non-volatile solvent. However, it should be handled with caution as it is flammable and may cause irritation to the skin and eyes upon contact. Overall, bis(2-methylpropyl) oxalate is a versatile chemical with a variety of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2050-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2050-61:
(6*2)+(5*0)+(4*5)+(3*0)+(2*6)+(1*1)=45
45 % 10 = 5
So 2050-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O4/c1-7(2)5-13-9(11)10(12)14-6-8(3)4/h7-8H,5-6H2,1-4H3

2050-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(2-methylpropyl) oxalate

1.2 Other means of identification

Product number -
Other names oxalic acid diisobutyl ester

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:2050-61-5 SDS

2050-61-5Relevant articles and documents

Process for preparing diesters of dicarboxylic acids

-

, (2008/06/13)

A process for preparing a diester of a dicarboxylic acid having two more carbon atoms than the unsaturated hydrocarbon used as the starting material, which comprises subjecting an unsaturated hydrocarbon, carbon monoxide and an alcohol to reaction in the presence of a platinum group metal or a salt thereof; a compound selected from the group consisting of nitric acid, a nitrogen oxide and an ester of nitrous acid; and a halogen compound.

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