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Didecyl carbonate (DDC) is a colorless, oily liquid with the chemical formula C21H42O3. It is an organic compound that belongs to the class of carbonates, specifically alkyl carbonates. DDC is synthesized by the reaction of carbon monoxide and decanol in the presence of a catalyst, and it is widely used as a solvent, plasticizer, and intermediate in the production of various chemicals. It is also known for its low toxicity and biodegradability, making it a preferred substitute for more hazardous chemicals in certain applications. DDC is used in the manufacturing of polyurethane foams, lubricants, and as a component in the production of pharmaceuticals and agrochemicals. Its properties include a high boiling point, low volatility, and good solubility in organic solvents, which contribute to its utility in a range of industrial processes.

6290-55-7

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6290-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6290-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6290-55:
(6*6)+(5*2)+(4*9)+(3*0)+(2*5)+(1*5)=97
97 % 10 = 7
So 6290-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H42O3/c1-3-5-7-9-11-13-15-17-19-23-21(22)24-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3

6290-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name didecyl carbonate

1.2 Other means of identification

Product number -
Other names carbonic acid bis-decyl 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:6290-55-7 SDS

6290-55-7Downstream Products

6290-55-7Relevant articles and documents

The continuous acid-catalysed etherification of aliphatic alcohols using stoichiometric quantities of dialkyl carbonates

Parrott, Andrew J.,Bourne, Richard A.,Gooden, Peter N.,Poliakoff, Martyn,Irvine, Derek J.,Bevinakatti, Han. S.

supporting information; experimental part, p. 1420 - 1426 (2011/09/20)

A range of methyl and ethyl ethers of aliphatic alcohols have been synthesized cleanly in high yield by reacting the corresponding alcohol with dimethyl carbonate or diethyl carbonate over the solid acid catalyst, I-alumina. The reaction could be conducted at ambient pressure without the need for the large excess of dialkyl carbonate as previously reported in the literature. If the reaction was conducted at high pressure, the conversion of the starting alcohol was greatly reduced. However, high pressure CO2 can be used as the solvent without significant reduction in yield. This has implications for tandem reactions.

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