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141-03-7

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141-03-7 Usage

Chemical Properties

It is a mobile liquid that is soluble in alcohol, benzene, and ether, but insoluble in water. Its melting and boiling points are -29 and 274.5°C, respectively. The flash point is 275°F.

Uses

Different sources of media describe the Uses of 141-03-7 differently. You can refer to the following data:
1. Dibutyl succinate is a diester compound for proteomics research.
2. Dibutyl succinate especially against biting flies of cattle, household ants and roaches.

Check Digit Verification of cas no

The CAS Registry Mumber 141-03-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141-03:
(5*1)+(4*4)+(3*1)+(2*0)+(1*3)=27
27 % 10 = 7
So 141-03-7 is a valid CAS Registry Number.

141-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl succinate

1.2 Other means of identification

Product number -
Other names Succinic Acid di-n-Butyl Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:141-03-7 SDS

141-03-7Relevant articles and documents

CARBALKOXYLATION OF ACETYLENE IN SOLUTIONS OF MOLYBDENUM AND TUNGSTEN COMPLEXES

Bruk, L. G.,Boldyreva, L. B.,Zakharova, L. A.,Ustynyuk, N. A.,Belyi, A. A.,Shestakov, G. K.

, p. 207 - 209 (1983)

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Biobased compositions

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Page/Page column 14-15, (2021/08/05)

A composition comprised of a component selected from the group consisting of a biobased bis-alkyl succinate and a biobased bis-alkyl sebacate, each derived, for example, from the esterification of biobased diacid such as succinic acid or sebacic acid, and a biobased alcohol and a biobased polyester.

Method for preparing succinate by double carbonylation of acetylene

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Paragraph 0027-0038, (2019/12/02)

The invention provides a method for preparing succinate by double carbonylation of acetylene. Acetylene, carbon monoxide and an alcohol compound are used as raw materials and subjected to the double carbonylation reaction in a solvent under the catalysis of a catalyst, and the succinate compound is obtained. The catalyst is composed of a palladium compound, a lithium halide/acid auxiliary agent and a nitrogen-oxygen ligand, wherein the nitrogen-oxygen ligand is one or more of 2-hydroxypyridine, 3-hydroxypyridine and 2-picolinic acid, and the dosage of the catalyst is 0.0001-1.0% of the total weight of the reaction system; in the reaction system, the molar ratio of acetylene to the alcohol compound is 1:(2-16), and the molar ratio of the alcohol compound to the solvent is 1:(7-35). According to the method, the succinate compounds can be produced by a one-pot method, wherein the process is simple, and the investment cost of an industrial device is low; the reaction conditions in the production process are mild, the catalytic activity of the catalyst is high, the stability is high, the service life is long, the yield can reach 90% or above, and the higher technical competitive advantage is achieved.

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