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Nonanedioic acid, 1,9-bis(2-methylpropyl) ester is a colorless liquid chemical compound with a slight odor, known for its solubility in organic solvents. It is widely recognized for its plasticizing and lubricating properties, which significantly enhance the flexibility and durability of plastics and rubbers.

105-80-6

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105-80-6 Usage

Uses

Used in Plastics and Rubber Industry:
Nonanedioic acid, 1,9-bis(2-methylpropyl) ester is used as a plasticizer and lubricant for improving the flexibility and durability of plastics and rubbers. It is particularly valuable in the manufacturing of PVC products such as wires and cables, automotive parts, and medical devices.
Used in Adhesives, Sealants, and Coatings Production:
This chemical compound is also utilized in the production of adhesives, sealants, and coatings, where its plasticizing properties contribute to the desired consistency and performance of these materials.
Safety Considerations:
It is crucial to handle Nonanedioic acid, 1,9-bis(2-methylpropyl) ester with care due to its potential harmful effects if swallowed, inhaled, or if it comes into contact with the skin and eyes. Proper safety measures should be implemented during its use in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 105-80-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105-80:
(5*1)+(4*0)+(3*5)+(2*8)+(1*0)=36
36 % 10 = 6
So 105-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H32O4/c1-14(2)12-20-16(18)10-8-6-5-7-9-11-17(19)21-13-15(3)4/h14-15H,5-13H2,1-4H3

105-80-6SDS

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 bis(2-methylpropyl) nonanedioate

1.2 Other means of identification

Product number -
Other names Azelaic 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:105-80-6 SDS

105-80-6Upstream product

105-80-6Downstream Products

105-80-6Relevant academic research and scientific papers

METHODS AND COMPOSITIONS INVOLVING ESTERS OF AZELAIC ACID AND OTHER DICARBOXYLIC ACIDS

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Page/Page column 19, (2008/06/13)

The present invention relates to formulations of azelaic acid esters and other dicarboxylic acid esters, and their derivatives. In preferred embodiments, the esters have the general Formula (I) wherein R1 and R2 are selected from hydrogen, alkyl groups of up to about 18 carbon atoms and aryl groups of up to about 18 carbon atoms and alkylene group of up to about 18 carbon atoms and an arylene group of up to about 18 carbon atoms. The alkyl, aryl, alkylene and aryl groups may be substituted or unsubstituted, branched or straight chains. In addition, R1 and R2 may contain heteroatoms and may be straight chained or branched, n is an integer from 1-16, and R1 and R2 are not simultaneously hydrogen. R2OOC-(CH2)n-COOR1 (I). The azelaic acid derivatives of Formula I of this invention are certain derivatives of azelaic acid and other alkyl geminal diacids which possess a desirable high lipophilicity and biphasic solubility in comparison to the parent compound, azelaic acid, and which are cleaved enzymatically to azelaic acid. Compounds produced from the compounds of Formula (I) by the enzymatic hydrolysis of the R1 and R2 groups are useful as anti-bacterial agents in mammals in vivo and have been contemplated to be used in the treatment of skin disease.

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