105-80-6

Basic information

• Product Name: Nonanedioic acid,1,9-bis(2-methylpropyl) ester
• Synonyms: Azelaicacid, diisobutyl ester (7CI,8CI); Nonanedioic acid, bis(2-methylpropyl) ester(9CI); Diisobutyl azelate; Hallco 3880
• CAS NO: 105-80-6
• Molecular Formula: C₁₇H₃₂O₄
• Molecular Weight: 300.4336
• EINECS: 203-333-1
• Mol File: 105-80-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 321.3°Cat760mmHg
• Flash Point: 140.9°C
• Appearance: /
• Density: 0.948g/cm³
• Vapor Pressure: 0.0003mmHg at 25°C
• Refractive Index: 1.444
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Nonanedioic acid,1,9-bis(2-methylpropyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Nonanedioic acid,1,9-bis(2-methylpropyl) ester(105-80-6)
• EPA Substance Registry System: Nonanedioic acid,1,9-bis(2-methylpropyl) ester(105-80-6)

Safety Data

• Hazardous Substances Data: 105-80-6(Hazardous Substances Data)

Usage

General Description

Nonanedioic acid, 1,9-bis(2-methylpropyl) ester is a chemical compound that is commonly used as a plasticizer and lubricant in various industrial applications. It is a colorless liquid with a slight odor and is soluble in organic solvents. Nonanedioic acid,1,9-bis(2-methylpropyl) ester is known for its ability to improve the flexibility and durability of plastics and rubbers, making it a valuable ingredient in the manufacturing of PVC products, such as wires and cables, automotive parts, and medical devices. It is also used in the production of adhesives, sealants, and coatings. However, it is important to handle this chemical with care as it may be harmful if swallowed, inhaled, or comes into contact with the skin and eyes.

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

Relevant articles and documents

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

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.