24909-68-0

Basic information

• Product Name: LINOLEIC ANHYDRIDE
• Synonyms: LINOLEIC ANHYDRIDE;CIS,CIS-9,12-OCTADECADIENOIC ANHYDRIDE;12-octadecadienoicacid(z,z)-anhydride;Bis[(9Z,12Z)-9,12-octadecadienoic]anhydride;9,12-Octadecadienoic acid (9Z,12Z)-, 1,1'-anhydride;9,12-Octadecadienoic acid (9Z,12Z)-, anhydride;Linoleic acid anhydride
• CAS NO: 24909-68-0
• Molecular Formula: C₃₆H₆₂O₃
• Molecular Weight: 542.88
• Mol File: 24909-68-0.mol

Chemical Properties

• Melting Point: -3--1 °C
• Boiling Point: 607.7°Cat760mmHg
• Flash Point: 275.3°C
• Appearance: /
• Density: 0.90
• Vapor Pressure: 1.03E-14mmHg at 25°C
• Refractive Index: 1.4740 to 1.4780
• Storage Temp.: Refrigerator
• CAS DataBase Reference: LINOLEIC ANHYDRIDE(CAS DataBase Reference)
• NIST Chemistry Reference: LINOLEIC ANHYDRIDE(24909-68-0)
• EPA Substance Registry System: LINOLEIC ANHYDRIDE(24909-68-0)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-27-36/37/39-45
• Hazardous Substances Data: 24909-68-0(Hazardous Substances Data)

Usage

Uses

Used in the Coatings Industry:
Linoleic anhydride is utilized as a key ingredient in the formulation of coatings, enhancing their performance and durability. Its reactivity allows for the creation of compounds with unique functional properties, making it suitable for applications in the automotive, construction, and packaging sectors.
Used in the Adhesives Industry:
As a versatile component, linoleic anhydride is employed in the production of adhesives, where it contributes to the development of strong bonds between different materials. Its ability to participate in various chemical reactions ensures the creation of adhesives with improved properties, suitable for a wide range of applications.
Used in the Plasticizers Industry:
Linoleic anhydride is also used as a component in the manufacturing of plasticizers, which are additives that increase the flexibility and workability of plastics. Its incorporation into plasticizers can lead to the production of materials with enhanced properties, catering to specific industrial needs.

InChI:InChI=1/C36H62O3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35(37)39-36(38)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h11-14,17-20H,3-10,15-16,21-34H2,1-2H3/b13-11-,14-12-,19-17-,20-18-

Upstream product

• 60-33-3 linoleic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 2442-53-7 1-octadeca-9,12-dienoyloxy-2,3-bis-stearoyloxy-propane 
• 2535-35-5 1,2-Bis-palmitoyloxy-3-linoleoyloxy-propan 
• 6753-53-3 1-octadecanoyl-2-[cis-9,12]-octadecadienoyl-glycero-3-phosphocholine 
• 1338939-12-0 2,4-diisopropylphenol linoleic acid 

Relevant articles and documents

Eco-friendly microwave-assisted protocol to prepare hyaluronan-fatty acid conjugates and to induce their self-assembly process

An environmentally sustainable and energy-efficient synthetic process has been developed to prepare hyaluronan-based nano-sized material. It consists in a microwave-promoted acylation of the hydroxyl function of the polysaccharide with natural fatty acids, performed under solvent-free conditions. The efficient interaction of the solid reagents with the MW radiation accounts for the obtained high yielded products. The self-assembly process of the obtained compounds very fast occurred in an aqueous medium under MW-radiation, thus allowing the development of a green protocol for the nano-particles preparation.

NOVEL CATIONIC LIPID EXHIBITING IMPROVED INTRACELLULAR DYNAMICS

The invention provides a cationic lipid, a lipid membrane structure containing same, and use thereof. The cationic lipid is represented by the formula (1) wherein R1a, R1b, R2a, R2b, R3a, R3b, Xa, Xb, Ya, Yb, Za, and Zb are as defined in the specification.

Synthesis and characterization of novel PUFA esters exhibiting potential anticancer activities: An in vitro study

Polyunsaturated fatty acids (PUFAs) have been reported to play a regulatory role in tumour growth progression. In the present study, we have synthesized ester derivatives of two important PUFA viz., linoleic acid (LA) and arachidonic acid (AA) with propof