71340-46-0

Usage

Uses

Used in Personal Care and Food Industry:
Diisopropyl glutarate is used as a fragrance and flavoring agent for its fruity scent and ability to enhance the sensory experience of personal care products and food items.
Used in Industrial Applications:
Diisopropyl glutarate is used as a solvent in the formulation of coatings, paints, and adhesives, thanks to its compatibility with various substances and quick evaporation properties.
Used as a Plasticizer:
Diisopropyl glutarate is used as a plasticizer to improve the flexibility and durability of plastics and polymers, contributing to the enhanced performance and longevity of these materials.

InChI:InChI=1/C11H20O4/c1-8(2)14-10(12)6-5-7-11(13)15-9(3)4/h8-9H,5-7H2,1-4H3

Upstream product

• 201230-82-2 carbon monoxide 
• 107-18-6 allyl alcohol 
• 67-63-0 isopropyl alcohol 
• 1193-55-1 2-methylcyclohexane-1,3-dione 

Relevant academic research and scientific papers

PROCESS FOR DOUBLE CARBONYLATION OF ALLYL ALCOHOLS TO CORRESPONDING DIESTERS

The invention relates to a process for doubly carbonylating allyl alcohols to the corresponding diesters, wherein a linear or branched allyl alcohol is reacted with a linear or branched alkanol (alcohol) with supply of CO and in the presence of a catalytic system composed of a palladium complex and at least one organic phosphorus ligand and in the presence of a hydrogen halide selected from HCl, HBr and HI.

CYCLOHEXANE OXIDATION PROCESS BYPRODUCT DERIVATIVES AND METHODS FOR USING THE SAME

Disclosed are ester compositions, solvents, cleaning formulations, curing agents, reactive diluent solvents, controlled acid function release agents, polyol monomers, drilling mud and methods of making and using the same. Disclosed compositions include: a) about 10 to 60 weight percent methyl hydroxycaproate; b) about 20 to 80 weight percent dimethyl adipate; c) about 1 to 15 wt % of dimethyl glutarate; d) about 0.1 to 5 wt % of dimethyl succinate; e) about 0.1 to 7 wt % of at least one cyclohexanediol; and f) less than about 20 wt% oligomeric esters.

Direct oxidative cleavage of α- and β-dicarbonyls and α-hydroxyketones to diesters with KHSO5

Presented is a methodology to oxidatively cleave α-hydroxyketones and α- or β-diones using the environmentally benign reagent KHSO 5, prepared easily from Oxone, to diesters in one simple transformation. In addition, we undertook a mechanistic study to provide a plausible mechanistic interpretation. These reactions may prove to be valuable alternatives to other related metal-mediated processes.