645-69-2

Usage

Uses

Used in Cosmetics and Personal Care Industry:
Dipentyl succinate is used as a fragrance ingredient and solvent for its pleasant scent and low volatility, enhancing the sensory experience of cosmetics and personal care products without evaporating quickly.
Used in Fragrance Industry:
In the fragrance industry, Dipentyl succinate serves as a fixative to help stabilize and prolong the scent of perfumes and other scented products, thanks to its low volatility.
Used in Food Industry:
Dipentyl succinate is utilized as a flavoring agent in food products, adding a pleasant taste and aroma while being considered safe for consumption.
Used in Industrial Applications:
As a lubricant, Dipentyl succinate reduces friction between surfaces in various mechanical applications, contributing to the smooth operation of machinery and equipment.
Dipentyl succinate is valued for its relatively safe profile, exhibiting low toxicity and minimal environmental impact, making it a preferred choice in multiple applications where safety and sustainability are concerns.

InChI:InChI=1/C14H26O4/c1-3-5-7-11-17-13(15)9-10-14(16)18-12-8-6-4-2/h3-12H2,1-2H3

Upstream product

• 71-41-0 pentan-1-ol 
• 110-15-6 succinic acid 
• 5411-55-2 n-pentyl 2-chloroacetate 
• 100-66-3 methoxybenzene 
• 543-20-4 succinoyl dichloride 

Relevant academic research and scientific papers

EFFECT OF CYCLODEXTRIN ON INTERMOLECULAR PHOTOALKOXYCARBONYLMETHYLATION OF ANISOLE

The photolyses of anisole (1) and pentyl chloroacetate (2b) in isotropic media produce both alkylation products 3b-5b and dipentyl succinate (6b).In α- and β-CD complexes in aqueous solutions, 6b was absent and the o-alkylation product 3b was predominant.A cage effect and geometric control are attributed to the observed selective product distribution in α- and β-CD complexes in aqueous solutions.

Biomass-derived dibasic acids to diesters with inorganic ligand-supported catalyst: synthesis, optimization, characterization

Several attempts have been made to obtain aliphatic dicarboxylic diesters from esterification reaction to develop the biomass-derived platform molecules and green manufacturing processes. In this paper, Na3(H2O)6[AlMo6O18(OH)6], an Anderson-type polyoxometalate, firstly, was reported as a catalyst for diester synthesis from dicarboxylic acid to diester which showed an well productivity and selectivity characterized by 1H and 13C. Response surface methodology (RSM) integrated with the desirability function approach was used to determine the best operative conditions, and the optimal reaction parameters for maximum dipropyl succinate yield (77 ± 2.5%) were identified as 1.19?mol.% catalyst loading, 4.9:1 propanol/succinic acid ratio, 113?°C, and 9.6?h. Three batches of tests were carried for catalyst recycling with 78–75% yield even after 6 cycles of esterification. In addition, the substrate carbon chain was increased for investigation of substrate scope achieving satisfactory results and all products were characterized by 1H and 13C nuclear magnetic resonance spectroscopy.

A Mild, Simple, and Convenient Synthesis of Diesters from Malonyl or Succinyl Dichloride and Alcohols Catalyzed by Potassium Tetracarbonylhydridoferrate, KHFe(CO)4, as a New Catalyst

A large variety of alcohols react with acyl halides of dicarboxylic acids such as malonyl dichloride and succinyl dichloride in the presence of a catalytic amount of tetracarbonylhydridoferrate at room temperature under carbon monoxide or nitrogen to give the corresponding diesters in good yields.