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Diheptyl succinate is a chemical compound formed by the esterification of two molecules of caprylic acid with succinic acid, resulting in a diester. It is recognized for its plasticizing and conditioning properties, making it a versatile substance in various industrial applications.

15872-89-6

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15872-89-6 Usage

Uses

Used in Plastics Industry:
Diheptyl succinate is used as a plasticizer for [improving flexibility, durability, and resistance to heat and chemicals] in the production of polyvinyl chloride (PVC) and other polymers. It enhances the physical properties of these materials, offering a safer alternative to traditional phthalate-based plasticizers due to its biodegradability and lower toxicity.
Used in Cosmetics and Personal Care Industry:
Diheptyl succinate is used as an emollient and skin conditioning agent for [providing skin softening and moisturizing effects] in cosmetics and personal care products. Its conditioning properties contribute to the product's efficacy in maintaining skin health and comfort.

Check Digit Verification of cas no

The CAS Registry Mumber 15872-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15872-89:
(7*1)+(6*5)+(5*8)+(4*7)+(3*2)+(2*8)+(1*9)=136
136 % 10 = 6
So 15872-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O4/c1-3-5-7-9-11-15-21-17(19)13-14-18(20)22-16-12-10-8-6-4-2/h3-16H2,1-2H3

15872-89-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name diheptyl butanedioate

1.2 Other means of identification

Product number -
Other names succinic acid diheptyl 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:15872-89-6 SDS

15872-89-6Downstream Products

15872-89-6Relevant academic research and scientific papers

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

Chen, Zhe,Han, Sheng,Lu, Deli,Xu, Yumeng

, (2021/08/23)

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.

By using low-temperature co- melt solvent a method of catalytic ester (by machine translation)

-

Paragraph 0054; 0055, (2017/01/17)

The invention discloses a method of utilizing low-temperature co- melt solvent catalytic ester method, will be 0.05-0.5 mole of sharemelt solvent of low-temperature co-preprocessing, 1-5 mole of share alcohol and 1-10 mole of share of acid in the reaction vessel, stirring and heating, 25-200 ° C reaction under 2-96h, then the reaction fluid settlement , liquid, organic is accepted after passing an examination the level , get the esterification reaction products of the; reaction after the treatment and recovery of low-temperature co- melt solvent the preprocessing, can be reused. This invention utilizes the easy preparation of low-temperature co- melt solvent the preprocessing of catalytic esterification reaction, the reaction front is homogeneous, can be formed after the reaction of the two-phase reaction in the process of direct dehydration, without adding other dehydrating agent, has the advantages of simple operation, the reaction efficiency is high, corrosion of small equipment, less side reactions, the product quality is good, no pollution to the environment, and the like, it has broad application prospects. (by machine translation)

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