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110-33-8

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110-33-8 Usage

General Description

Dihexyl adipate is a chemical compound that belongs to a class of organic compounds known as carboxylic esters. It is used commonly as a plasticizer, a substance added to materials to augment their qualities such as flexibility, durability, pliability, or longevity. This chemical is synthesized by the esterification of adipic acid with hexanol. It is mostly utilized in the plastic and polymer industry, particularly in PVC products. Additionally, it features in cosmetics due to its moisturizing and softening properties. Dihexyl adipate is odorless, possesses a relatively high boiling point, and is resistant to cold temperatures.

Check Digit Verification of cas no

The CAS Registry Mumber 110-33-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110-33:
(5*1)+(4*1)+(3*0)+(2*3)+(1*3)=18
18 % 10 = 8
So 110-33-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O4/c1-3-5-7-11-15-21-17(19)13-9-10-14-18(20)22-16-12-8-6-4-2/h3-16H2,1-2H3

110-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dihexyl hexanedioate

1.2 Other means of identification

Product number -
Other names EINECS 203-757-7

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:110-33-8 SDS

110-33-8Synthetic route

Adipic acid
124-04-9

Adipic acid

hexan-1-ol
111-27-3

hexan-1-ol

dihexyl adipate
110-33-8

dihexyl adipate

Conditions
ConditionsYield
With Fe(SO4)3 * xH2O for 1h; Heating;95%
With pyrographite; toluene-4-sulfonic acid for 0.0111111h; Esterification; Ring cleavage; Microwave irradiation (600 W);92%
With toluene-4-sulfonic acid; xylene
at 150 - 155℃;
With [AlMo6]Anderson-type heteropolyacid at 120℃; for 12h;
carbon monoxide
201230-82-2

carbon monoxide

buta-1,3-diene
106-99-0

buta-1,3-diene

hexan-1-ol
111-27-3

hexan-1-ol

dihexyl adipate
110-33-8

dihexyl adipate

Conditions
ConditionsYield
With palladium(II) trifluoroacetate; toluene-4-sulfonic acid; 1,2-bis[di(t-butyl)phosphinomethyl]benzene In toluene at 120℃; under 30003 Torr; for 24h; Autoclave; Green chemistry; regioselective reaction;73%
With palladium(II) trifluoroacetate; HeMaRaphos; toluene-4-sulfonic acid In toluene at 120℃; under 30003 Torr; for 24h; regioselective reaction;83 %Chromat.
Adipic acid
124-04-9

Adipic acid

dihexyl phosphonate
6151-90-2

dihexyl phosphonate

dihexyl adipate
110-33-8

dihexyl adipate

Conditions
ConditionsYield
at 178℃;
Adipic acid dichloride
111-50-2

Adipic acid dichloride

hexan-1-ol
111-27-3

hexan-1-ol

dihexyl adipate
110-33-8

dihexyl adipate

Adipic acid
124-04-9

Adipic acid

hexan-1-ol
111-27-3

hexan-1-ol

A

dihexyl adipate
110-33-8

dihexyl adipate

B

Adipinsaeure-monohexylester
17961-14-7

Adipinsaeure-monohexylester

Conditions
ConditionsYield
With Candida antarctica lipase immobilized on polyacrylic resin In 1,4-dioxane for 3h; microwave irradiation; Title compound not separated from byproducts;

110-33-8Downstream Products

110-33-8Relevant articles and documents

Efficient Palladium-Catalyzed Carbonylation of 1,3-Dienes: Selective Synthesis of Adipates and Other Aliphatic Diesters

Yang, Ji,Liu, Jiawang,Ge, Yao,Huang, Weiheng,Ferretti, Francesco,Neumann, Helfried,Jiao, Haijun,Franke, Robert,Jackstell, Ralf,Beller, Matthias

supporting information, p. 9527 - 9533 (2021/03/08)

The dicarbonylation of 1,3-butadiene to adipic acid derivatives offers the potential for a more cost-efficient and environmentally benign industrial process. However, the complex reaction network of regioisomeric carbonylation and isomerization pathways, make a selective and direct transformation particularly difficult. Here, we report surprising solvent effects on this palladium-catalysed process in the presence of 1,2-bis-di-tert-butylphosphin-oxylene (dtbpx) ligands, which allow adipate diester formation from 1,3-butadiene, carbon monoxide, and methanol with 97 % selectivity and 100 % atom-economy under scalable conditions. Under optimal conditions a variety of di- and triesters from 1,2- and 1,3-dienes can be obtained in good to excellent yields.

Direct synthesis of adipic acid esters via palladium-catalyzed carbonylation of 1,3-dienes

Yang, Ji,Liu, Jiawang,Neumann, Helfried,Franke, Robert,Jackstell, Ralf,Beller, Matthias

, p. 1514 - 1517 (2020/01/08)

The direct carbonylation of 1,3-butadiene offers the potential for a more cost-efficient and environmentally benign route to industrially important adipic acid derivatives. However, owing to the complex reaction network of regioisomeric carbonylation and isomerization pathways, a selective practical catalyst for this process has thus far proven elusive. Here, we report the design of a pyridyl-substituted bidentate phosphine ligand (HeMaRaphos) that, upon coordination to palladium, catalyzes adipate diester formation from 1,3-butadiene, carbon monoxide, and butanol with 97% selectivity and 100% atom-economy under industrially viable and scalable conditions (turnover number > 60,000). This catalyst system also affords access to a variety of other di- and triesters from 1,2- and 1,3-dienes.

Esterification by microwave irradiation on activated carbon

Fan, Xingjun,Yuan, Keguo,Hao, Caili,Li, Nan,Tan, Ganzu,Yu, Xianda

, p. 287 - 290 (2007/10/03)

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