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103-23-1

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103-23-1 Usage

Chemical Properties

colourless oily liquid

Uses

Different sources of media describe the Uses of 103-23-1 differently. You can refer to the following data:
1. The compound is used as a plasticizer for flexible vinyl food wraps and as a solvent for aircraft lubricants.
2. Plasticizer in polyvinyl chloride films, sheeting, extrusions, and plastisols; solvent and emollient in cosmetics
3. Bis(2-ethylhexyl) adipate also known as dioctyl adipate (DOA) can be used as a plasticizer for improving the impact properties of polymers. DOA is also used to produce clear films for food packaging applications and in synthetic rubber industries due to its compatibility with nitrocellulose and ethylcellulose.

Definition

ChEBI: A diester resulting from the formal condensation of the carboxy groups of adipic acid with 2-ethylhexan-1-ol. It is used as a plasticiser in the preparation of various polymers.

Production Methods

DEHA is manufactured by esterification of adipic acid and 2-ethylhexanol.

General Description

Colorless to straw-colored liquid with a mild odor. Floats on water.

Air & Water Reactions

Bis(2-ethylhexyl) adipate slowly hydrolyzes. Insoluble in water.

Reactivity Profile

Bis(2-ethylhexyl) adipate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Can generate electrostatic charges. [Handling Chemicals Safely 1980. p. 250]. Bis(2-ethylhexyl) adipate is incompatible with oxidizing materials and water. Bis(2-ethylhexyl) adipate is also incompatible with nitrates.

Health Hazard

Liquid may cause mild eye irritation. Repeated or prolonged skin contact may cause irritation.

Fire Hazard

Behavior in Fire: Use water spray to cool exposed containers.

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by intravenous route. Mildly toxic by ingestion. Experimental reproductive effects. Mutation data reported. An eye and skin irritant. Questionable carcinogen with experimental carcinogenic data. See also ESTERS. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 103-23-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103-23:
(5*1)+(4*0)+(3*3)+(2*2)+(1*3)=21
21 % 10 = 1
So 103-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H42O4/c1-5-9-13-19(7-3)17-25-21(23)15-11-12-16-22(24)26-18-20(8-4)14-10-6-2/h19-20H,5-18H2,1-4H3/t19-,20+

103-23-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L10195)  Bis(2-ethylhexyl) adipate, 99%   

  • 103-23-1

  • 25g

  • 379.0CNY

  • Detail
  • Alfa Aesar

  • (L10195)  Bis(2-ethylhexyl) adipate, 99%   

  • 103-23-1

  • 100g

  • 726.0CNY

  • Detail
  • Supelco

  • (442492)  Bis(2-ethylhexyl)adipate  analytical standard

  • 103-23-1

  • 000000000000442492

  • 449.28CNY

  • Detail
  • Sigma-Aldrich

  • (02138)  Bis(2-ethylhexyl)adipate  Selectophore, ≥99.0%

  • 103-23-1

  • 02138-1ML

  • 304.20CNY

  • Detail
  • Sigma-Aldrich

  • (02138)  Bis(2-ethylhexyl)adipate  Selectophore, ≥99.0%

  • 103-23-1

  • 02138-5ML

  • 826.02CNY

  • Detail
  • Sigma-Aldrich

  • (02138)  Bis(2-ethylhexyl)adipate  Selectophore, ≥99.0%

  • 103-23-1

  • 02138-25ML

  • 2,880.54CNY

  • Detail
  • Aldrich

  • (525197)  Bis(2-ethylhexyl)adipate  99%

  • 103-23-1

  • 525197-5ML

  • 826.02CNY

  • Detail
  • Aldrich

  • (525197)  Bis(2-ethylhexyl)adipate  99%

  • 103-23-1

  • 525197-1L

  • 1,060.02CNY

  • Detail

103-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-ethylhexyl) adipate

1.2 Other means of identification

Product number -
Other names Bis(2-ethylhexyl)adipat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives,Plasticizers
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:103-23-1 SDS

103-23-1Synthetic route

Adipic acid
124-04-9

Adipic acid

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

Conditions
ConditionsYield
With triflic acid on silica-encapsulated superparamagnetic iron oxide nanoparticles In neat (no solvent) at 90℃; for 0.333333h; Catalytic behavior; Time; Reagent/catalyst; Flow reactor; Green chemistry;96%
In 5,5-dimethyl-1,3-cyclohexadiene at 160℃; for 2h;90%
With Candida antarctica lipase B In cyclohexane at 45℃; for 24h;66%
With sulfuric acid; benzene
Adipic acid
124-04-9

Adipic acid

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

A

di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

B

bis(1-hexyl-4-ethyloctyl) adipate

bis(1-hexyl-4-ethyloctyl) adipate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrogenchloride / water / 4 h / Reflux
2: 20 h / 200 - 210 °C / Dean-Stark
View Scheme
Adipic acid
124-04-9

Adipic acid

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

A

adipic acid mono-2-ethylhexyl ester
4337-65-9

adipic acid mono-2-ethylhexyl ester

B

di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

Conditions
ConditionsYield
With hydrogenchloride In water for 4h; Reflux;A 49 %Chromat.
B 46 %Chromat.
adipic acid mono-2-ethylhexyl ester
4337-65-9

adipic acid mono-2-ethylhexyl ester

10-ethyl-7-tetradecanol

10-ethyl-7-tetradecanol

A

di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

B

bis(1-hexyl-4-ethyloctyl) adipate

bis(1-hexyl-4-ethyloctyl) adipate

C

C28H54O4

C28H54O4

Conditions
ConditionsYield
at 200 - 210℃; for 20h; Dean-Stark;A 22 %Chromat.
B 15 %Chromat.
C 62 %Chromat.
di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

aniline
62-53-3

aniline

N-phenylazepane
40832-99-3

N-phenylazepane

Conditions
ConditionsYield
With methanesulfonic acid; hydrogen; tris(acetylacetonato)ruthenium(III); [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In 1,4-dioxane at 220℃; under 7500.75 Torr; for 42h;80 %Chromat.
di(2-ethylhexyl)adipate
103-23-1

di(2-ethylhexyl)adipate

A

2-octyl-cyclopentanone
40566-23-2

2-octyl-cyclopentanone

B

C15H26O3

C15H26O3

C

Oxalic acid, cyclohexylmethyl octyl ester

Oxalic acid, cyclohexylmethyl octyl ester

D

C18H32O5

C18H32O5

E

5-Methyl-4-methylene-hexahydro-pentalen-1-one
120587-85-1

5-Methyl-4-methylene-hexahydro-pentalen-1-one

F

2-cyclopentylidenecyclopentan-1-one
825-25-2

2-cyclopentylidenecyclopentan-1-one

Conditions
ConditionsYield
at 300℃; for 2h; Temperature; Pyrolysis; Autoclave;

103-23-1Relevant articles and documents

Nano-SO42-/TiO2catalyzed eco-friendly esterification of dicarboxylic acids

Ji, Xianbing,Chen, Yinxia,Shen, Zuoyuan

, p. 5769 - 5772 (2014)

Nano-SO42-/TiO2 was prepared by wet impregnation method. The structure and properties of the prepared nano-SO42-/TiO2catalyst was characterized by XRD, SEM, TEM and BET analysis. The catalytic activities of the catalysts were tested by the esterification of sebacic acid with 2-ethyl hexanol and a series of other dicarboxylic acid. The influence factors on the reaction, such as the catalyst calcination temperature, reaction temperature/time and the molar ratio of acid to alcohol were extensively explored. Nano-SO42-/TiO2prepared exhibited much higher catalytic activity in esterification reactions. By applying the optimized reaction condition, i.e. 160 C, 2 h, 5 wt % nano-SO42-/TiO2with a 1:3 molar ratio of sebacic acid to 2-ethyl hexanol, higher than 99 % isolated of the desired ester could be obtained.

Micro-flow nanocatalysis: synergic effect of TfOH@SPIONs and micro-flow technology as an efficient and robust catalytic system for the synthesis of plasticizers

Tashi, Maryam,Shafiee, Behnaz,Sakamaki, Yoshie,Hu, Ji-Yun,Heidrick, Zachary,Khosropour, Ahmad R.,Beyzavi, M. Hassan

, p. 37835 - 37840 (2018)

The combination of continuous flow technology with immobilizing of only 0.13?mol% of triflic acid (TfOH) on silica-encapsulated superparamagnetic iron oxide nanoparticles (SPIONs) under solvent-free conditions successfully provided a powerful, efficient, and eco-friendly route for the synthesis of plasticizers. The turnover frequency value in micro-flow conditions varied in the range of 948.7 to 7384.6 h?1 compared to 403.8 to 3099 h?1 for in-flask. This technique works efficiently, encouraging future applications of micro-flow nano-catalysis in green chemistry.

Lubricant base oil and ester compounds

-

Paragraph 0079; 0099; 0100, (2019/06/29)

[Problem] To provide: an ester compound having low viscosity, excellent fluidity even at low temperatures, and a high viscosity index; and a lubricating oil base oil that blends said compound therein. [Solution] The present invention provides an ester compound indicated by formula (I). Formula (I) (in formula (I), R1 indicates a C1–35 hydrocarbon group and at least one hydrogen in the hydrocarbon group can be independently substituted for a group indicated by formula (II)). Formula (II) (in formula (II), R2 indicates a C1–30 linear alkyl or a C3–30 branched alkyl.)

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