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137-89-3

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137-89-3 Usage

Description

BIS(2-ETHYLHEXYL)ISOPHTHALATE, also known as Di(2-ethylhexyl) isophthalate, is a clear light yellow viscous liquid with chemical properties that include a water solubility of less than 0.1 g/100mL at 16℃. It is a colorless liquid.

Uses

Used in Plastic Industry:
BIS(2-ETHYLHEXYL)ISOPHTHALATE is used as a plasticizer for enhancing the flexibility, workability, and durability of various types of plastics. Its chemical properties allow it to be an effective additive in the production of flexible PVC and other polymers.
Used in Lubricant Industry:
In the lubricant industry, BIS(2-ETHYLHEXYL)ISOPHTHALATE is used as an additive to improve the viscosity, stability, and performance of lubricants. Its ability to mix with various base oils makes it a valuable component in the formulation of high-quality lubricants for different applications.
Used in Cosmetics and Personal Care Industry:
BIS(2-ETHYLHEXYL)ISOPHTHALATE is used as an emollient and viscosity-increasing agent in the cosmetics and personal care industry. It helps to provide a smooth and consistent texture to creams, lotions, and other skincare products, enhancing their overall performance and feel on the skin.
Used in Medical Applications:
BIS(2-ETHYLHEXYL)ISOPHTHALATE can be used in the medical field as a component in the production of certain medical devices and equipment, where its chemical properties contribute to the desired characteristics of the final product, such as flexibility and durability.
Used in Adhesives and Sealants Industry:
In the adhesives and sealants industry, BIS(2-ETHYLHEXYL)ISOPHTHALATE is used as a plasticizer to improve the flexibility, adhesion, and workability of various adhesive and sealant formulations. Its compatibility with different types of polymers makes it a versatile additive in this industry.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

BIS(2-ETHYLHEXYL)ISOPHTHALATE 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.

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition BIS(2-ETHYLHEXYL)ISOPHTHALATE emits acrid smoke and irritating fumes.

Fire Hazard

BIS(2-ETHYLHEXYL)ISOPHTHALATE is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 137-89-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137-89:
(5*1)+(4*3)+(3*7)+(2*8)+(1*9)=63
63 % 10 = 3
So 137-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H38O4/c1-5-9-12-19(7-3)17-27-23(25)21-14-11-15-22(16-21)24(26)28-18-20(8-4)13-10-6-2/h11,14-16,19-20H,5-10,12-13,17-18H2,1-4H3

137-89-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (91344)  Bis(2-ethylhexyl) isophthalate  analytical standard

  • 137-89-3

  • 91344-100MG

  • 869.31CNY

  • Detail

137-89-3SDS

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) benzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names DOIP

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:137-89-3 SDS

137-89-3Downstream Products

137-89-3Relevant articles and documents

Production of Copolyester Monomers from Plant-Based Acrylate and Acetaldehyde

Yuan, Lin,Hu, Yancheng,Zhao, Zhitong,Li, Guangyi,Wang, Aiqin,Cong, Yu,Wang, Feng,Zhang, Tao,Li, Ning

supporting information, (2021/12/14)

PCTA is an important copolyester that has been widely used in our daily necessities. Currently, its monomers are industrially produced from petroleum-derived xylene. To reduce the reliance on fossil energy, we herein disclose an alternative route to acces

PLASTICIZER COMPOSITION, RESIN COMPOSITION AND METHOD FOR PREPARING THEREOF

-

Paragraph 0031; 0032, (2018/02/03)

The present invention relates to a plasticizer composition, a resin composition and a method for preparing thereof. The present invention can provide a plasticizer composition, which can improve properties required to the plasticizer composition contained in a vinyl chloride-based resin composition, such as plasticizing efficiency, volatile loss, and migration resistance, to a level equal to or better than the existing plasticizer composition, and a resin composition comprising thereof.

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

Ji, Xianbing,Chen, Yinxia,Shen, Zuoyuan

, p. 5769 - 5772 (2014/12/11)

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.

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