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Diallyl itaconate is a versatile chemical compound derived from itaconic acid and allyl alcohol. It is known for its ability to improve the mechanical and thermal properties of polymers, making it a key ingredient in the production of adhesives, coatings, and composite materials. Its compatibility with different chemical compounds and its use as a crosslinking agent and monomer in the synthesis of various copolymers make diallyl itaconate an important building block in the development of advanced materials for various applications.

2767-99-9

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2767-99-9 Usage

Uses

Used in Polymer and Resin Production:
Diallyl itaconate is used as a crosslinking agent for enhancing the mechanical and thermal properties of polymers and resins. Its incorporation into these materials results in improved performance and durability.
Used in Adhesives and Coatings:
Diallyl itaconate is used as a key ingredient in the production of adhesives and coatings, where its ability to improve the mechanical and thermal properties of these materials contributes to their effectiveness and longevity.
Used in Composite Materials:
In the manufacturing of composite materials, diallyl itaconate is utilized to enhance the overall performance of the composite, providing improved strength and thermal stability.
Used in Specialty Chemicals and Pharmaceuticals:
Diallyl itaconate is also used in the production of specialty chemicals and pharmaceuticals, where its versatility and compatibility with different chemical compounds make it an important building block for the development of advanced materials in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2767-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2767-99:
(6*2)+(5*7)+(4*6)+(3*7)+(2*9)+(1*9)=119
119 % 10 = 9
So 2767-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-4-6-14-10(12)8-9(3)11(13)15-7-5-2/h4-5H,1-3,6-8H2

2767-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name DIALLYL ITACONATE

1.2 Other means of identification

Product number -
Other names 2-methylenesuccinic acid diallyl 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:2767-99-9 SDS

2767-99-9Downstream Products

2767-99-9Relevant academic research and scientific papers

UV-thermal dual cured anti-bacterial thiol-ene networks with superior performance from renewable resources

Dai, Jinyue,Ma, Songqi,Zhu, Lixia,Wang, Sheng,Yang, Lijing,Song, Zhenlun,Liu, Xiaoqing,Zhu, Jin

, p. 215 - 222 (2017)

Bio-based anti-bacterial cross-linked films with superior properties were prepared via UV-thermal induced thiol-ene “click” reaction of diallyl itaconate (DAI), eugenol allyl ether (EAE) with trimethylolpropane tris (3-mercaptopropionate). DAI and EAE were made from one-step reaction of itaconic acid and eugenol with allyl bromide, respectively. The curing behaviors studied by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) and gel content measurement illustrated that UV-thermal dual cure technology made the thiol-ene reaction more completely and produced films with higher performance compared with UV cure technology. The investigation of the thermal and mechanical properties of the cross-linked films by DSC, thermogravimetric analysis (TGA) and tensile test indicated that the glass transition temperature, tensile strength and modulus of the films were significantly improved after introducing DAI, and all the films exhibited similar and high thermal stability. Meanwhile, these bio-based polymer films showed excellent efficiency in killing common bacterias, e.g. S.?aureus and E.?coli in the dynamic shake test.

itaconic base three double bond compound and its preparation method and application

-

Paragraph 0046; 0047, (2016/10/07)

The invention discloses an itaconic acid-based three double bond compound with the structure represented by formula I. The invention also discloses an application of an itaconic acid-based triepoxy compound. Epoxy groups are introduced to the itaconic acid-based three double bond compound to obtain the itaconic acid-based triepoxy compound with the structure represented by formula II. The invention also discloses a preparation method of the itaconic acid-based three double bond compound, and a preparation method of the itaconic acid-based triepoxy compound. The preparation methods have the advantages of simplicity, easy implementation and control, reduction or avoiding of the use of petrochemical products through the synthesis using renewable itaconic acid as a raw material, resource saving and environmental protection. In the invention, the itaconic acid-based three double bond compound and the itaconic acid-based triepoxy compound can be used in thermosetting resins.

An efficient and regiospecific esterification of dioic acids using PTSA

Rama Devi,Rajaram

, p. 294 - 296 (2007/10/03)

Regiospecific mono alkyl esters of dioic acids have been obtained in excellent yield using PTSA as a catalyst. This method is mild and simpler than the previous methods.

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