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7237-83-4

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7237-83-4 Usage

Description

Tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate is a chemical compound with the molecular formula C21H18O12, characterized by its high reactivity and ability to form strong, durable bonds with other materials. It is known for its high thermal and chemical resistance, making it a valuable component in various industrial applications.

Uses

Used in Coatings Industry:
Tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate is used as a crosslinking agent for epoxy resin formulations, providing enhanced durability and performance in coatings.
Used in Adhesives Industry:
tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate is used as a crosslinking agent in epoxy resin formulations for adhesives, offering strong bonding capabilities and improved resistance to environmental factors.
Used in Composite Materials Industry:
Tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate is utilized as a crosslinking agent in the production of composite materials, contributing to their overall strength and stability.
Used in Electronic Materials Production:
tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate serves as a curing agent in the manufacturing of advanced electronic materials, ensuring proper hardening and performance of these materials.
Used in Plastic Compounds:
Tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate is used as a stabilizer in plastic compounds, enhancing their resistance to heat and chemicals, thus improving their overall quality and longevity.

Check Digit Verification of cas no

The CAS Registry Mumber 7237-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7237-83:
(6*7)+(5*2)+(4*3)+(3*7)+(2*8)+(1*3)=104
104 % 10 = 4
So 7237-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2.2HI.Zn/c1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9;;;/h3-8H,1-2H3;2*1H;/q-2;;;+2/p-2

7237-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(oxiran-2-ylmethyl) benzene-1,2,4-tricarboxylate

1.2 Other means of identification

Product number -
Other names Tris(oxiranylmethyl) benzene-1,2,4-tricarboxylate

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:7237-83-4 SDS

7237-83-4Downstream Products

7237-83-4Relevant articles and documents

Synthesizing method of triglycidyl tribenzoate

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Paragraph 0020-0029, (2019/02/04)

The invention discloses a synthesizing method of triglycidyl tribenzoate, and belongs to the field of organic synthesis. The synthesizing method comprises the following steps of (1) using trimelliticacid and epichlorohydrin as raw materials, using quaternary ammonium salt as a catalyst, using a protic solvent and/or a lewis acid metal salt as additives, and generating a chlorohydrin intermediate;(2) enabling the generated chlorohydrin intermediate to synthesize the triglycidyl tribenzoate under the functions of organic solvent and inorganic strong base. The synthesizing method has the advantages that by adding the additives into the esterification reaction, the yield rate of esterification reaction is increased, and the generation amount of byproducts is reduced, namely that the amount of byproducts in the esterification reaction can be obviously reduced by adding a proper amount of protic solvent, and the yield rate of esterification reaction can be increased by adding a proper amount of lewis acid; the purity of the obtained triglycidyl tribenzoate crude product can be effectively increased, the difficulty in subsequent purification is decreased, the operation of the two stepsis simple, the post-treatment is rapid and convenient, and the synthesizing method is suitable for the industrialized production.

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