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1,3,5-tris(2,3-epoxypropoxy)benzene is a chemical compound characterized by a benzene ring with three 2,3-epoxypropoxy groups attached at the 1, 3, and 5 positions. It is known for its ability to form strong, durable bonds, which makes it a versatile crosslinking agent in various industrial applications.

4223-14-7

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4223-14-7 Usage

Uses

Used in Adhesives Industry:
1,3,5-tris(2,3-epoxypropoxy)benzene is used as a crosslinking agent for enhancing the adhesive properties of various materials. Its strong bonding capability contributes to the creation of durable and long-lasting adhesives.
Used in Coatings Industry:
In the coatings industry, 1,3,5-tris(2,3-epoxypropoxy)benzene is utilized as a crosslinking agent to improve the durability and performance of coatings. This results in coatings with enhanced resistance to wear, chemicals, and environmental factors.
Used in Composites Industry:
1,3,5-tris(2,3-epoxypropoxy)benzene is employed as a crosslinking agent in the production of composite materials. Its use leads to the creation of composites with improved mechanical properties and structural integrity.
Used in Flame Retardants Manufacturing:
1,3,5-tris(2,3-epoxypropoxy)benzene is used as a key component in the manufacturing of flame retardants. Its chemical structure contributes to the development of flame-resistant materials, enhancing safety in various applications.
Used in Plasticizers Production:
In the production of plasticizers, 1,3,5-tris(2,3-epoxypropoxy)benzene is used to improve the flexibility and workability of plastics. Its incorporation into plasticizers results in materials with enhanced properties for specific applications.
Used in Specialty Chemicals Industry:
1,3,5-tris(2,3-epoxypropoxy)benzene is also utilized in the manufacturing of various specialty chemicals. Its unique chemical properties allow for the development of innovative products tailored to specific industry needs.
It is crucial to handle 1,3,5-tris(2,3-epoxypropoxy)benzene with care due to its potential health and environmental hazards if not properly managed. Proper safety measures and disposal methods should be adhered to when working with 1,3,5-tris(2,3-epoxypropoxy)benzene.

Check Digit Verification of cas no

The CAS Registry Mumber 4223-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4223-14:
(6*4)+(5*2)+(4*2)+(3*3)+(2*1)+(1*4)=57
57 % 10 = 7
So 4223-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O6/c1-10(16-4-13-7-19-13)2-12(18-6-15-9-21-15)3-11(1)17-5-14-8-20-14/h1-3,13-15H,4-9H2

4223-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[3,5-bis(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane

1.2 Other means of identification

Product number -
Other names EINECS 224-173-9

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:4223-14-7 SDS

4223-14-7Downstream Products

4223-14-7Relevant academic research and scientific papers

From a bio-based phosphorus-containing epoxy monomer to fully bio-based flame-retardant thermosets

Ménard, Rapha?l,Negrell, Claire,Fache, Maxence,Ferry, Laurent,Sonnier, Rodolphe,David, Ghislain

, p. 70856 - 70867 (2015)

In this work, phloroglucinol was used as a renewable resource to prepare an epoxy monomer and phosphorus containing reactive flame retardant (FR). These building blocks were reacted with diamines to obtain partly or fully bio-based flame retardant epoxy r

A facile synthesis of polyglycidyl ethers from polyols and epichlorohydrin

Kida,Yokota,Masuyama,Nakatsuji,Okahara

, p. 487 - 489 (2007/10/02)

The reaction of 1,1,1-tris(hydroxymethyl)ethane (1a), 2-ethyl-2-(hydroxymethyl)-1,3-propanediol (1b), pentaerythritol (1c), or 1,2,6-hexanetriol (1e) with epichlorohydrin in the presence of potassium hydroxide in dimethyl sulfoxide gave the corresponding tri- or tetraglycidyl ethers 3a-c, e in high yields. This procedure was also applicable to the preparation of the phenolic polyglycidyl ethers.

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