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TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is a specialty chemical denoted as a sulfur-containing triazinetrione. It is primarily used as a crosslinking agent due to its high reactivity toward polymers. The substance contains three mercaptopropionyloxy groups linked to an isocyanurate ring which drives its reactivity and functional properties. The mercaptopropionyl groups can interact with a variety of substrates to form covalent linkages, enabling the production of diverse crosslinked materials with enhanced mechanical and thermal resistance. Moreover, the isocyanurate ring in this chemical imparts additional thermal stability.

36196-44-8

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36196-44-8 Usage

Uses

Used in Adhesives Industry:
TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is used as a crosslinking agent for improving the mechanical and thermal resistance of adhesives. Its reactivity with various substrates allows for the formation of covalent linkages, resulting in stronger and more durable adhesives.
Used in Coatings Industry:
TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is used as a crosslinking agent in the production of coatings. Its ability to form covalent linkages with substrates enhances the mechanical and thermal properties of the coatings, providing better protection and durability.
Used in Rubber Industry:
TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is used as a crosslinking agent in the manufacturing of rubber products. The reactivity of the mercaptopropionyl groups with polymers results in rubber materials with improved mechanical strength and thermal stability.
Used in Plastics Industry:
TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is used as a crosslinking agent in the production of plastic materials. The formation of covalent linkages with polymers leads to plastics with enhanced mechanical properties and thermal resistance, making them suitable for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 36196-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,9 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36196-44:
(7*3)+(6*6)+(5*1)+(4*9)+(3*6)+(2*4)+(1*4)=128
128 % 10 = 8
So 36196-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H27N3O9S3/c22-13(1-10-31)28-7-4-19-16(25)20(5-8-29-14(23)2-11-32)18(27)21(17(19)26)6-9-30-15(24)3-12-33/h31-33H,1-12H2

36196-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2,4,6-trioxo-3,5-bis[2-(3-sulfanylpropanoyloxy)ethyl]-1,3,5-triazinan-1-yl]ethyl 3-sulfanylpropanoate

1.2 Other means of identification

Product number -
Other names tris[2-(3-mercaptopropionyloxy)ethyl] isocyanurate

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:36196-44-8 SDS

36196-44-8Downstream Products

36196-44-8Relevant academic research and scientific papers

Activated dopamine derivatives as primers for adhesive-patch fixation of bone fractures

Olofsson,Granskog,Cai,Hult,Malkoch

, p. 26398 - 26405 (2016/03/25)

For the stabilization of complex bone fractures, tissue adhesives are an attractive alternative to conventional implants, often consisting of metal plates and screws whose fixation may impose additional trauma on the already fractured bone. This study reports on the synthesis and evaluation of activated dopamine derivatives as primers for fiber-reinforced-adhesive patches in bone-fracture stabilization strategies. The performance of synthesized dopamine derivatives are evaluated with regard to the adhesive shear strength of formed bone patches, as well as cell viability and surface properties. Dopamine-derived primers with methacrylamide, allyl, and thiol functional groups were found to significantly increase the adhesive shear strength of adhesive patches. Furthermore, deprotonation of the primer solution was determined to be essential in order to achieve good adhesion. In conclusion, the primer solutions that were found to give the best adhesion were the once where dopa-thiol was used in combination with either dopa-methacrylamide or dopa-allyl, resulting in shear bond strengths of 0.29 MPa.

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