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2,4,6-Tris(tert-butylperoxy)-1,3,5-triazine is a chemical compound with the molecular formula C12H24N6O3. It is an organic peroxide, which means it contains oxygen-oxygen single bonds and is used as a catalyst in the polymerization process. 2,4,6-TRIS(TERT-BUTYLPEROXY)-1,3,5-TRIAZINE is also known as a curing agent for epoxy resins, which are used in various applications such as adhesives, coatings, and composite materials. Due to its peroxide nature, it is sensitive to heat, shock, and friction, and can be hazardous if not handled properly. It is important to store and use this chemical in a controlled environment, following safety guidelines to prevent potential risks.

854-44-4

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854-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854-44-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 854-44:
(5*8)+(4*5)+(3*4)+(2*4)+(1*4)=84
84 % 10 = 4
So 854-44-4 is a valid CAS Registry Number.

854-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIS(TERT-BUTYLPEROXY)-1,3,5-TRIAZINE

1.2 Other means of identification

Product number -
Other names Tri-tert-butylperoxy-1.3.5-triazin

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:854-44-4 SDS

854-44-4Relevant academic research and scientific papers

Organic Peroxides. Part 12. The Preparation and Properties of Some Triazinyl Peroxides

Davies, Alwyn G.,Sutcliffe, Roger

, p. 1512 - 1519 (2007/10/02)

The triazinyl peroxides (A; X=Y=OOBut; X=OMe, Y=OOBut; X=Y=OMe; X=NEt2, Y=OOBut; X=Y=NEt2) and (B) have been prepared from the reaction between the appropriate peroxidic nucleophile and chlorotriazine.The structures of the peroxides are confirmed by their 13C n.m.r. spectra, and by the recovery of t-butyl hydroperoxide when the peroxides (A; X=Y=OOBut; X=OMe, Y=OOBut) were hydrolysed. .These peroxides are thermally stable up to ca. 90 deg C.Photolysis of the peroxides (A) gives the radical ButO. and XYC3N3O..The e.s.r. spectra of the triazinoxyl radicals could not be observed, but the adducts XYC3N3OCH2CH2. and XYC3N3OP.(OMe)3, which they form with ethylene and with trimethyl phosphite, respectively, were detected.It is suggested that these properties imply that the radicals have a ?-O rather than a ?-delocalised structure.

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