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2,4,6-Tris(trichloromethyl)-1,3,5-triazine, with the molecular formula C6H3Cl9N3, is a white, crystalline chemical compound primarily recognized for its flame retardant properties. It is highly reactive and can emit toxic fumes of hydrogen chloride gas when subjected to heat or fire. Despite its utility, it has been identified to have potential environmental and health risks, including harm to aquatic organisms and the risk of bioaccumulation in the food chain, leading to strict regulatory measures in many countries.

6542-67-2

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6542-67-2 Usage

Uses

Used in Plastics Industry:
2,4,6-Tris(trichloromethyl)-1,3,5-triazine is used as a flame retardant additive for enhancing the fire resistance of various types of plastics. Its incorporation into plastic materials helps to slow down the spread of flames and reduce the intensity of fires, thereby improving safety standards for plastic products.
Used in Textile Industry:
In the textile sector, 2,4,6-Tris(trichloromethyl)-1,3,5-triazine serves as a flame retardant agent to treat fabrics and fibers. This treatment imparts fire-resistant properties to textiles, making them suitable for use in applications where fire safety is a critical concern, such as in upholstery, carpets, and protective clothing.

Check Digit Verification of cas no

The CAS Registry Mumber 6542-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6542-67:
(6*6)+(5*5)+(4*4)+(3*2)+(2*6)+(1*7)=102
102 % 10 = 2
So 6542-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C6Cl9N3/c7-4(8,9)1-16-2(5(10,11)12)18-3(17-1)6(13,14)15

6542-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-Tris(Trichloromethyl)-1,3,5-Triazine

1.2 Other means of identification

Product number -
Other names 2,4,6-tris(trichloromethyl)-1,3,5-triazine

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:6542-67-2 SDS

6542-67-2Relevant academic research and scientific papers

Triazine based photoactive compound containing oxime ester

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Page/Page column 5-6, (2008/06/13)

The present invention relates to a triazine based photoactive compound containing an oxime ester group. The compound according to the present invention is a photoactive compound containing both an oxime ester group and a triazine group in one molecule, ha

TRIAZINE BASED PHOTOACTIVE COMPOUND CONTAINING OXIME ESTER

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Page/Page column 11, (2008/06/13)

The present invention relates to a triazine based photoactive compound containing an oxime ester group. The compound according to the present invention is a photoactive compound containing both an oxime ester group and a triazine group in one molecule, ha

SYNTHESIS AND PROPERTIES OF sym-TRIAZENE DERIVATIVES 12. SYNTHESIS OF 2,4-BIS(TRICHLOROMETHYL)-6-SUBSTITUTED sym-TRIAZENES CONTAINING A STERICALLY HINDERED PHENOL GROUP

Kelarev, V. I.,Koshelev, V. N.,Belov, N. V.,Malova, O. V.,Karakhanov, R. A.

, p. 218 - 221 (2007/10/02)

6-Substituted 2,4-bis(trichloromethyl)-sym-triazenes containing the 2,6-di-tert-butylphenol group are synthesized by simultaneous cyclotrimerization of trichloroacetonitrile with the nitrile or thiocyanate derivative of the sterically hindered phenol in the presence of gaseous HCl.Significant amounts of 2,4,6-tris(trichloromethyl)-sym-triazene are formed as a by-product.

Synthesis and Properties of sym-Triazine Derivatives. 8. Synthesis of Amino and Alkoxy Derivatives of sym-Triazine Containing Fragments of a Sterically-Hindered Phenol from 2,4-Bis(trichloromethyl)-sym-triazines

Kelarev, V. I.,Yakh'ya, F. Laauad,Karakhanov, R. A.,Golubeva, I. A.,Vishnyakova, T. P.,Malova, O. V.

, p. 556 - 561 (2007/10/02)

The reactions of 2,4-bis(trichloromethyl)-6-substituted sym-triazines with several amino and hydroxy derivatives of 2,6-di-tert-butylphenol were studied.It is shown that, depending on the reaction conditions, one or both trichloromethyl groupings in the starting sym-triazines are replaced.

SYNTHESIS OF 2-ALKYL-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINES CONTAINING LONG-CHAIN NORMAL ALKYL RADICALS

Kelarev, V. I.,Dibi, Ammar,Lunin, A. F.,Malova, O. V.

, p. 1189 - 1193 (2007/10/02)

2-Alkyl-4,6-bis(trichloromethyl)-1,3,5-triazines containing long-chain normal alkyl radicals were synthesized by the joint cyclotrimerization of trichloroacetonitrile with the nitriles of higher aliphatic acids in the presence of gaseous hydrogen chloride. 2,4,6-Tris(trichloromethyl)-1,3,5-triazine was formed in considerable quantities as side product.

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