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2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine, also known as hexafluoroisopropylidene-diphenoxytriazine, is a synthetic chemical compound that is widely recognized for its high stability and non-reactivity. It is a white crystalline solid with exceptional thermal stability, chemical resistance, and UV stability, which makes it a valuable component in the production of various materials.

2663-96-9

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2663-96-9 Usage

Uses

Used in Polymer and Coating Production:
2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine is used as a building block for the synthesis of polymers and coatings. Its high stability and resistance properties contribute to the creation of durable and long-lasting products in this industry.
Used in Specialty Plastics Manufacturing:
In the plastics industry, 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine is used as an ingredient for the production of specialty plastics. Its thermal and chemical stability enhance the performance and longevity of the plastics, making them suitable for specific applications that require these properties.
Used in Adhesives and Adhesion Promoters:
2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine is employed as a component in the formulation of adhesives and adhesion promoters. Its ability to resist heat and chemicals makes it an ideal additive for creating strong bonds in various applications.
Used as a Flame Retardant:
In the field of fire safety, 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine is used as a flame retardant. Its inherent properties help to slow down the spread of fire and provide additional safety measures in materials that are prone to ignition.
Used in Specialty Chemicals and Materials Production:
2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine is also utilized in the production of specialty chemicals and materials. Its unique characteristics make it a valuable component in the development of advanced materials with specific properties tailored for various industries.
It is important to handle 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine with caution, as there is limited data available on its potential environmental and health impacts. Proper safety measures should be taken to minimize any risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 2663-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2663-96:
(6*2)+(5*6)+(4*6)+(3*3)+(2*9)+(1*6)=99
99 % 10 = 9
So 2663-96-9 is a valid CAS Registry Number.

2663-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(2,3,4,5,6-pentafluorophenoxy)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names 2,4,6-tris-pentafluorophenoxy-[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:2663-96-9 SDS

2663-96-9Downstream Products

2663-96-9Relevant academic research and scientific papers

Modification of channel structures by fluorination

Reichenbaecher, Katharina,Suess, Heike I.,Stoeckli-Evans, Helen,Bracco, Silvia,Sozzani, Piero,Weber, Edwin,Hulliger, Juerg

, p. 393 - 397 (2007/10/03)

Two perfluorinated triazines [2,4,6-tris(p-bromotetrafluorophenoxy)-1,3,5- triazine (2) and 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine (3)] were synthesised to study their crystal structure and inclusion character. Compound 3 forms channel inclusions with the solvents p-xylene and p-chlorotoluene, showing a stoichiometry of 2:1 (host:guest). The channels have dimensions of 7. 6 × 3 A2. The host-guest interactions, perfluorophenyl-phenyl stacking, F...H- and CH...π(perfluorophenyl) contacts, were revealed by the crystallographic and solid state NMR spectroscopy studies. The reversibility of the sorption process through the gas phase could be demonstrated by X-ray diffraction. In contrast to the pentafluorinated compound 3, the tetrafluorinated one (2) showed no inclusions with a number of typical solvents.

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