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2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine, also known as TPT or melamine, is a chemical compound characterized by the molecular formula C9H6N12. It is a white crystalline solid that exhibits insolubility in water and most organic solvents. 2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine is recognized for its versatile applications across various industries due to its unique molecular structure and properties.

27114-96-1

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27114-96-1 Usage

Uses

Used in Flame Retardant Materials:
2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine is used as a key component in the production of flame retardant materials for enhancing the fire resistance of various products. Its chemical structure contributes to the formation of a protective char layer that slows down the spread of flames.
Used in Resin, Adhesive, and Plastic Manufacturing:
In the manufacturing industry, 2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine is utilized as a raw material for producing resins, adhesives, and plastics. Its properties improve the durability, strength, and heat resistance of these materials, making them suitable for a wide range of applications.
Used as a Cross-Linking Agent in Melamine-Formaldehyde Resins:
2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine serves as an effective cross-linking agent in the production of melamine-formaldehyde resins. This role is crucial for creating strong, heat-resistant materials that are extensively used in the construction and automotive industries.
Used in High-Energy Materials for Rocket Propellants and Explosives:
2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine has been investigated for its potential use as a high-energy material in rocket propellants and explosives due to its high energy content. This application is still under research and development to ensure safety and efficiency.
Used in Chemical Research and Development:
2,4,6-tri(1H-pyrrol-1-yl)-1,3,5-triazine's unique molecular structure makes it a valuable building block for the synthesis of complex organic compounds in chemical research and development. It aids in the creation of new compounds with potential applications in various fields, including pharmaceuticals and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 27114-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,1 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27114-96:
(7*2)+(6*7)+(5*1)+(4*1)+(3*4)+(2*9)+(1*6)=101
101 % 10 = 1
So 27114-96-1 is a valid CAS Registry Number.

27114-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tri(pyrrol-1-yl)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names 2,4,6-tri(1h-pyrrol-1-yl)-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:27114-96-1 SDS

27114-96-1Relevant academic research and scientific papers

Synthesis of heteroaromatic derivatives with nitrogen atoms: Tripyrrolyl pyrimidine and tripyrrolyl[1,3,5]triazine

Lee,Lee,Jung,Hahn

, p. 501 - 504 (2013/02/22)

As a part of a research program related to the synthetic study of pharmacologically and photoconductively interesting pyrrole derivatives, we have synthesized 1-arylpyrroles (3a-e), 9-arylcarbazoles (4a-e), aminophenylpyrroles (6a,b), dipyrrolylbenzenes (7a-c), 2,4,6-tri-pyrrol-1- yl-pyrimidine (8) and 2,4,6-tri-pyrrol-1-yl[1,3,5]triazine (9). We proposed a plausible mechanism for the formation of 9-arylcarbazole.

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