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6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine, commonly known as Melamine, is a white crystalline solid with the molecular formula C6H9N3. It is a chemical compound that is widely used in various industries due to its unique properties.

29366-76-5

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29366-76-5 Usage

Uses

Used in Plastics Industry:
6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is used as a key component in the production of plastics. Its high heat resistance and durability make it an ideal material for creating long-lasting plastic products.
Used in Adhesives Industry:
In the adhesives industry, 6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is used as a binding agent. Its strong adhesive properties allow it to effectively bond various materials together.
Used in Flame Retardants Industry:
6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is used as a flame retardant in various applications. Its ability to resist heat and flames makes it a valuable component in creating fire-resistant products.
Used in Kitchenware and Tableware Industry:
Due to its durability and heat-resistant properties, 6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is used in the manufacturing of kitchenware and tableware. It ensures that these products can withstand high temperatures and last for a long time.
Used in Fertilizer Industry:
6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is utilized as a fertilizer. It provides essential nutrients to plants, promoting their growth and development.
Used in Paper and Textile Industry:
In the paper and textile industry, 6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine is used to enhance the quality and durability of products. Its heat-resistant and durable properties make it an ideal material for creating long-lasting paper and textile products.
However, it is important to note that melamine has been the subject of controversy due to its presence in certain food products and its potential health hazards when consumed in high quantities. Therefore, it is crucial to ensure that the use of melamine in various industries is strictly regulated and controlled to minimize any potential risks to human health.

Check Digit Verification of cas no

The CAS Registry Mumber 29366-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29366-76:
(7*2)+(6*9)+(5*3)+(4*6)+(3*6)+(2*7)+(1*6)=145
145 % 10 = 5
So 29366-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N5/c1-6-3-2-4-7(5-6)8-13-9(11)15-10(12)14-8/h2-5H,1H3,(H4,11,12,13,14,15)

29366-76-5SDS

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 6-(m-tolyl)-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names -

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:29366-76-5 SDS

29366-76-5Downstream Products

29366-76-5Relevant academic research and scientific papers

2,4,6-trisubstituted-1,3,5-s-triazine compound and preparation and application thereof

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Paragraph 0028; 0057, (2021/10/05)

The invention provides a 2,4,6-trisubstituted-1,3,5-s-triazine compound as well as preparation and application thereof, and biguanide or dimethyl biguanide hydrochloride is used as an initial raw material to react with a cyano compound under an alkaline condition to prepare the 2,4,6-trisubstituted-1,3,5-s-triazine compound. The invention provides a simple and convenient synthetic method of a 2,4,6-trisubstituted-1,3,5-s-triazine compound, and the compound provided by the invention can be applied to preparation of an anti-myelogenous leukemia medicine, namely an enasidenib medicine. Compared with the prior art, the method for preparing the enasidenib has the advantages that two-step reaction is reduced, the use of a halogenating reagent is avoided, and the method is a green and environment-friendly chemical process. The structural formula I is shown in the specification.

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