2-Chloro-4,6-diamino-1,3,5-triazine
Analytical reference substance, ≥97%
Reagent
Code: #116426
Alias
2-Chloro-4,6-diamino-1,3,5-triazine, Atrazine-desethyl-desisopropyl; 2-Chloro-4,6-Diamino-1,3,5-Triazine;
CAS Number
3397-62-4
blur_circular Chemical Specifications
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Molecular Information
Weight
145.55 g/mol
Formula
C₃H₄ClN₅
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Registry Numbers
EC Number
222-260-6
MDL Number
MFCD00006054
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Physical Properties
Melting Point
>320 °C(lit.)
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Storage & Handling
Density
1.700
Storage
-20℃
description Product Description
2-Chloro-4,6-diamino-1,3,5-triazine is primarily utilized in the synthesis of herbicides and other agricultural chemicals. Its structure allows it to act as a key intermediate in the production of compounds that inhibit weed growth effectively. Additionally, it finds application in the development of certain types of resins and polymers, where its triazine core contributes to the thermal stability and chemical resistance of the materials. In the field of dye manufacturing, it serves as a building block for creating colorants with specific properties, such as enhanced lightfastness and durability. The compound's reactivity also makes it useful in organic synthesis, particularly in the formation of heterocyclic compounds that are important in pharmaceuticals and agrochemicals.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 97-100 |
Appearance | White to Yellow Powder or Crystals |
Infrared Spectrum | Conforms To Structure |
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2-Chloro-4,6-diamino-1,3,5-triazine
2-Chloro-4,6-diamino-1,3,5-triazine is primarily utilized in the synthesis of herbicides and other agricultural chemicals. Its structure allows it to act as a key intermediate in the production of compounds that inhibit weed growth effectively. Additionally, it finds application in the development of certain types of resins and polymers, where its triazine core contributes to the thermal stability and chemical resistance of the materials. In the field of dye manufacturing, it serves as a building block for creating colorants with specific properties, such as enhanced lightfastness and durability. The compound's reactivity also makes it useful in organic synthesis, particularly in the formation of heterocyclic compounds that are important in pharmaceuticals and agrochemicals.
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