2,4,6-Trimethyl-1,3-phenylenediamine丨CAS 3102-70-3

2,4,6-Trimethyl-1,3-phenylenediamine丨CAS 3102-70-3
Product Introduction:
Catalog No.: SS124091
CAS No.: 3102-70-3
Purity(HPLC): 99.5% min
Product Name: 2,4,6-Trimethyl-1,3-phenylenediamine
Molecular Formula: C9H14N2
Molecular Weight: 150.22
Synonym(s): 2,4-Diamino-1,3,5-trimethylbenzene
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 2,4,6-trimethyl-1,3-phenylenediamine丨cas 3102-70-3 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance Light yellow powder
Purity (HPLC) 99.5% min
Water Content 0.1% max
Melting Point 88°C min

 

 

 

Applications

 

2,4,6-Trimethyl-1,3-phenylenediamine is a key aromatic diamine used primarily in polymer chemistry, dye manufacturing, and chemical synthesis. In polymer applications, it serves as a curing agent or hardener for epoxy resins, polyurethane systems, and other thermosetting polymers, where it improves mechanical strength, thermal stability, and chemical resistance. In the dye and pigment industry, it acts as an intermediate for the synthesis of azo dyes, reactive dyes, and other colored compounds, providing controlled substitution patterns that influence color intensity and stability. Additionally, it is utilized in organic synthesis as a building block for heterocyclic compounds, pharmaceuticals, and specialty chemicals, where its diamine functionality allows for selective reactions such as condensation, alkylation, and acylation. Its solubility, thermal stability, and predictable reactivity make it suitable for both laboratory-scale research and industrial production.

 

Benefits

 

The benefits of this compound derive from its multifunctional aromatic structure, chemical stability, and versatility in synthesis. The diamine functionality allows for efficient cross-linking in polymer systems, enhancing mechanical and thermal properties of cured materials. Its methyl-substituted aromatic ring provides steric protection, reducing undesired side reactions and improving the stability of the final product. In dye synthesis, the defined substitution pattern allows precise control over color, solubility, and fastness properties, enabling high-quality pigment production. The compound's thermal and chemical stability ensures reliable handling and reproducibility across reactions, while its solubility in common organic solvents facilitates easy incorporation into various formulations. These features make it an indispensable intermediate for polymer curing, dye production, and complex organic synthesis.

 

Conclusion

 

In summary, 2,4,6-Trimethyl-1,3-phenylenediamine is a valuable aromatic diamine with applications in polymer curing, dye manufacturing, and organic synthesis. Its multifunctional structure, thermal stability, and synthetic versatility provide significant benefits, including improved polymer properties, precise control in dye synthesis, and efficient building block utility. By supporting high-quality product development and reliable chemical transformations, it continues to play an essential role in industrial chemistry, materials science, and specialty chemical production.

 

 

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