Date published: 2026-5-22

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2-Methyl-m-phenylenediamine (CAS 823-40-5)

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Alternate Names:
2,6-Diaminotoluene
CAS Number:
823-40-5
Molecular Weight:
122.17
Molecular Formula:
C7H10N2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Methyl-m-phenylenediamine is a colorless solid with the molecular formula C7H10N2. This organic compound finds versatile applications in various fields due to its diverse properties. Primarily, 2-Methyl-m-phenylenediamine is widely utilized in the synthesis of numerous compounds, including dyes and polymers, making it an essential ingredient in these industries. Furthermore, it plays a significant role as a corrosion inhibitor in various industrial applications, providing protection against corrosion-related damage. Its importance extends to the realm of scientific research, where it is employed in the synthesis of dyes and polymers, contributing to advancements in these fields. Notably, it facilitates the production of compounds such as p-nitroaniline, p-aminonitrobenzene, and p-aminophenol, which are pivotal in various chemical processes. Beyond its utility in industrial and research applications, 2-Methyl-m-phenylenediamine exhibits notable biochemical effects. It acts as both a reductant and a ligand in biochemical reactions, demonstrating its versatility in catalyzing various chemical transformations. Additionally, it boasts antioxidant properties, making it an effective agent in combating oxidative stress. 2-Methyl-m-phenylenediamine′s multifaceted nature makes it an indispensable compound with extensive applications across industries, research, and medicinal fields, contributing to various scientific advancements and practical solutions.


2-Methyl-m-phenylenediamine (CAS 823-40-5) References

  1. Discovery of 2,4-pyrimidinediamine derivatives as potent dual inhibitors of ALK and HDAC.  |  Pan, T., et al. 2021. Eur J Med Chem. 224: 113672. PMID: 34237620
  2. Designing tailored combinations of structural units in polymer dielectrics for high-temperature capacitive energy storage.  |  Wang, R., et al. 2023. Nat Commun. 14: 2406. PMID: 37100776
  3. Chemical oxidative polymerization of m-phenylenediamine and its derivatives using aluminium triflate as a co-catalyst  |  Ismael Amer, Desmond Austin Young, Hermanus C.M. Vosloo. 2013. European Polymer Journal. 49: 3251-3260.
  4. Synthesis, antimicrobial and antioxidant activities of some 5-pyrazolone based Schiff bases  |  Narsidas Parmar a, Shashikant Teraiya a, Rikin Patel a, Hitesh Barad a, Harshur Jajda b, Vasudev Thakkar b. 2015. Journal of Saudi Chemical Society. 19: 36-41.
  5. Synthesis and characterization of new polymers derived from 2-methyl-m-phenylenediamine as an effective adsorbent for cationic dye removal  |  Hatice Karaer Yağmur a b, İsmet Kaya. 2020. Arabian Journal of Chemistry. 13: 8183-8199.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Methyl-m-phenylenediamine, 5 g

sc-230535
5 g
$30.00