1,3-Benzenediamine, 2,4-dimethyl- is an organic compound characterized by the presence of two amino groups (-NH2) attached to a benzene ring, specifically at the 1 and 3 positions, along with two methyl groups (-CH3) at the 2 and 4 positions. This structure classifies it as a diamine and an aromatic compound. The presence of amino groups makes it a potential precursor for various chemical syntheses, including dyes and pharmaceuticals. It is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents due to the amino groups. The compound can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in organic synthesis. Safety considerations are important, as many aromatic amines can be hazardous, potentially posing risks such as skin irritation or toxicity. Proper handling and storage in a controlled environment are essential to mitigate any health risks associated with exposure.

1,3-Benzenediamine, 2,4-dimethyl-

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2,4-Dimethylbenzene-1,3-diamine

2,4-Dimethylbenzene-1,3-diamine is a chelating agent that forms a ring with metals. It is used in clinical chemistry as a test sample for the detection of metals in urine and plasma samples. 2,4-Dimethylbenzene-1,3-diamine has been shown to form hydrogen bonds with fatty acids and solid catalysts for reactions. The reaction products are mainly low energy compounds such as water, amines, and alcohols. This chemical has been shown to react with x-ray crystal structures at high energies to form nitrogen atoms. The clinical relevance of this compound is not known at this time.

CAS 13438-26-1: 1,3-Benzenediamine, 2,4-dimethyl-

1,3-Benzenediamine, 2,4-dimethyl-

Ref: IN-DA00HTB5

2,4-Dimethylbenzene-1,3-diamine

Ref: 10-F898009

2,4-Dimethylbenzene-1,3-diamine

Ref: 3D-NAA43826