4-Amino-2,3-dimethylphenol, with the CAS number 3096-69-3, is an organic compound characterized by the presence of an amino group and two methyl groups attached to a phenolic ring. This compound typically appears as a solid, often in a crystalline form, and is known for its solubility in organic solvents while being less soluble in water. It exhibits properties typical of phenolic compounds, including the ability to participate in various chemical reactions such as oxidation and substitution. The amino group contributes to its basicity and potential reactivity, making it useful in various applications, including as an intermediate in dye synthesis and in the production of pharmaceuticals. Additionally, its structure allows for potential interactions with biological systems, which may be of interest in medicinal chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety measures should be observed when working with this substance in a laboratory setting.

4-Amino-2,3-dimethylphenol

3096-69-3: 2,3-Dimethyl-4-aminophenol, 2,3-Dimethyl-4-hydroxyaniline, 2,3-Xylenol, 4-amino-, 4-Amino-2,3-Dimethylphenol, 4-Hydroxy-2,3-dimethylaniline, NSC 143549, Phenol, 4-amino-2,3-dimethyl-

4-Amino-2,3-xylenol

4-Amino-2,3-xylenol is an oxidation product of acetaminophen and is a cytosolic protein. It has been shown to have cytotoxic effects in vitro on cells, specifically on the neonatal rat brain. 4-Amino-2,3-xylenol has also been shown to be a metabolite of lignocaine in vivo and may contribute to the drug's cardiotoxic effects. The metabolism of 4-amino-2,3-xylenol is mediated by hepatic S9 fractions and HPLC analysis. This metabolite can be detected in urine after administration of acetaminophen or lignocaine.

CAS 3096-69-3: 4-Amino-2,3-dimethylphenol

4-Amino-2,3-dimethylphenol

Ref: 10-F224261

4-Amino-2,3-xylenol

Ref: 3B-A0961

4-Amino-2,3-xylenol

Ref: 3D-DAA09669

Phenol, 4-amino-2,3-dimethyl-

Ref: IN-DA0031S3