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Atomfair Benzenesulfonic acid, 3-(acetylamino)-5-amino-4-hydroxy- C8H10N2O5S

Description 3-Acetamido-5-amino-4-hydroxybenzenesulfonic acid (CAS No. 40306-75-0) is a high-purity sulfonic acid derivative with the molecular formula C8H10N2O5S. This compound features a benzenesulfonic acid core substituted with acetamido, amino, and hydroxy functional groups, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its unique structure enables applications in dye synthesis, biochemical studies, and as a precursor for specialized reagents. Available in research-grade quality, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive experiments. Suitable for laboratory use only.

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Description

Description

3-Acetamido-5-amino-4-hydroxybenzenesulfonic acid (CAS No. 40306-75-0) is a high-purity sulfonic acid derivative with the molecular formula C8H10N2O5S. This compound features a benzenesulfonic acid core substituted with acetamido, amino, and hydroxy functional groups, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its unique structure enables applications in dye synthesis, biochemical studies, and as a precursor for specialized reagents. Available in research-grade quality, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive experiments. Suitable for laboratory use only.

  • CAS No: 40306-75-0
  • Molecular Formula: C8H10N2O5S
  • Molecular Weight: 246.24
  • Exact Mass: 246.03104260
  • Monoisotopic Mass: 246.03104260
  • IUPAC Name: 3-acetamido-5-amino-4-hydroxybenzenesulfonic acid
  • SMILES: CC(=O)NC1=CC(=CC(=C1O)N)S(=O)(=O)O
  • Synonyms: 3-(Acetylamino)-5-amino-4-hydroxybenzenesulfonic acid, Benzenesulfonic acid, 3-(acetylamino)-5-amino-4-hydroxy-, EINECS 254-879-2, NSC 229313, 3-Acetamido-5-amino-4-hydroxybenzenesulphonic acid

Application

3-Acetamido-5-amino-4-hydroxybenzenesulfonic acid is primarily used as a key intermediate in the synthesis of azo dyes and other colorants. Its reactive functional groups make it valuable for coupling reactions in organic chemistry. Researchers also employ it in biochemical studies involving sulfonated aromatic compounds. Additionally, it serves as a building block for pharmaceuticals and specialty chemicals requiring sulfonic acid derivatives.

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