Exploring the Chemical Structure and Potential of 2-(4-Amino-2-nitroanilino)-ethanol
The intricate world of organic chemistry is built upon the understanding of molecular structures and their inherent reactivities. 2-(4-Amino-2-nitroanilino)-ethanol, identified by its CAS number 2871-01-4, is a compound that embodies this complexity, offering significant potential for various applications, particularly in the field of dyes. NINGBO INNO PHARMCHEM CO.,LTD. sheds light on the structural aspects and synthetic possibilities of this versatile chemical.
At its core, 2-(4-Amino-2-nitroanilino)-ethanol (C8H11N3O3) features a substituted aniline ring. The presence of an amino group (-NH2) and a nitro group (-NO2) on the aromatic ring, along with an ethanolamine chain attached to the aniline nitrogen, confers specific chemical properties. The amino group is nucleophilic, while the nitro group is electron-withdrawing, influencing the reactivity of the aromatic ring and the amino group itself. The ethanolamine moiety, with its hydroxyl (-OH) and secondary amine (-NH-) functionalities, provides sites for further chemical modification and can influence solubility and physical properties.
These functional groups are key to its primary application as a hair dye intermediate. In dye chemistry, substituted anilines are fundamental building blocks for chromophores – the parts of a molecule responsible for color. The specific arrangement of the amino, nitro, and ethanolamine groups in 2-(4-Amino-2-nitroanilino)-ethanol allows it to participate in coupling reactions and oxidative polymerization processes that lead to the formation of colored compounds used in hair dyeing. The high purity, often specified as ≥99.0% HPLC, is crucial because even minor structural variations or impurities can drastically alter the resulting color hue, intensity, or stability.
Beyond its role in hair dyes, the structural features of this compound suggest broader synthetic potential. The hydroxyl group can undergo esterification or etherification reactions, while the amino group can be acylated or involved in Schiff base formation. The nitro group can be reduced to another amino group, opening up possibilities for creating diamine derivatives. For chemists involved in custom synthesis or developing new chemical entities, understanding these potential transformations is vital. When manufacturers look to buy this chemical, they often consider not just its current applications but also its potential as a versatile building block for novel molecules.
The reliable supply of such intermediates is critical for research and development as well as commercial production. NINGBO INNO PHARMCHEM CO.,LTD. plays a role in making these essential chemicals accessible. By offering high-quality 2-(4-Amino-2-nitroanilino)-ethanol, suppliers enable chemists to explore its full synthetic potential, leading to advancements in materials science, pharmaceuticals, and beyond. The exploration of its chemical structure is an ongoing process that fuels innovation in numerous industrial sectors.
Perspectives & Insights
Core Pioneer 24
“When manufacturers look to buy this chemical, they often consider not just its current applications but also its potential as a versatile building block for novel molecules.”
Silicon Explorer X
“The reliable supply of such intermediates is critical for research and development as well as commercial production.”
Quantum Catalyst AI
“By offering high-quality 2-(4-Amino-2-nitroanilino)-ethanol, suppliers enable chemists to explore its full synthetic potential, leading to advancements in materials science, pharmaceuticals, and beyond.”