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• 2. Fluorescent Au nanoclusters stabilized by silane: facile synthesis, color-tunability and photocatalytic properties
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• 4. Progress and perspectives of electrochemical insights for C–H and N–H sulfonylation
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols Benzenediols Catechols
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols Catechols

Comprehensive Analysis of 4-Aminocatechol (CAS No. 13047-04-6): Properties, Applications, and Research Insights

4-Aminocatechol (CAS No. 13047-04-6) is a biologically significant aromatic compound featuring both amino and catechol functional groups. This dual functionality makes it a versatile intermediate in organic synthesis, pharmaceutical research, and material science. With the growing interest in sustainable chemistry and bioactive molecules, 4-Aminocatechol has garnered attention for its potential in antioxidant applications and enzyme inhibition studies. Researchers are increasingly exploring its role in neuroprotective agents and polymeric materials, aligning with trends in green chemistry and drug discovery.

The molecular structure of 4-Aminocatechol (C₆H₇NO₂) consists of a benzene ring substituted with two hydroxyl groups (catechol) and an amino group at the 4-position. This configuration enables unique chelation properties, making it valuable in metal-ion binding applications, such as catalysis and sensor development. Recent studies highlight its utility in designing biodegradable polymers, a hot topic in environmental science. Its redox-active nature also positions it as a candidate for energy storage materials, addressing the surge in demand for renewable energy solutions.

In pharmaceutical contexts, 4-Aminocatechol derivatives are investigated for their anti-inflammatory and neuroregenerative potential. A 2023 study published in the Journal of Medicinal Chemistry identified its analogs as modifiers of dopaminergic pathways, relevant to Parkinson’s disease research. This aligns with frequent search queries like "natural antioxidants for brain health" and "catecholamines in neurology." Additionally, its UV-absorbing properties make it a candidate for cosmetic formulations, tapping into the booming clean beauty market.

From a synthetic perspective, 4-Aminocatechol is often prepared via electrophilic aromatic substitution or reductive amination of catechol derivatives. Optimizing its yield and purity remains a focus in process chemistry, as reflected in search trends like "high-yield aminophenol synthesis". Its stability under physiological conditions also makes it a benchmark in bioconjugation techniques, a trending topic in biotechnology forums.

Environmental and safety profiles of 4-Aminocatechol are rigorously evaluated. While not classified as hazardous, its biodegradability and ecotoxicity data are critical for industrial adoption. Regulatory databases like REACH and EPA’s CompTox provide updated guidelines, addressing common queries such as "safe handling of aminophenols". Future research may explore its carbon-capture potential, leveraging its metal-coordination ability—a niche yet growing area in climate tech.

• 6119-34-2(Phenoxy, 4-amino-)
• 159661-41-3(1,2-Benzenediol, 4,5-diamino-)
• 111672-42-5(1,2-benzenediol, compd. with 1,4-benzenediamine (1:1))
• 4956-56-3(4-Aminocatechol Hydrochloride)
• 158627-59-9(4-Aminobenzene-1,2-diol hydrobromide)
• 51-81-0(3-Aminophenol hydrochloride)
• 285132-88-9(4-Aminophenol-d7)
• 91696-55-8(1,4-benzenediol, reaction products with aniline, branched octyl derivs.)
• 25167-12-8(Phenol, diamino-)
• 20734-67-2(5-aminobenzene-1,3-diol)