Cas no 31432-60-7 (N-Nitro-diphenylamine)

N-Nitro-diphenylamine is a nitro-substituted aromatic amine primarily used as an intermediate in organic synthesis and chemical manufacturing. Its key advantages include its role as a precursor in the production of dyes, agrochemicals, and specialty chemicals due to its stable nitro-functionalized aromatic structure. The compound exhibits moderate reactivity, allowing for selective transformations in synthetic pathways. Its thermal stability and compatibility with various solvents make it suitable for controlled reactions in industrial applications. Additionally, N-Nitro-diphenylamine serves as a model compound in research for studying nitro-aromatic reactivity and degradation processes. Proper handling is essential due to its potential toxicity and environmental considerations.
N-Nitro-diphenylamine structure
N-Nitro-diphenylamine structure
Product Name:N-Nitro-diphenylamine
CAS No:31432-60-7
MF:C12H10N2O2
MW:214.220002651215
CID:298998
PubChem ID:14971188
Update Time:2025-11-05

N-Nitro-diphenylamine Chemical and Physical Properties

Names and Identifiers

    • Benzenamine,N-nitro-N-phenyl-
    • N-Nitro-diphenylamine
    • N,N-diphenylnitramide
    • N-Nitro-diphenylamin
    • Benzenamine,N-nitro-N-phenyl
    • Diphenylnitramin
    • diphenylnitrosamine
    • N,N-diphenylnitramine
    • nitrodiphenyl amine
    • N-Nitro-N-phenyl-benzemamine
    • J-018427
    • DTXSID80566270
    • AKOS030255471
    • 31432-60-7
    • FT-0672762
    • SCHEMBL564828
    • DB-266529
    • Inchi: 1S/C12H10N2O2/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
    • InChI Key: AYLBVKUPVXVTSO-UHFFFAOYSA-N
    • SMILES: [O-][N+](N(C1C=CC=CC=1)C1C=CC=CC=1)=O

Computed Properties

  • Exact Mass: 214.07400
  • Monoisotopic Mass: 214.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 210
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4.1
  • Topological Polar Surface Area: 49.1?2

Experimental Properties

  • Melting Point: 81-82°C
  • Stability/Shelf Life: Moisture and Temperature Sensitive
  • PSA: 49.06000
  • LogP: 3.53960

N-Nitro-diphenylamine Customs Data

  • HS CODE:2928000090
  • Customs Data:

    China Customs Code:

    2928000090

    Overview:

    2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

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Additional information on N-Nitro-diphenylamine

N-Nitro-diphenylamine and Its Applications in CAS No. 31432-60-7 Research

N-Nitro-diphenylamine is a synthetic organic compound characterized by its molecular structure, which consists of a diphenylamine core with a nitro group attached to the nitrogen atom. This compound, with its CAS No. 31432-60-7 identifier, has garnered attention in pharmaceutical and materials science research due to its unique chemical properties and potential applications. Recent studies have explored its role in functional materials, catalytic processes, and as a precursor for advanced chemical synthesis, highlighting its significance in modern biomedical and chemical engineering fields.

One of the key areas of N-Nitro-diphenylamine research involves its use in the development of polymer-based materials. A 2023 study published in the Journal of Materials Chemistry demonstrated that N-Nitro-diphenylamine derivatives exhibit exceptional thermal stability and electrical conductivity, making them suitable for applications in flexible electronics and energy storage devices. These findings underscore the compound's potential to contribute to innovative material design and nanotechnology advancements.

Additionally, N-Nity-diphenylamine has been investigated for its role in electrochemical systems. Researchers at the University of Tokyo recently reported that the compound serves as an effective electron acceptor in organic photovoltaic cells, enhancing energy conversion efficiency. This application aligns with global efforts to develop renewable energy technologies and sustainable chemical processes. The integration of N-Nitro-diphenylamine into such systems highlights its versatility and relevance to environmental science and green chemistry.

The synthesis of N-Nitro-diphenylamine has also been a focus of recent organic chemistry studies. A 2022 paper in Organic Letters described a novel catalytic method for its preparation, which reduces reaction time and improves yield compared to traditional approaches. This advancement not only streamlines the chemical synthesis process but also aligns with the principles of green chemistry by minimizing waste and energy consumption. Such innovations are critical for scaling up production in pharmaceutical manufacturing and industrial applications.

Moreover, N-Nitro-diphenylamine has shown promise in biomedical applications. Preliminary studies suggest its potential as a drug delivery agent due to its ability to interact with specific biological targets. Researchers are exploring its use in targeted drug delivery systems and nanocarriers for improved therapeutic outcomes. While further clinical trials are needed, these findings highlight the compound's potential to contribute to personalized medicine and precision healthcare.

In the realm of materials science, N-Nitro-diphenylamine has been studied for its role in conducting polymers. A 2021 review in Advanced Materials emphasized its utility in creating high-performance composites with enhanced mechanical and electrical properties. These materials are being explored for applications in smart textiles, biomedical implants, and electronic devices, showcasing the compound's broad applicability across multiple technical disciplines.

The environmental impact of N-Nitro-diphenylamine production is another area of active research. Scientists are focusing on eco-friendly synthesis methods to reduce the ecological footprint of its manufacturing. This aligns with the growing emphasis on sustainable development and resource efficiency in the chemical industry. Such efforts are crucial for ensuring that the benefits of N-Nitro-diphenylamine are realized without compromising environmental integrity.

As research into N-Nitro-diphenylamine continues to evolve, its role in innovative technologies and scientific advancements is becoming increasingly evident. From materials science to biomedical applications, the compound's unique properties offer opportunities for groundbreaking discoveries. Ongoing studies are likely to expand its potential uses, further solidifying its importance in the chemical sciences and related fields.

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