• 1. Photoinduced electron transfer at liquid/liquid interfaces Part II. A study of the electron transfer and recombination dynamics by intensity modulated photocurrent spectroscopy (IMPS)
  David J. Fermín,H Dung Duong,Zhifeng Ding,ois Brevet,Hubert H. Girault Phys. Chem. Chem. Phys. 1999 1 1461
• 2. Generation of a triplet diradical from a donor–acceptor cross conjugate upon acid-induced electron transfer
  Mats O. Sandberg,Osami Nagao,Zhikun Wu,Michio M. Matsushita,Tadashi Sugawara Chem. Commun. 2008 3738
• 3. Generation of a triplet diradical from a donor–acceptor cross conjugate upon acid-induced electron transfer
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Tertiary amines

Comprehensive Guide to Tris(4-methoxyphenyl)amine (CAS No. 13050-56-1): Properties, Applications, and Market Insights

Tris(4-methoxyphenyl)amine (CAS No. 13050-56-1) is a specialized organic compound widely recognized for its unique chemical structure and versatile applications in advanced materials. This triarylamine derivative features three methoxy-substituted phenyl groups attached to a central nitrogen atom, making it an excellent candidate for organic electronics and photovoltaic research. Its molecular formula, C₂₁H₂₁NO₃, and molecular weight of 335.40 g/mol contribute to its stability and solubility in organic solvents.

The compound's electron-donating properties and hole-transport capabilities have made it a subject of interest in the development of OLEDs (Organic Light-Emitting Diodes) and solar cells. Researchers frequently search for "Tris(4-methoxyphenyl)amine synthesis" or "13050-56-1 applications in optoelectronics," highlighting its relevance in cutting-edge technologies. Recent studies have explored its potential in perovskite solar cells, where it enhances charge transport and device efficiency.

In addition to optoelectronic applications, Tris(4-methoxyphenyl)amine serves as a key intermediate in pharmaceutical research and material science. Its methoxy groups improve solubility and processability, making it suitable for thin-film deposition techniques. The compound's thermal stability (decomposition temperature >300°C) further supports its use in high-performance materials. Industry professionals often inquire about "buy Tris(4-methoxyphenyl)amine" or "CAS 13050-56-1 suppliers," reflecting growing commercial demand.

The global market for triarylamine derivatives like Tris(4-methoxyphenyl)amine is expanding, driven by advancements in renewable energy technologies and flexible electronics. Environmental concerns and the push for sustainable materials have increased interest in this compound's eco-friendly applications. Analytical techniques such as HPLC, NMR, and mass spectrometry are commonly employed to verify its purity and structural integrity.

Safety data for CAS 13050-56-1 indicates standard handling precautions for laboratory chemicals, including the use of personal protective equipment (PPE). While not classified as hazardous under major regulatory frameworks, proper storage conditions (e.g., away from strong oxidizers) are recommended. Researchers exploring "Tris(4-methoxyphenyl)amine safety profile" will find comprehensive MSDS documentation available from reputable suppliers.

Future research directions for Tris(4-methoxyphenyl)amine may focus on its nanostructured forms and composite materials, particularly for energy storage systems. The compound's compatibility with printing technologies positions it as a promising material for large-area electronics manufacturing. With increasing patent filings related to 13050-56-1 derivatives, intellectual property considerations are becoming crucial for commercial applications.

For laboratories and industries working with triarylamine compounds, proper characterization of Tris(4-methoxyphenyl)amine includes monitoring its optical bandgap (typically 3.1-3.4 eV) and electrochemical properties. These parameters significantly influence performance in optoelectronic devices. Recent publications have demonstrated its effectiveness as a host material in phosphorescent OLEDs, achieving improved luminance efficiency.

The synthesis of Tris(4-methoxyphenyl)amine typically involves Ullmann-type coupling reactions or Buchwald-Hartwig amination, with yields optimized through catalyst selection. Process chemists frequently search for "13050-56-1 synthesis optimization" to improve cost-efficiency for industrial-scale production. Green chemistry approaches using palladium-free catalysts represent an active area of development.

In academic settings, CAS 13050-56-1 serves as a valuable model compound for studying charge transfer mechanisms in organic semiconductors. Its well-defined redox behavior makes it suitable for teaching advanced concepts in materials chemistry. Educational suppliers often list it among essential compounds for graduate-level research in functional materials.

Quality control protocols for Tris(4-methoxyphenyl)amine emphasize the importance of residual solvent analysis and metal impurity testing, particularly for electronic-grade material. The compound's performance in devices correlates strongly with purity levels (>99.5% preferred). Industry standards continue to evolve regarding 13050-56-1 specifications for different application tiers.

Emerging applications in bioelectronics and neural interfaces have created new research avenues for triarylamine-based materials. The compound's biocompatibility profile and tunable electronic properties show promise for next-generation medical devices. Cross-disciplinary collaborations are exploring its potential in wearable sensors and implantable electronics.

Market analysts project steady growth for Tris(4-methoxyphenyl)amine demand, particularly in Asia-Pacific regions with strong electronics manufacturing sectors. Price trends reflect fluctuations in methoxybenzene precursor availability and specialty chemical market dynamics. Strategic partnerships between academic researchers and industrial manufacturers are accelerating technology transfer.

Environmental impact assessments of CAS 13050-56-1 production processes focus on solvent recovery systems and waste minimization strategies. The compound's low ecotoxicity profile supports its selection over alternative materials in green electronics initiatives. Regulatory compliance remains straightforward for most international markets.

Recent innovations include nanoparticulate formulations of Tris(4-methoxyphenyl)amine for inkjet-printed electronics, demonstrating superior film-forming characteristics. Patent literature reveals growing interest in its coordination complexes with transition metals for catalytic applications. These developments position 13050-56-1 as a multifaceted compound with expanding technological relevance.

For researchers entering this field, key reference works include studies on triarylamine molecular design and structure-property relationships. The compound's crystallographic data and spectroscopic signatures are well-documented in chemical databases. Open-access publications have increased visibility of Tris(4-methoxyphenyl)amine research findings across global scientific communities.

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• 105653-70-1(Benzenamine, 4,4'-oxybis[N-methyl-N-phenyl-)
• 27151-57-1(Benzenamine,4-methoxy-N-(4-methoxyphenyl)-N-methyl-)
• 54480-44-3(1,4-Benzenediamine, N'-(4-methoxyphenyl)-N,N-dimethyl-)
• 106614-60-2(Benzenamine, 3-methoxy-N,N-bis(3-methoxyphenyl)-)
• 20440-94-2(4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline)
• 4316-51-2(4-Methoxytriphenylamine)
• 54263-65-9(Benzenamine, 3-methoxy-N-methyl-N-phenyl-)
• 55251-46-2(4-Methoxy-N-methyl-N-phenylaniline)
• 109462-63-7(1,4-Benzenediamine, N-(4-methoxyphenyl)-N,N'-dimethyl-N'-phenyl-)