Cas no 78600-33-6 (3-Bromotriphenylamine)
3-Bromotriphenylamine Chemical and Physical Properties
Names and Identifiers
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- Benzenamine,3-bromo-N,N-diphenyl-
- 3-Bromo Triphenylamine
- 3-Bromo-N,N-diphenylaniline
- 3-bromo-N,N-diphenylBenzenamine
- 3-Bromotriphenylamine
- 3-Bromo-N,N-diphenylaniline;Benzenamine, 3-romo-,-iphenyl-
- N,N-Diphenyl-3-bromoaniline
- 3-bromo-N,N-diphenyl-aniline
- YDXLVFKTOSKBKT-UHFFFAOYSA-N
- Benzenamine, 3-bromo-N,N-diphenyl-
- N-(3-bromophenyl)-N,N-diphenylamine
- DTXSID80584595
- 3-BROMO-N N-DIPHENYLANILINE 97
- A852008
- 78600-33-6
- 3-Bromo-N,N-diphenylaniline, 97%
- C16378
- 3-bromo-n n-diphenylaniline
- CS-W013944
- FT-0718618
- 3-Bromo-N,N-diphenylaniline;Benzenamine, 3-bromo-N,N-diphenyl-
- SCHEMBL4890429
- AKOS025295759
- AS-59118
- B4036
- MFCD06798123
- DB-075496
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- MDL: MFCD06798123
- Inchi: 1S/C18H14BrN/c19-15-8-7-13-18(14-15)20(16-9-3-1-4-10-16)17-11-5-2-6-12-17/h1-14H
- InChI Key: YDXLVFKTOSKBKT-UHFFFAOYSA-N
- SMILES: BrC1=CC=CC(=C1)N(C1C=CC=CC=1)C1C=CC=CC=1
Computed Properties
- Exact Mass: 323.03100
- Monoisotopic Mass: 323.03096g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 20
- Rotatable Bond Count: 3
- Complexity: 263
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 5.9
- Topological Polar Surface Area: 3.2
Experimental Properties
- Color/Form: No data available
- Density: 1.369±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 90.0 to 94.0 deg-C
- Boiling Point: 193°C/2.5mmHg(lit.)
- Flash Point: 207.2±24.0 °C
- Refractive Index: 1.664
- Solubility: Insuluble (2.5E-4 g/L) (25 oC),
- PSA: 3.24000
- LogP: 5.91890
3-Bromotriphenylamine Security Information
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Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H302-H315-H317-H319-H335-H413
- Warning Statement: P261-P280-P305 + P351 + P338
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 22-36/37/38
- Safety Instruction: S26; S36/37/39
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Hazardous Material Identification:
- Safety Term:26-36/37/39
- Risk Phrases:R22; R36/37/38
- Storage Condition:Store at 4°C,-4At ℃Store…Better
3-Bromotriphenylamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B134545-1g |
3-Bromotriphenylamine |
78600-33-6 | >98.0% | 1g |
¥91.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B134545-25g |
3-Bromotriphenylamine |
78600-33-6 | >98.0% | 25g |
¥1202.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B134545-5g |
3-Bromotriphenylamine |
78600-33-6 | >98.0% | 5g |
¥372.90 | 2023-09-04 | |
| Alichem | A019116690-5g |
3-Bromo-N,N-diphenylaniline |
78600-33-6 | 95% | 5g |
$183.75 | 2023-09-01 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R013519-1g |
3-Bromotriphenylamine |
78600-33-6 | 97% | 1g |
¥58 | 2024-05-21 | |
| TRC | B687968-50mg |
3-Bromotriphenylamine |
78600-33-6 | 50mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B687968-100mg |
3-Bromotriphenylamine |
78600-33-6 | 100mg |
$ 65.00 | 2022-06-06 | ||
| TRC | B687968-500mg |
3-Bromotriphenylamine |
78600-33-6 | 500mg |
$ 135.00 | 2022-06-06 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | B834747-5g |
3-Bromotriphenylamine |
78600-33-6 | 97% | 5g |
¥388.00 | 2022-09-02 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 647527-1G |
3-Bromotriphenylamine |
78600-33-6 | 97% | 1G |
¥503.48 | 2022-02-24 |
3-Bromotriphenylamine Suppliers
3-Bromotriphenylamine Related Literature
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Felix Witte,Philipp Rietsch,Nithiya Nirmalananthan-Budau,Florian Weigert,Jan P. G?tze,Ute Resch-Genger,Siegfried Eigler,Beate Paulus Phys. Chem. Chem. Phys., 2021,23, 17521-17529
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Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099
Additional information on 3-Bromotriphenylamine
3-Bromotriphenylamine (CAS 78600-33-6): Properties, Applications, and Market Insights
3-Bromotriphenylamine (CAS 78600-33-6) is an important organic compound belonging to the class of triphenylamine derivatives. This brominated aromatic amine has gained significant attention in recent years due to its versatile applications in organic electronics, photovoltaic materials, and advanced material science. With the growing interest in sustainable energy solutions and next-generation display technologies, compounds like 3-Bromotriphenylamine are becoming increasingly valuable in both research and industrial applications.
The molecular structure of 3-Bromotriphenylamine features a central nitrogen atom connected to three phenyl rings, with one of the rings substituted by a bromine atom at the meta position. This specific substitution pattern contributes to its unique electronic properties and makes it particularly useful as a building block for more complex molecular architectures. Researchers are particularly interested in how the bromine substituent affects the compound's charge transport properties and photophysical characteristics, which are crucial for applications in OLED technology and organic photovoltaics.
In the field of organic light-emitting diodes (OLEDs), 3-Bromotriphenylamine serves as an important hole-transport material. Its ability to facilitate efficient charge transport while maintaining good thermal stability makes it valuable for developing energy-efficient displays and lighting solutions. With the global push toward eco-friendly technologies and the phasing out of traditional lighting, the demand for high-performance OLED materials continues to grow, positioning 3-Bromotriphenylamine as a compound of significant commercial interest.
The compound also finds applications in organic photovoltaics, where it can be used as a donor material or as part of more complex molecular architectures for solar cell applications. As the world shifts toward renewable energy sources, research into more efficient organic solar cells has intensified, with compounds like 3-Bromotriphenylamine playing a role in developing next-generation photovoltaic materials that offer improved efficiency and lower production costs compared to traditional silicon-based technologies.
From a synthetic chemistry perspective, 3-Bromotriphenylamine serves as a valuable intermediate for the preparation of various functional materials. The bromine atom provides an excellent reactive site for further functionalization through cross-coupling reactions, allowing chemists to create more complex structures with tailored properties. This versatility makes it particularly useful in materials science research and the development of specialty chemicals for advanced applications.
The global market for triphenylamine derivatives has been expanding steadily, driven by increasing demand from the electronics industry and energy sector. As a specialized derivative, 3-Bromotriphenylamine occupies a niche but growing segment of this market. Manufacturers and suppliers are focusing on developing more efficient synthesis routes to meet the rising demand while maintaining high purity standards required for electronic-grade materials.
Recent advancements in green chemistry have also impacted the production and application of 3-Bromotriphenylamine. Researchers are exploring more sustainable synthesis methods and investigating its potential in biodegradable electronic devices, aligning with the broader trend toward environmentally friendly technologies. These developments are particularly relevant as industries face increasing pressure to adopt sustainable practices throughout their supply chains.
Quality control and characterization of 3-Bromotriphenylamine are critical aspects of its production and application. Advanced analytical techniques such as HPLC, NMR spectroscopy, and mass spectrometry are routinely employed to ensure product purity and consistency. For applications in electronic devices, even trace impurities can significantly affect performance, making rigorous quality control essential for manufacturers serving this market.
Looking to the future, 3-Bromotriphenylamine is expected to play an increasingly important role in the development of flexible electronics and wearable technologies. Its combination of good charge transport properties and synthetic versatility makes it a promising candidate for these emerging applications. As research continues into organic electronic materials, we can anticipate new discoveries that will further expand the potential uses of this interesting compound.
For researchers and industry professionals working with 3-Bromotriphenylamine, staying informed about the latest developments in synthesis methods, applications, and safety considerations is essential. The compound's unique properties and growing range of applications ensure that it will remain an important material in the toolkit of materials scientists and organic chemists working at the forefront of technology development.
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