Cas no 4627-22-9 (Bis(4-tert-butylphenyl)amine)
Bis(4-tert-butylphenyl)amine Chemical and Physical Properties
Names and Identifiers
-
- Benzenamine,4-(1,1-dimethylethyl)-N-[4-(1,1-dimethylethyl)phenyl]-
- Bis(4-tert-butylphenyl)amine
- 4-(1,1-dimethylethyl)-N-[4-(1,1-dimethylethyl)phenyl]Benzenamine
- 4-tert-butyl-N-(4-tert-butylphenyl)aniline
- Bis(4-tert-butylphenyl)-amine
- 4,4'-Di-tert-butyldiphenylamine
- Bis(p-tert-butylphenyl)amine
- Di-4-tert-butylphenylamine
- N,N-Bis(4-tert-butylphenyl)amine
- Stearer STAR
- p,p'-Di-tert-butyldiphenylamine
- C20H27N
- CS-W009299
- 4627-22-9
- bis-(4-tert-butyl-phenyl)-amine
- DS-9511
- NCGC00328246-01
- N-NITROSO-4,4'-DI-TERT-BUTYLDIPHENYLAMINE
- SCHEMBL49741
- bis(4-t-butylphenyl)amine
- MFCD00417391
- DTXSID70332547
- Bis[4-(tert-butyl)phenyl]amine
- Q27288470
- S25750I14Y
- Benzenamine, 4-(1,1-dimethylethyl)-N-(4-(1,1-dimethylethyl)phenyl)-
- 4,4'-Di-tert-butyl-diphenylamine
- B2803
- AB01323711-02
- UNII-S25750I14Y
- AKOS005524091
- Benzenamine, 4-(1,1-dimethylethyl)-N-[4-(1,1-dimethylethyl)phenyl]-
- Oprea1_797667
- 4,4'-ditertiarybutyl-N,N-diphenylamine
- Bis(4-(tert-butyl)phenyl)amine
- 4,4'-di-t-butyldiphenylamine
- SY055185
- NS00076531
- DB-357298
- BBL036408
- STK721798
-
- MDL: MFCD00417391
- Inchi: 1S/C20H27N/c1-19(2,3)15-7-11-17(12-8-15)21-18-13-9-16(10-14-18)20(4,5)6/h7-14,21H,1-6H3
- InChI Key: OPEKHRGERHDLRK-UHFFFAOYSA-N
- SMILES: N(C1C=CC(=CC=1)C(C)(C)C)C1C=CC(=CC=1)C(C)(C)C
Computed Properties
- Exact Mass: 281.21400
- Monoisotopic Mass: 281.214349865g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 21
- Rotatable Bond Count: 4
- Complexity: 272
- 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: 6.8
- Topological Polar Surface Area: 12?2
Experimental Properties
- Color/Form: Uncertain
- Density: 0.974±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 105.0 to 109.0 deg-C
- Boiling Point: 195°C/3mmHg(lit.)
- Flash Point: 188.1°C
- Refractive Index: 1.552
- Solubility: Insuluble (1.6E-4 g/L) (25 oC),
- PSA: 12.03000
- LogP: 6.09820
- Solubility: Uncertain
Bis(4-tert-butylphenyl)amine Customs Data
- HS CODE:2921499090
- Customs Data:
China Customs Code:
2921499090Overview:
2921499090 Other aromatic monoamines and derivatives and their salts. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Bis(4-tert-butylphenyl)amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | B803634-100g |
Bis(4- |
4627-22-9 | 90% | 100g |
¥560.00 | 2022-09-02 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B2803-25g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90.0%(GC) | 25g |
¥300.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B2803-500g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90.0%(GC) | 500g |
¥1590.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B2803-100g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90.0%(GC) | 100g |
¥590.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | DX906-5g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90% | 5g |
¥64.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | DX906-25g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90% | 25g |
¥155.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | DX906-100g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90% | 100g |
¥510.0 | 2022-06-10 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R015921-100g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90% | 100g |
¥454 | 2024-05-23 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R015921-25g |
Bis(4-tert-butylphenyl)amine |
4627-22-9 | 90% | 25g |
¥137 | 2024-05-23 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | B803634-5g |
Bis(4- |
4627-22-9 | 90% | 5g |
¥53.00 | 2022-09-02 |
Bis(4-tert-butylphenyl)amine Suppliers
Bis(4-tert-butylphenyl)amine Related Literature
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Guang-Zhao Lu,Xiaokang Li,Liang Liu,Liang Zhou,You-Xuan Zheng,Wen-Wei Zhang,Jing-Lin Zuo,Hongjie Zhang J. Mater. Chem. C 2019 7 3862
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Si Hyun Han,Jae Ho Jeong,Ji Woong Yoo,Jun Yeob Lee J. Mater. Chem. C 2019 7 3082
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Guang-Zhao Lu,Ruixia Wu,Liang Liu,Liang Zhou,You-Xuan Zheng,Wen-Wei Zhang,Jing-Lin Zuo,Hongjie Zhang Mater. Chem. Front. 2019 3 860
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Bei Jiang,Yu Gu,Jingjing Qin,Xiaowen Ning,Shaolong Gong,Guohua Xie,Chuluo Yang J. Mater. Chem. C 2016 4 3492
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Huifang Yang,Zhiyuan Fu,Sai Wang,Haichao Liu,Jianwei Zhou,Kai Wang,Xiugang Wu,Bing Yang,Bo Zou,Weiguo Zhu Mater. Adv. 2021 2 4859
Additional information on Bis(4-tert-butylphenyl)amine
Introduction to Bis(4-tert-butylphenyl)amine (CAS No. 4627-22-9)
Bis(4-tert-butylphenyl)amine, with the chemical formula C26H35N and the CAS number 4627-22-9, is a significant compound in the field of chemical and pharmaceutical research. This organophosphorus compound has garnered considerable attention due to its unique structural properties and versatile applications in various scientific domains.
The molecular structure of Bis(4-tert-butylphenyl)amine consists of two 4-tert-butylphenyl groups bonded to a central amine nitrogen atom. This configuration imparts exceptional stability and reactivity, making it a valuable intermediate in the synthesis of complex molecules. The presence of bulky tert-butyl groups enhances steric hindrance, which can be strategically exploited in catalytic processes and material science applications.
In recent years, researchers have explored the potential of Bis(4-tert-butylphenyl)amine in the development of advanced materials, particularly in organic electronics. Its ability to act as a ligand in transition metal catalysis has been leveraged to design novel catalysts for cross-coupling reactions, which are pivotal in pharmaceutical synthesis. The compound's electron-donating nature and steric bulk make it an ideal candidate for tuning the electronic properties of organic semiconductors.
One of the most intriguing applications of Bis(4-tert-butylphenyl)amine is in the field of photovoltaics. Studies have demonstrated its efficacy as a hole-transporting material (HTM) in perovskite solar cells. The compound's high solubility and thermal stability allow for efficient charge transport, significantly improving the performance of solar cell devices. Recent advancements in this area have shown that optimizing the concentration and morphology of Bis(4-tert-butylphenyl)amine can lead to unprecedented efficiencies in photovoltaic devices.
The pharmaceutical industry has also benefited from the unique properties of Bis(4-tert-butylphenyl)amine. Its structural motif is reminiscent of many bioactive molecules, suggesting potential applications as a pharmacophore. Researchers have investigated its role as a modulator in enzyme inhibition studies, particularly targeting metalloproteinases involved in inflammatory pathways. Preliminary findings indicate that derivatives of this compound exhibit promising inhibitory activity, opening new avenues for drug discovery.
Furthermore, the compound's stability under various environmental conditions makes it suitable for industrial applications. It has been tested as a stabilizer in polymer formulations, enhancing thermal and oxidative resistance. This property is particularly valuable in high-performance plastics used in automotive and aerospace industries, where durability is paramount.
The synthesis of Bis(4-tert-butylphenyl)amine involves multi-step organic reactions, typically starting from commercially available aromatic precursors. The process requires precise control over reaction conditions to ensure high yield and purity. Advances in catalytic methods have streamlined this synthesis, making it more efficient and environmentally friendly. Techniques such as flow chemistry have been employed to optimize production scalability while minimizing waste.
In conclusion, Bis(4-tert-butylphenyl)amine (CAS No. 4627-22-9) is a multifaceted compound with broad applications across multiple scientific disciplines. Its role in organic electronics, photovoltaics, pharmaceuticals, and materials science underscores its importance as a research tool and industrial material. As research continues to uncover new functionalities and applications, the significance of this compound is expected to grow further.
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