Cas no 101848-49-1 (1,4-Bis(4-Hydroxyphenoxy)Butane)
1,4-Bis(4-Hydroxyphenoxy)Butane Chemical and Physical Properties
Names and Identifiers
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- 1,4-Bis(4-Hydroxyphenoxy)Butane
- 4,4'-[1,4-Butanediylbis(oxy)]diphenol
- 1,4-benzenedibutanol
- 1,4-bis(4-hydroxybutyl)benzene
- 1,4-bis-(4-hydroxy-butyl)-benzene
- 1,4-Bis-(4-hydroxy-butyl)-benzol
- 1,4-bis-(4-hydroxyphenoxy)butane
- 4,4'-(1,4-phenylene)dibutan-1-ol
- 4,4'-(1,4-phenylene)dibutanol
- AC1NN59Q
- AC1Q7COX
- CTK0J7817
- SureCN242504
-
Computed Properties
- Exact Mass: 274.12054
Experimental Properties
- PSA: 58.92
1,4-Bis(4-Hydroxyphenoxy)Butane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B436078-10mg |
1,4-Bis(4-hydroxyphenoxy)butane |
101848-49-1 | 10mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B436078-50mg |
1,4-Bis(4-hydroxyphenoxy)butane |
101848-49-1 | 50mg |
$ 160.00 | 2022-06-07 | ||
| TRC | B436078-100mg |
1,4-Bis(4-hydroxyphenoxy)butane |
101848-49-1 | 100mg |
$ 250.00 | 2022-06-07 |
1,4-Bis(4-Hydroxyphenoxy)Butane Related Literature
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
Additional information on 1,4-Bis(4-Hydroxyphenoxy)Butane
1,4-Bis(4-Hydroxyphenoxy)Butane: A Comprehensive Overview
1,4-Bis(4-Hydroxyphenoxy)Butane (CAS No: 101848-49-1) is a versatile compound with a unique chemical structure that has garnered significant attention in various scientific and industrial applications. This compound, also referred to as bisphenol F derivative, is characterized by its two hydroxyl groups attached to the phenyl rings, which are further connected via ether linkages to a butane chain. Its molecular formula is C16H20O3, and it exhibits a melting point of approximately 75°C, making it suitable for a wide range of thermal applications.
The synthesis of 1,4-Bis(4-Hydroxyphenoxy)Butane involves a multi-step process that typically begins with the hydroxylation of phenol derivatives followed by etherification reactions. Recent advancements in catalytic systems have enabled more efficient and environmentally friendly production methods, reducing the overall carbon footprint associated with its manufacturing process. This compound's ability to form stable polymeric structures has made it a valuable precursor in the production of high-performance polymers and resins.
One of the most notable applications of 1,4-Bis(4-Hydroxyphenoxy)Butane is in the field of polymer science, where it serves as a key building block for synthesizing thermosetting resins and epoxy polymers. These materials are widely used in aerospace, automotive industries, and electronics due to their exceptional thermal stability and mechanical strength. Moreover, research has shown that this compound can be modified to enhance its compatibility with biodegradable materials, opening new avenues for sustainable polymer development.
In the realm of materials science, 1,4-Bis(4-Hydroxyphenoxy)Butane has been explored for its potential in creating advanced composites and nanomaterials. Its ability to form cross-linked networks at the nanoscale has led to innovations in lightweight materials for aerospace applications. Recent studies have demonstrated that incorporating this compound into graphene-based composites can significantly improve their electrical conductivity without compromising mechanical integrity.
The chemical structure of 1,4-Bis(4-Hydroxyphenoxy)Butane plays a pivotal role in its reactivity and functionality. The hydroxyl groups on the phenyl rings provide sites for further functionalization, enabling the creation of derivatives with tailored properties. For instance, esterification reactions can be employed to modify its surface chemistry, making it more amenable for biomedical applications such as drug delivery systems or tissue engineering scaffolds.
Recent research has also highlighted the potential of 1,4-Bis(4-Hydroxyphenoxy)Butane in the development of stimuli-responsive materials. By incorporating this compound into hydrogels or elastomers, scientists have created materials that can respond to external stimuli such as temperature or pH changes. These materials hold promise for applications in smart drug delivery systems and adaptive textiles.
In conclusion, 1,4-Bis(4-Hydroxyphenoxy)Butane (CAS No: 101848-49-1) is a multifaceted compound with a wide array of applications across diverse fields. Its unique chemical structure and versatile properties make it an invaluable component in modern material science and polymer engineering. As research continues to uncover new functionalities and applications for this compound, its role in advancing technological innovations is expected to grow significantly.
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