Cas no 142648-65-5 (2,2-Bis(4-hydroxyphenyl)propanol)

2,2-Bis(4-hydroxyphenyl)propanol is a bisphenol derivative characterized by its hydroxyl-functionalized aromatic structure. This compound serves as a versatile intermediate in organic synthesis, particularly in the production of epoxy resins, polycarbonates, and other high-performance polymers. Its bifunctional phenolic groups enable cross-linking reactions, enhancing thermal stability and mechanical properties in polymer matrices. The propanol moiety further provides reactivity for modifications, such as esterification or etherification, broadening its utility in specialty chemical applications. Due to its well-defined molecular structure, it offers consistent performance in formulations requiring precise stoichiometry. The compound is typically handled under controlled conditions to maintain purity and reactivity.
2,2-Bis(4-hydroxyphenyl)propanol structure
142648-65-5 structure
Product Name:2,2-Bis(4-hydroxyphenyl)propanol
CAS No:142648-65-5
MF:C15H16O3
MW:244.285744667053
CID:182036
Update Time:2025-08-05

2,2-Bis(4-hydroxyphenyl)propanol Chemical and Physical Properties

Names and Identifiers

    • Benzeneethanol,4-hydroxy-b-(4-hydroxyphenyl)-b-methyl-
    • 2,2-Bis(4-hydroxyphenyl)propanol
    • 4-[1-hydroxy-2-(4-hydroxyphenyl)propan-2-yl]phenol
    • 2,2-Bis(4-hydroxyphenyl)-1-propanol
    • AC1LCVF4
    • ACMC-1CHFF
    • CHEBI:33613
    • CTK4C3229
    • SureCN4231386
    • Inchi: 1S/C15H16O3/c1-15(10-16,11-2-6-13(17)7-3-11)12-4-8-14(18)9-5-12/h2-9,16-18H,10H2,1H3
    • InChI Key: HHOUSCIEKLBSGQ-UHFFFAOYSA-N
    • SMILES: OCC(C)(C1C=CC(=CC=1)O)C1C=CC(=CC=1)O

Computed Properties

  • Exact Mass: 244.10998

Experimental Properties

  • PSA: 60.69

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Additional information on 2,2-Bis(4-hydroxyphenyl)propanol

Introduction to 2,2-Bis(4-hydroxyphenyl)propanol (CAS No. 142648-65-5)

2,2-Bis(4-hydroxyphenyl)propanol, also known as bisphenol A (BPA) alcohol, is a compound with the CAS number 142648-65-5. This compound is a derivative of bisphenol A (BPA) and has gained significant attention in recent years due to its potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. This introduction aims to provide a comprehensive overview of 2,2-Bis(4-hydroxyphenyl)propanol, highlighting its chemical properties, synthesis methods, and recent research developments.

Chemical Structure and Properties

2,2-Bis(4-hydroxyphenyl)propanol is characterized by its unique molecular structure, which consists of two 4-hydroxyphenyl groups attached to a central propanol moiety. The molecular formula of this compound is C15H16O3, and it has a molecular weight of approximately 256.30 g/mol. The presence of hydroxyl groups imparts polarity to the molecule, making it soluble in polar solvents such as water and ethanol. Additionally, the aromatic rings contribute to the compound's stability and reactivity.

Synthesis Methods

The synthesis of 2,2-Bis(4-hydroxyphenyl)propanol can be achieved through several routes. One common method involves the reaction of bisphenol A with an appropriate alcohol in the presence of a catalyst. For instance, bisphenol A can be reacted with propanol in the presence of an acid catalyst such as sulfuric acid or p-toluenesulfonic acid. This reaction typically proceeds via nucleophilic substitution, leading to the formation of the desired product. Another approach involves the reduction of bisphenol A diacetate using a suitable reducing agent such as sodium borohydride or hydrogen gas over a palladium catalyst.

Applications in Pharmaceuticals

2,2-Bis(4-hydroxyphenyl)propanol has shown promise in pharmaceutical applications due to its potential biological activities. Recent studies have explored its use as an intermediate in the synthesis of various drugs and drug candidates. For example, it has been used as a building block in the development of anti-inflammatory agents and antioxidants. The hydroxyl groups in the molecule can participate in hydrogen bonding and other interactions that are crucial for biological activity.

Materials Science Applications

In materials science, 2,2-Bis(4-hydroxyphenyl)propanol has been investigated for its use in the preparation of advanced polymers and resins. Its ability to form stable networks through cross-linking reactions makes it a valuable monomer for producing high-performance materials. These materials exhibit excellent mechanical properties, thermal stability, and chemical resistance, making them suitable for applications in electronics, automotive industries, and construction.

Recent Research Developments

The scientific community continues to explore new avenues for utilizing 2,2-Bis(4-hydroxyphenyl)propanol. Recent research has focused on optimizing synthesis methods to improve yield and purity while reducing environmental impact. For instance, green chemistry approaches have been employed to develop more sustainable processes for producing this compound. Additionally, studies have investigated the potential health effects of exposure to bisphenol A derivatives, including 2,2-Bis(4-hydroxyphenyl)propanol. While concerns have been raised about the endocrine-disrupting properties of BPA, ongoing research aims to better understand these effects and develop safer alternatives.

Safety Considerations

Safety is a critical aspect when handling any chemical compound. While 2,2-Bis(4-hydroxyphenyl)propanol is not classified as a hazardous substance under current regulations, it is essential to follow standard laboratory safety protocols when working with this compound. Proper personal protective equipment (PPE), such as gloves and safety goggles, should be worn at all times. Additionally, appropriate ventilation should be ensured to minimize inhalation risks.

Conclusion

In conclusion, 2,2-Bis(4-hydroxyphenyl)propanol (CAS No. 142648-65-5) is a versatile compound with a wide range of applications in pharmaceuticals and materials science. Its unique chemical structure and properties make it an attractive candidate for various research and industrial uses. As research continues to advance our understanding of this compound's potential benefits and risks, it is likely that new applications will emerge in the coming years.

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