Skip to main content

Bisphenol A

ADVERTISEMENT
Identification
Molecular formula
C15H14O2
CAS number
80-05-7
IUPAC name
4-(4-hydroxyphenyl)phenol
State
State

At room temperature, Bisphenol A is typically found as a solid, crystalline powder.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
228.29g/mol
Molar mass
228.2910g/mol
Density
1.1950g/cm3
Appearence

Bisphenol A typically appears as a white solid in crystalline form. It has a shiny, crystalline texture and tends to be available in both powder and pellet forms for industrial purposes.

Comment on solubility

Solubility of 4-(4-hydroxyphenyl)phenol

4-(4-hydroxyphenyl)phenol, often known as a biphenolic compound, exhibits interesting solubility properties that can vary depending on several factors. Here are some key insights regarding its solubility:

  • Solvent Compatibility: This compound is generally more soluble in organic solvents, such as ethanol and acetone, compared to polar solvents like water.
  • Hydrogen Bonding: The presence of the hydroxyl (-OH) group enables the compound to engage in hydrogen bonding, which enhances its solubility in polar organic solvents.
  • Temperature Dependence: Increased temperature often leads to a higher solubility, making it more soluble in hot solvents.
  • pH Influence: The solubility can be affected by the pH of the solution; in alkaline conditions, the solubility may increase due to deprotonation of the -OH group.

To summarize, while 4-(4-hydroxyphenyl)phenol is not highly soluble in water, it finds better solubility in a variety of organic solvents. This characteristic is pivotal in applications where organic solvent-based solutions are utilized.

Interesting facts

4-(4-Hydroxyphenyl)phenol: A Unique Compound

4-(4-Hydroxyphenyl)phenol, often referred to as a derivative of bisphenol, is an intriguing compound that has garnered attention in various fields including materials science, biochemistry, and even pharmacology. Here are some fascinating aspects:

  • Antioxidant Properties: This compound is known for its antioxidant capabilities. Antioxidants play a crucial role in mitigating oxidative stress in biological systems, which is linked to numerous diseases.
  • Application in Polymer Science: 4-(4-Hydroxyphenyl)phenol is utilized in the synthesis of polyphenylene oxide, a polymer renowned for its thermal stability and electrical insulating properties. This makes it valuable in industries ranging from electronics to automotive.
  • Potential Health Benefits: Research has indicated that compounds like 4-(4-hydroxyphenyl)phenol may possess anti-inflammatory properties. This opens pathways for future research into its applications in health and disease management.
  • Environmental Impact: As a phenolic compound, it’s crucial to consider its biodegradability and environmental footprint. Understanding such properties is essential for sustainable development.
  • Intermolecular Interactions: The structure of 4-(4-Hydroxyphenyl)phenol allows it to engage in interesting hydrogen bonding and π-π interactions, influencing solubility and reactivity.

Moreover, the versatility of this compound highlights the importance of phenolic derivatives in both synthetic and natural processes. As emphasized by researchers, "the study of phenolic compounds is vital in understanding numerous biochemical pathways." This showcases the continuous relevance of compounds like 4-(4-hydroxyphenyl)phenol in advancing both scientific knowledge and practical applications.

Overall, 4-(4-hydroxyphenyl)phenol stands out as a compound with potential implications that reach beyond just its structural formula, representing a bridge between organic chemistry and real-world applications.

Synonyms
4,4'-Dihydroxybiphenyl
92-88-6
4,4'-BIPHENOL
4,4'-Biphenyldiol
Biphenyl-4,4'-diol
[1,1'-Biphenyl]-4,4'-diol
p,p'-Biphenol
p,p'-Diphenol
4,4'-dihydroxydiphenyl
Antioxidant DOD
4,4'-Dioxydiphenyl
4,4'-Diphenol
p-Dihydroxydiphenyl
4,4'-Bisphenol
p,p'-Dihydroxybiphenyl
4-(4-hydroxyphenyl)phenol
para,para'-Biphenol
ASM DOD
4,4'-Dioxydiphenol
USAF DO-30
4,4-Biphenol
(1,1'-Biphenyl)-4,4'-diol
Phenol p-(p-hydroxyphenyl)-
4,4'-Dihydroxy-1,1'-biphenyl
NSC 8711
DOD
CCRIS 2981
Dihydroxybiphenyl
4,4'-Dihydroxy-biphenyl
EINECS 202-200-5
4,4'biphenol
BRN 1908886
DTXSID1029120
CHEBI:34367
4,4'-Hydroxybiphenyl
AI3-16055
4,4`-dihydroxybiphenyl
NSC-8711
MFCD00002348
CHEMBL76398
DTXCID709120
GM-W06
GM-W07
R8994A0904
EC 202-200-5
4-06-00-06651 (Beilstein Handbook Reference)
4,4'-DIHYDROXYDIPHENYL-D8 (RINGS-D8)
4,4'-diphenyldiol
44'BP cpd
p,p'Biphenol
p,p'Diphenol
pDihydroxydiphenyl
4,4'biphenyldiol
p,p''-biphenol
para,para'Biphenol
UNII-R8994A0904
Biphenyl4,4'diol
4,4-dioxydiphenyl
4,4'Bisphenol
4,4'Dioxydiphenyl
4,4'Diphenol
p,p'Dihydroxybiphenyl
4,4''-biphenol
4,4''-Biphenyldiol
4,4''-dioxydiphenyl
4,4'Dihydroxydiphenyl
4,4'-Dihydroxybipheny
biphenyl-4,4''-diol
biphenyl-4,4\'-diol
p,p''-dihydroxybiphenyl
4(4Hydroxyphenyl)phenol
Phenol p(phydroxyphenyl)
4,4''-Dihydroxybiphenyl
4,4'-Dihydroxy biphenyl
WLN: QR DR DQ
4,4'-bis-hydroxybiphenyl
[1,4'-diol
Oprea1_514666
SCHEMBL15632
(1,1'Biphenyl)4,4'diol
BIDD:ER0226
1,1'-biphenyl-4,4'-diol
Phenol, p-(p-hydroxyphenyl)-
4,4'-Dihydroxybiphenyl, 97%
4,4'-Dihydroxydiphenyl (DOD)
NSC8711
Tox21_200469
[1,1''-biphenyl]-4,4''-diol
BDBM50121958
STK365601
AKOS005442497
AC-7327
CS-W016905
FD10896
HY-W016189
CAS-92-88-6
NCGC00248640-01
NCGC00248640-02
NCGC00258023-01
AS-14303
B0464
NS00002875
D77801
AB01334799-02
EN300-4290281
Q2168450
4,4'-Dihydroxybiphenyl, Vetec(TM) reagent grade, 97%
F0001-2226
Z1255423443
202-200-5
4HB