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Bisphenol A

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Identification
Molecular formula
C15H16O
CAS number
80-05-7
IUPAC name
4-(1-methyl-1-phenyl-ethyl)phenol
State
State

At room temperature, Bisphenol A is in a solid state. It is most commonly encountered in the form of powder or flakes.

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 appears as white to off-white crystalline flakes or a powder. It is relatively colorless and presents itself as a solid under normal conditions. The substance may also occasionally appear in granular form.

Comment on solubility

Solubility of 4-(1-methyl-1-phenyl-ethyl)phenol

4-(1-methyl-1-phenyl-ethyl)phenol, also known as a substituted phenolic compound, exhibits unique solubility characteristics that depend on several factors. This compound is generally found to be:

  • Moderately soluble in organic solvents: Its lipophilic (water-repelling) characteristics make it dissolve well in solvents such as ethanol, methanol, and acetone.
  • Poorly soluble in water: As a phenolic compound, it has limited solubility in aqueous solutions, which is a common feature among many organic molecules containing long hydrophobic alkyl chains.

Furthermore, the solubility can be influenced by:

  • Temperature: An increase in temperature generally enhances the solubility of organic compounds.
  • pH levels: The degree of ionization of the phenol group can vary with pH, potentially affecting its solubility in water.

In conclusion, the solubility of 4-(1-methyl-1-phenyl-ethyl)phenol is significantly impacted by its molecular structure, with its **phenolic group** contributing to greater solubility in organic solvents while restricting its interaction with water. This dual nature highlights the intriguing balance between hydrophilic and hydrophobic interactions in compound behavior.

Interesting facts

Interesting Facts About 4-(1-methyl-1-phenyl-ethyl)phenol

4-(1-methyl-1-phenyl-ethyl)phenol, commonly referred to in scientific circles as a member of the phenolic family, possesses a fascinating chemical structure that contributes richly to its chemical behavior and potential applications.

Chemical Structure and Properties

This compound features a unique configuration where a phenolic group is substituted. Notably, the branched alkyl chain attached to the phenol ring plays a significant role in its reactivity and solubility characteristics. Such substituents can influence the compound's ability to participate in chemical reactions, as the spatial arrangement of atoms can affect aspect such as sterics and electronic distribution.

Applications and Uses

The properties of 4-(1-methyl-1-phenyl-ethyl)phenol make it a valuable candidate for various applications, including:

  • Pharmaceuticals: It can serve as a precursor for the synthesis of biologically active compounds.
  • Antioxidant Agent: Some studies suggest that it may exhibit antioxidant properties, making it relevant in formulations aimed at reducing oxidative stress.
  • Industrial Chemicals: Its unique structure allows for potential use in products ranging from plastics to coatings.

Environmental Considerations

As with many organic compounds, research is ongoing into the environmental impacts of 4-(1-methyl-1-phenyl-ethyl)phenol. Understanding degradation pathways and toxicity levels is essential for ensuring safe handling and usage.

In Summary

4-(1-methyl-1-phenyl-ethyl)phenol is an intriguing compound that showcases the complexity of organic chemistry. Its multifaceted applications and the necessity for responsible environmental management highlight the dual nature of such compounds: they can solve problems while also presenting challenges. As noted by researchers, "The exploration of phenolic compounds continues to unveil new opportunities and insights into their role in modern science."


Synonyms
4-Cumylphenol
599-64-4
p-Cumylphenol
4-(2-phenylpropan-2-yl)phenol
4-alpha-Cumylphenol
Phenol, 4-(1-methyl-1-phenylethyl)-
4-(1-Methyl-1-phenylethyl)phenol
p-Cumyl phenol
4-(Dimethylphenylmethyl)phenol
4-Hydroxydiphenyldimethylmethane
2-Phenyl-2-(4-hydroxyphenyl)propane
p-(alpha-Cumenyl)phenol
2-Phenyl-2-(p-hydroxyphenyl)propane
p-(.alpha.-Cumyl)phenol
NSC 6237
p-(alpha,alpha-Dimethylbenzyl)phenol
4-(alpha,alpha-Dimethylbenzyl)phenol
Phenol, 4-(1-methyl-1-phenethyl)-
4-(1-Methyl-1-phenethyl)phenol
2RLA3OL3QT
EINECS 209-968-0
Phenol, p-(.alpha.,.alpha.-dimethylbenzyl)-
BRN 1870517
CCRIS 8908
DTXSID3022536
4-(.alpha.,.alpha.-Dimethylbenzyl)phenol
p-(.alpha.,.alpha.-Dimethylbenzyl)phenol
AI3-08269
HSDB 8089
NSC-6237
Phenol, p-(alpha,alpha-dimethylbenzyl)-
4-.ALPHA.-CUMYLPHENOL
DTXCID502536
EC 209-968-0
PHENYLISOPROPYL)PHENOL, 4-(2-
2-(4-HYDROXYPHENYL)-2-PHENYLPROPANE
p-[alpha,alpha-dimethylbenzyl)phenol
pCumyl phenol
4Cumylphenol
p(alphaCumenyl)phenol
p(alphaCumyl) phenol
p-(alpha-Cumyl)phenol
p-(alpha-cumyl) phenol
4(1Methyl1phenethyl)phenol
4(1Methyl1phenylethyl)phenol
4(Dimethylphenylmethyl)phenol
4Hydroxydiphenyldimethylmethane
Phenol, 4(1methyl1phenethyl)
2Phenyl2(phydroxyphenyl)propane
2Phenyl2(4hydroxyphenyl)propane
4-(dimethylphenylmethyl) phenol
Phenol, 4(1methyl1phenylethyl)
p(alpha,alphaDimethylbenzyl)phenol
4(alpha,alphaDimethylbenzyl)phenol
4-(1-methyl-1-phenethyl)-9CI
Phenol, p(alpha,alphadimethylbenzyl)
p-(alpha-alpha-dimethylbenzyl) phenol
Phenol, 4(1methyl1phenethyl) (9CI)
phenol, p-(alpha-alpha-dimethyl-benzyl)
Phenol, 4-(1-methyl-1-phenethyl)-(9CI)
209-968-0
4-(2-PHENYLISOPROPYL)PHENOL
MFCD00002365
paracumylphenol
CHEBI:35092
CAS-599-64-4
UNII-2RLA3OL3QT
p-Hydroxy-2,2-diphenylpropane
para-cumylphenol
p--cumylphenol
2zas
4-|A-Cumylphenol
4-Cumylphenol, 99%
Cambridge id 5142949
p-(.alpha.-Cumenyl)phenol
TimTec1_002380
p-(2-Phenylisopropyl)phenol
SCHEMBL51117
BIDD:ER0173
4-(2-Phenylisopropyl) phenol
[1, ar'-(1-methylethyl)-
CHEMBL194805
BDBM29609
Phenol,.alpha.-dimethylbenzyl)-
NSC6237
HMS1540M04
HMS3604L17
KUC105982N
AAA59964
Tox21_201297
Tox21_300056
4-(1-Methyl-1-phenylethyl)-phenol
STK831902
4-(1-Methyl-1-phenyl-ethyl)-phenol
AKOS000120751
2-(4'-Hydroxyphenyl)-2-phenylpropane
CS-W014998
DB06902
HY-W014282
KSC-19-030
NCGC00090941-01
NCGC00090941-02
NCGC00090941-03
NCGC00090941-04
NCGC00090941-05
NCGC00253961-01
NCGC00258849-01
AS-57116
SY049300
DB-072734
NS00009362
EN300-17891
E83013
BRD-K94049994-001-01-5
Q27095806
Z57068819
F0020-1559
2-(4'-Hydroxyphenyl)-2-phenylpropane; 4-alpha-Cumylphenol
1OH