Skip to main content

Bisphenol S

ADVERTISEMENT
Identification
Molecular formula
C12H10O4S
CAS number
80-09-1
IUPAC name
4-(4-hydroxyphenyl)sulfonylphenol
State
State

Bisphenol S is typically found in a solid state at room temperature. Due to its crystalline structure, it is stable at room temperature and does not vaporize easily.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.15
Boiling point (Celsius)
592.30
Boiling point (Kelvin)
865.45
General information
Molecular weight
250.27g/mol
Molar mass
250.2730g/mol
Density
1.3660g/cm3
Appearence

Bisphenol S appears as a white crystalline solid. It can also appear in powder form with a slight beige or off-white coloration.

Comment on solubility

Solubility Characteristics of 4-(4-hydroxyphenyl)sulfonylphenol

4-(4-hydroxyphenyl)sulfonylphenol, with its complex structure, exhibits unique solubility behavior, which is essential for its applications in various chemical processes. The solubility of this compound depends on several factors, including:

  • Temperature: As with many organic compounds, increasing the temperature typically enhances solubility.
  • Solvent Choice: The choice of solvent plays a crucial role; polar solvents like water may dissolve certain functionalities, while non-polar solvents may not engage effectively with its sulfonyl group.
  • pH of Solution: The presence of hydroxyl groups can affect solubility in aqueous solutions, as the acid-base properties can lead to protonation or deprotonation, influencing solubility.

In general, compounds with sulfonyl groups are known for their increased solubility in polar solvents due to their ability to form hydrogen bonds. However, the presence of multiple aromatic rings in 4-(4-hydroxyphenyl)sulfonylphenol may decrease solubility due to increased hydrophobic interactions. It is often noted that:

"Hydrophobic segments tend to limit solubility in polar solvents, while polar functional groups can enhance interactions with water molecules."

This compound may find limited solubility in water, while being more soluble in organic solvents that are capable of stabilizing its aromatic and polar character. This nuanced perspective on solubility is vital for understanding its behavior in various chemical processes.

Interesting facts

Interesting Facts about 4-(4-hydroxyphenyl)sulfonylphenol

4-(4-hydroxyphenyl)sulfonylphenol, often referred to within scientific circles as a thought-provoking compound, has a rich background and various applications that make it noteworthy. Here are some key points that highlight its significance:

  • Chemical Structure: This compound features a sulfonyl group, which plays a crucial role in its reactivity and interaction with other molecules. The presence of hydroxyl groups enhances its solubility in various solvents.
  • Applications in Medicine: Research shows that derivatives of this compound have potential uses in the pharmaceutical industry, particularly in formulations aimed at treating certain diseases due to their biological activity.
  • Antioxidant Properties: The hydroxyl groups in 4-(4-hydroxyphenyl)sulfonylphenol contribute to its antioxidant capabilities, which can help in reducing oxidative stress, a significant factor in many health issues.
  • Environmental Relevance: Studies have suggested that compounds with similar structures may serve as a basis for developing environmentally friendly materials and processes, addressing concerns related to sustainability.
  • Analytical Chemistry: This compound is often employed as a standard in analytical methods, providing a benchmark for assessing the behavior of sulfonyl compounds in various chemical environments.

As a chemistry student or scientist, understanding compounds like 4-(4-hydroxyphenyl)sulfonylphenol is essential for unraveling the complexities of chemical reactivity and applications in real-world scenarios. "The journey of learning about such compounds not only broadens our knowledge but also challenges us to think critically about their applications in technology, health, and the environment."


Synonyms
4,4'-Sulfonyldiphenol
80-09-1
Bisphenol S
Bis(4-hydroxyphenyl) sulfone
Phenol, 4,4'-sulfonylbis-
4-(4-hydroxyphenyl)sulfonylphenol
4,4'-Dihydroxydiphenyl sulfone
4-Hydroxyphenyl sulfone
4,4'-Sulfonylbisphenol
Bis(p-hydroxyphenyl) sulfone
Diphone C
Bis(4-hydroxyphenyl)sulfone
4,4-Sulfonyldiphenol
Sulphonylbisphenol
4,4'-Bisphenol S
1,1'-Sulfonylbis(4-hydroxybenzene)
Bis(p-hydroxyphenyl)sulfone
BPS 1
4,4'-Sulphonyldiphenol
P,P'-Dihydroxydiphenyl sulfone
NSC 8712
PHENOL, 4,4'-SULFONYLDI-
BISPHENOL-S
CCRIS 2647
NSC 683541
EINECS 201-250-5
DHDPhS
BRN 2052954
3OX4RR782R
DTXSID3022409
CHEBI:34372
AI3-08667
HSDB 8087
NSC-8712
4-[(4-hydroxyphenyl)sulfonyl]phenol
MFCD00002350
NSC-683541
DTXCID602409
4,4'-dihydroxy diphenyl sulfone
NSC8712
4-(4-hydroxyphenylsulfonyl)phenol
EC 201-250-5
4-06-00-05809 (Beilstein Handbook Reference)
EINECS 247-158-9
1,1'-Sulfonylbis[4-hydroxybenzene]
NSC 57909
NSC683541
BIS(4-HYDROXY(PHENYL))SULFONE
BIS(4-HYDROXY(PHENYL))SULPHONE
1, 1'-SULFONYLBIS(4-HYDROXYBENZENE)
25641-61-6
CAS-80-09-1
C12H10O4S
bisphenols
UNII-3OX4RR782R
4,4'-dihydroxydiphenylsulfone
4,4'-Dihydroxydiphenyl sulphone
4-(4-hydroxybenzenesulfonyl)phenol
4,4'Bisphenol S
4,4'Sulfonylbisphenol
4,4'Sulphonyldiphenol
Phenol,4'-sulfonylbis-
4,4\'-sulfonyldiphenol
Phenol, 4,4'sulfonyldi
WLN: QR DSWR DQ
Bis(phydroxyphenyl)sulfone
bis(4hydroxyphenyl)sulfone
Phenol, 4,4'sulfonylbis
Bisphenol S (4,4')
ChemDiv3_000253
Bis(phydroxyphenyl) sulfone
4,4'-Sulfonylbis[phenol]
bis(4hydroxyphenyl) sulfone
Cambridge id 5137133
di-(4-Hydroxyphenyl)sulfone
Oprea1_709121
SCHEMBL18838
p,p'Dihydroxydiphenyl sulfone
MLS001195068
4,4'dihydroxydiphenyl sulfone
BIDD:ER0209
bis(4-hydroxylphenyl) sulfone
4,4'-Dihydroxydiphenylsulphone
4,4'-dihydroxy diphenylsulfone
CHEMBL384441
4,4'-Sulfonyldiphenol, 98%
4,4'-Sulfonyldiphenol (4,4'-Dihydroxydiphenylsulfone)
BP_06 (BPS)
1,1'Sulfonylbis(4hydroxybenzene)
Bisphenol??S, analytical standard
HMS2866C04
Tox21_201743
Tox21_302843
BBL004108
MSK000912
STK267009
AKOS000119535
CS-W012643
DS-5781
FB62571
HY-W011927
IDI1_019571
NCGC00164029-01
NCGC00164029-02
NCGC00256437-01
NCGC00259292-01
AC-11720
SMR000554491
B0495
EU-0066997
NS00010610
EN300-18083
E82999
AB00275288-05
Q418379
Z57158549
F0266-0794
Bisphenol S;4,4'-Dihydroxydiphenyl Sulfone;4,4'-Sulfonyldiphenol
247-158-9
6JD
InChI=1/C12H10O4S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8,13-14