Bisphenol S | Solubility of Things

Identification

Molecular formula

C₁₂H₁₀O₃S

CAS number

80-09-1

IUPAC name

4-(4-hydroxyphenyl)sulfanylphenol

State

Bisphenol S is typically in a solid state at room temperature. The compound's high melting point indicates it remains solid under normal environmental conditions.

Melting point (Celsius)

245.00

Melting point (Kelvin)

518.15

Boiling point (Celsius)

581.00

Boiling point (Kelvin)

854.15

General information

Molecular weight

250.32g/mol

Molar mass

250.3180g/mol

Density

1.3700g/cm³

Appearence

Bisphenol S appears as a white crystalline solid or powder. It is typically odorless and stable under normal conditions. Its appearance can vary slightly based on its purity and the specific form it is in.

Comment on solubility

Solubility of 4-(4-hydroxyphenyl)sulfanylphenol

The solubility of 4-(4-hydroxyphenyl)sulfanylphenol, also known as thiodiphenol, can be impacted by several factors, including the presence of functional groups and the compound's molecular structure. Here are some key points to consider:

Polar vs Non-Polar Solvents: Generally, this compound is expected to exhibit higher solubility in polar solvents due to the presence of hydroxyl (–OH) groups that can engage in hydrogen bonding.
Influence of Hydroxyl Groups: With both phenolic groups containing hydroxyl groups, the molecule potentially enhances interaction with water, although steric hindrance may also play a role in limiting solubility.
pH Effects: The solubility can vary significantly with pH. In acidic conditions, protonation of the hydroxyl groups may occur, affecting solubility characteristics.
Temperature Dependence: As with many organic compounds, increased temperature can lead to increased solubility, suggesting that thermal conditions should be considered when working with this compound.

In conclusion, while 4-(4-hydroxyphenyl)sulfanylphenol shows promise for solubility in polar solvents, understanding its behavior under different conditions is essential for optimal application. Therefore, assessing its solubility in practical scenarios is vital for effective usage in various fields.

Interesting facts

Interesting Facts about 4-(4-hydroxyphenyl)sulfanylphenol

4-(4-hydroxyphenyl)sulfanylphenol, often referred to in the scientific community for its intriguing properties, belongs to a class of compounds known as phenolic sulfides. This compound showcases a unique combination of functional groups that gives it interesting applications and potential in various fields.

Key Characteristics

Antioxidant Properties: Its phenolic structure suggests strong antioxidant capabilities, which makes it a potential candidate for use in protective formulations.
Biological Relevance: This compound may play a role in medicinal chemistry, as many sulfanyl phenols are investigated for their biological activities, including antimicrobial and anticancer properties.
Environmental Considerations: Due to its structure, the compound can act as a building block for designing eco-friendly materials, contributing to sustainable chemistry practices.

Applications and Uses

Research on 4-(4-hydroxyphenyl)sulfanylphenol delves into its multi-faceted applications:

Utilized in the development of antioxidant additives for plastics and food preservation.
Explored as a therapeutic agent in pharmaceutical formulations due to its promising biological activities.
Acts as a precursor in the synthesis of various organic compounds, enhancing its value in synthetic chemistry.

Research Insights

Ongoing studies highlight the significance of the bonding pattern in this compound:

The positioning of the hydroxyl and sulfanyl groups can influence its reactivity and interaction with biological systems.
Comparative analysis with similar phenolic compounds reveals how subtle changes in structure can dramatically affect performance and function.

In conclusion, 4-(4-hydroxyphenyl)sulfanylphenol represents a fascinating intersection of chemistry and biology, inviting further research to unlock its potential in both industrial and therapeutic applications. Its complex structure and diverse properties make it a compelling subject for chemists and researchers alike.

Synonyms

4,4'-Thiodiphenol

2664-63-3

Phenol, 4,4'-thiobis-

Bis(4-hydroxyphenyl) sulfide

4,4'-Thiobisphenol

4,4'-Dihydroxydiphenyl sulfide

Thiobisphenol

p,p'-Dihydroxydiphenyl sulfide

Bis(4-oxyphenyl)sulfide

4,4'-Dioxydiphenyl sulfide

PHENOL, 4,4'-THIODI-

Bis(p-hydroxhphenyl) sulfide

Sulfide, bis(4-hydroxyphenyl)

4,4'-Dihydroxydiphenylsulfide

4,4'-sulfanediyldiphenol

4,4'-Dioxydiphenylsulfide

4-(4-hydroxyphenylthio)phenol

NSC 203030

CHEBI:38957

EINECS 220-197-9

NGN288M6MM

4,4`-Thiodiphenol

DTXSID9047960

NSC-203030

PHENOL, P,P'-THIODI-

PHENOL, P,P'-THIOBIS-

DTXCID5027936

TDP cpd

4,4'Thiobisphenol

Bis(4oxyphenyl)sulfide

Phenol, 4,4'thiodi

Phenol, 4,4'thiobis

4,4'Dioxydiphenylsulfide

4,4'Dioxydiphenyl sulfide

Bis(phydroxhphenyl) sulfide

Bis(4hydroxyphenyl) sulfide

4,4'dihydroxydiphenylsulfide

p,p'Dihydroxydiphenyl sulfide

Sulfide, bis(4hydroxyphenyl)

4,4'dihydroxydiphenyl sulfide

220-197-9

4,4'-thiobis-phenol

4-(4-hydroxyphenyl)sulfanylphenol

4-[(4-hydroxyphenyl)sulfanyl]phenol

4,4-Thiodiphenol

4,4-Thiobis-phenol

4,4'-Dihydroxy diphenyl sulfide

CHEMBL3183502

UNII-NGN288M6MM

4,4-Dihydroxydiphenyl sulfide

A8K

MFCD00002349

Phenol,4'-thiodi-

Phenol,4'-thiobis-

4,4\'-thiodiphenol

4,4'-Thio-diphenol

4.4/'-Thiodiphenol

4-Hydroxyphenyl sulfide

4,4'-Thiobis[phenol]

4,4-Dihydroxydiphenylsulfide

Oprea1_271899

SCHEMBL29726

4,4'-Thiodiphenol, 99%

4-Hydroxyphenyl sulfide; TDP

BIDD:ER0084

VWGKEVWFBOUAND-UHFFFAOYSA-

STR04624

Tox21_200973

BDBM50515033

NSC203030

STK672128

AKOS000120152

CS-W014789

FD32799

NCGC00248889-01

NCGC00248889-02

NCGC00258526-01

AC-16455

CAS-2664-63-3

DB-022669

D1356

NS00014378

EN300-20642

E83012

AB01333629-02

SR-01000596915

SR-01000596915-1

Q27118057

F0902-7612

Z104479422

InChI=1/C12H10O2S/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8,13-14H