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2,4-Dihydroxybenzophenone

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Identification
Molecular formula
C13H10O3
CAS number
131-56-6
IUPAC name
bis(2,4-dihydroxyphenyl)methanone
State
State

At room temperature, 2,4-Dihydroxybenzophenone is typically found in a solid state. It is a stable compound under normal storage conditions and is not volatile.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
352.70
Boiling point (Kelvin)
625.85
General information
Molecular weight
214.22g/mol
Molar mass
214.2090g/mol
Density
1.3532g/cm3
Appearence

2,4-Dihydroxybenzophenone appears as an off-white to light yellow crystalline powder. It exhibits a very faint aromatic odour. The compound is known for its stability under normal conditions, although it may change appearance on prolonged exposure to air and light, which can lead to slight darkening.

Comment on solubility

Solubility of bis(2,4-dihydroxyphenyl)methanone

bis(2,4-dihydroxyphenyl)methanone, also known as bisphenol M, exhibits interesting solubility characteristics that are pivotal in various applications. The solubility of this compound can be influenced by several factors:

  • Polar solvents: Due to the presence of multiple hydroxyl (-OH) groups, bis(2,4-dihydroxyphenyl)methanone is generally soluble in polar solvents like water and alcohols. The hydrogen bonding interactions enhance the solubility in these media.
  • Non-polar solvents: Conversely, its solubility in non-polar solvents is significantly lower, reflecting its structural characteristics that favor interactions with polar environments.
  • pH dependence: The solubility can also be pH-dependent; alterations in pH can affect the ionization of the hydroxyl groups, thereby influencing the overall solubility in aqueous solutions.
  • Temperature effects: Increasing temperature typically enhances solubility, which is particularly relevant in practical applications, such as synthesis processes and pharmaceuticals.

In summary, “the solubility of bis(2,4-dihydroxyphenyl)methanone is a complex interplay of molecular interactions” that make it versatile for various solvation scenarios. Whether in polar or solvent systems, understanding this solubility profile is essential for its effective application in scientific and industrial contexts.

Interesting facts

Interesting Facts about bis(2,4-dihydroxyphenyl)methanone

bis(2,4-dihydroxyphenyl)methanone, commonly referred to by its other names such as Bisphenol A derivative, is a fascinating compound that serves as an essential building block in various chemical applications.

Key Features

  • Dual Hydroxy Groups: This compound contains two hydroxyl (-OH) groups that are connected to phenyl rings, making it a noteworthy example of a phenolic compound.
  • Applications in Industry: It is primarily used in the synthesis of polymers, particularly polycarbonates and epoxy resins, which contribute enormously to modern materials science.
  • Biological Interest: Due to its structural similarities to hormonal structures, it has garnered attention as a compound of interest in studies on endocrine disruptors.
  • Environmental Impact: Researchers are actively studying bis(2,4-dihydroxyphenyl)methanone for its potential effects on aquatic life, making it a compound of concern in environmental chemistry.

Chemical Behavior

This compound's unique molecular structure allows it to participate in various chemical reactions such as esterification and condensation, leading to the creation of complex molecules. Its reactivity is crucial in developing new materials that enhance durability and performance.

Fun Fact

Interestingly, the name bis(2,4-dihydroxyphenyl)methanone reflects its chemical structure, where “bis” signifies the presence of two identical groups, indicating the compound's symmetry and balanced nature.

In summary, bis(2,4-dihydroxyphenyl)methanone is not just a chemical formula; it embodies a wide range of industrial applications and research implications, embodying the intersection of chemistry, biology, and environmental science.

Synonyms
2,2',4,4'-Tetrahydroxybenzophenone
131-55-5
Bis(2,4-dihydroxyphenyl)methanone
Benzophenone-2
Methanone, bis(2,4-dihydroxyphenyl)-
Uvinol D-50
Uvinul D-50
benzophenone 2
2,2',4,4'-Tetrehydroxybenzophenone
2,4,2',4'-Tetrahydroxybenzophenone
NSC 38556
2,2',4,4'-hydroxybenophenone
BENZOPHENONE, 2,2',4,4'-TETRAHYDROXY-
PRR8K3H9VN
EINECS 205-028-9
MFCD00002278
2,2',4,4'-Tetrahydroxy-benzophenone
BRN 1914746
DTXSID5041306
NSC-38556
DTXCID3021306
HSDB 8386
2,2?,4,4?-Tetrahydroxybenzophenone
CAS-131-55-5
UNII-PRR8K3H9VN
di2,4-dihydroxyphenyl ketone
4mgc
27M
ST055642
UVINUL D50
Oprea1_250768
SCHEMBL39507
2,4'-Tetrahydroxybenzophenone
BIDD:ER0038
Methanone,4-dihydroxyphenyl)-
BENZOPHENONE-2 [INCI]
CHEMBL3185091
2,4,4'-Tetrahydroxybenzophenone
Di(2,4-dihydroxyphenyl)methanone
2,2',4,4'-Hydroxybenozphenone
2,2',4'-Tetrahydroxybenzophenone
BDBM234390
BP_28
BCP25884
NSC38556
Tox21_202288
Tox21_303639
BBL012188
STK803083
2,2',6,6'-tetrahydroxybenzophenone
Benzophenone,2',4,4'-tetrahydroxy-
2, 2',4,4'-tetrahydroxybenzophenone
2,2',4,4'-tetrahydroxy benzophenone
AKOS002319293
FT55663
2,2\',4,4\'-Tetrahydroxybenzophenone
NCGC00249205-01
NCGC00249205-02
NCGC00257395-01
NCGC00259837-01
2,2',4,4'-Tetrahydroxy diphenyl ketone
AC-10378
AS-13615
SY020047
DB-042043
2,2',4,4'-Tetrahydroxybenzophenone, 97%
CS-0089098
NS00002972
T0118
H10707
SR-01000199334
SR-01000199334-1
Q27286728
2,2 inverted exclamation mark ,4,4 inverted exclamation mark -Tetrahydroxybenzophenone
205-028-9