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2,3,5-trimethylhydroquinone

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Identification
Molecular formula
C9H12O2
CAS number
700-13-0
IUPAC name
2,3,5-trimethylbenzene-1,4-diol
State
State

At room temperature, 2,3,5-trimethylhydroquinone is typically found in a solid state.

Melting point (Celsius)
126.00
Melting point (Kelvin)
399.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
166.22g/mol
Molar mass
166.2190g/mol
Density
1.1210g/cm3
Appearence

2,3,5-Trimethylhydroquinone typically appears as a solid crystalline substance. The crystals are often white or off-white, sometimes appearing as colorless solids depending on their purity.

Comment on solubility

Solubility of 2,3,5-trimethylbenzene-1,4-diol

2,3,5-trimethylbenzene-1,4-diol, a diol compound, displays interesting solubility characteristics that can be summarized as follows:

  • Polar Nature: The presence of hydroxyl (–OH) groups in the molecule contributes to its polar nature, which generally aids in solubility in polar solvents.
  • Hydrogen Bonding: The –OH groups are capable of forming hydrogen bonds with water molecules, enhancing its solubility in aqueous solutions.
  • Solvent Compatibility: While 2,3,5-trimethylbenzene-1,4-diol is soluble in water, it may also exhibit solubility in various organic solvents, depending on their polarity.
  • Temperature Dependence: Like many compounds, its solubility may increase with temperature, making it favorable for dissolving in hot solvents.

Overall, the solubility of 2,3,5-trimethylbenzene-1,4-diol can be described as good in polar solvents, particularly water, due to its ability to engage in hydrogen bonding and its polar functional groups.

Interesting facts

Interesting Facts about 2,3,5-Trimethylbenzene-1,4-diol

2,3,5-Trimethylbenzene-1,4-diol, also known as a polyhydroxylated aromatic compound, has quite a fascinating role in various fields of chemistry and industry. Here are some engaging facts about this compound:

  • Chemical Structure and Functionality: This compound consists of a benzene ring substituted with three methyl groups and two hydroxyl groups, making it a key player in organic synthesis and industrial applications.
  • Applications: It is often utilized in the manufacture of resins and polymers, as its unique structure provides excellent properties for these materials.
  • Environmental Impact: Its derivatives can function as antioxidants or additives in various products, helping to improve longevity and stability while also reducing environmental footprint.
  • Biological Activities: Some studies suggest that compounds similar to 2,3,5-trimethylbenzene-1,4-diol exhibit notable biological activities, including potential antioxidant effects, which can be beneficial for human health.
  • Flavor and Fragrance: The presence of such compounds is sometimes linked to the creation of specific flavor and fragrance compounds, contributing to the aromatic profiles in various products.

Overall, 2,3,5-trimethylbenzene-1,4-diol serves as an excellent example of how intricate chemistry can lead to substantial impacts in daily life, from improving industrial processes to enhancing consumer products. As researchers continuously explore its properties and potential, there is no telling what other applications this compound might find!

Synonyms
Trimethylhydroquinone
700-13-0
2,3,5-Trimethylhydroquinone
Pseudocumohydroquinone
1,4-Benzenediol, 2,3,5-trimethyl-
psi-Cumohydroquinone
2,3,6-Trimethylhydroquinone
2,3,5-Trimethylquinol
.psi.-Cumohydroquinone
2,3,5-Trimethyl-1,4-benzenediol
HYDROQUINONE, TRIMETHYL-
NSC 401617
EINECS 211-838-3
GSY6340N4A
DTXSID7052446
AI3-61040
NSC-401617
DTXCID9031018
CHEBI:176794
EC 211-838-3
psiCumohydroquinone
trimethylhydrochinon
Trimethylphydroquinone
Hydroquinone, trimethyl
2,3,5Trimethylquinol
3,6Dihydroxypseudocumol
3,6Dihydroxypseudocumene
2,3,6Trimethylhydroquinone
2,3,5Trimethyl1,4benzenediol
2,3,5Trimethylbenzene1,4diol
1,4Benzenediol, 2,3,5trimethyl
1,4Dihydroxy2,3,5trimethylbenzene
211-838-3
2,3,5-trimethylbenzene-1,4-diol
2,3,5-Trimethyl-benzene-1,4-diol
Trimethyl hydroquinone
MFCD00002346
1,4-Dihydroxy-2,3,5-trimethylbenzene
Trimethylhydroquinone, 97%
UNII-GSY6340N4A
trimethyihydroquinone
TMHYDROP
trimethyl-hydroquinone
2,5-Trimethylhydroquinone
2,6-Trimethylhydroquinone
1, 2,3,5-trimethyl-
A1D7Z
2,5,6-trimethylhydroquinone
SCHEMBL70458
2,3,5-trimethyl hydroquinone
CHEMBL3182864
2,5-Trimethyl-1,4-benzenediol
Tox21_113944
NSC401617
STK062643
AKOS000493632
CS-W018094
FT40555
HY-W017378
NCGC00262952-01
NCGC00262952-02
AC-17918
AS-12795
CAS-700-13-0
NS00009435
T0477
EN300-67505
F71219
AB00694314-03
SR-01000944714
SR-01000944714-1
Q27279264
F3145-3277
InChI=1/C9H12O2/c1-5-4-8(10)6(2)7(3)9(5)11/h4,10-11H,1-3H