Interesting facts
Interesting Facts About 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol
2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol is a fascinating compound with various applications in chemistry and industry. This compound is a derivative of benzene, which is known for its unique properties and versatility. Here are some intriguing aspects:
- Structural Complexity: The structure of 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol features a benzene ring substituted with two bulky alkyl groups, specifically two 1,1-dimethylpropyl groups. This complexity gives it unique physical and chemical properties.
- Potential Applications: Compounds like this one are often researched for use in the production of antioxidants, which play a critical role in preventing oxidative damage in various materials and biological systems.
- Environmental Impact: The study of such compounds also extends to their potential environmental impact. Investigating the biodegradability and toxicity of such molecules is essential in the field of environmental chemistry.
- Research Interest: Due to its unique structure, 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol has caught the attention of researchers exploring novel materials for drugs, polymers, and other functional chemicals.
- Polar vs. Nonpolar: The presence of both hydrophobic (the alkyl side chains) and hydrophilic (the diol) parts in its structure results in interesting solubility characteristics, making it an important study in understanding molecular interactions.
In summary, 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol is more than just a chemical compound; its unique structure leads to various applications and interests in the fields of chemistry, materials science, and sustainability. As scientists continue to explore its functionality, we can expect to uncover even more about its potential.
Synonyms
79-74-3
2,5-Di-tert-amylhydroquinone
2,5-Di-tert-pentylbenzene-1,4-diol
2,5-Di-tert-pentylhydroquinone
Santouar A
Santovar A
Diamylhydroquinone
2,5-bis(2-methylbutan-2-yl)benzene-1,4-diol
Antage DAH
Dahq
USAF B-21
1,4-Benzenediol, 2,5-bis(1,1-dimethylpropyl)-
2,5-DI(TERT-AMYL)HYDROQUINONE
2,5-Di-t-amylhydroquinone
Hydroquinone, 2,5-di-tert-pentyl-
2,5-DI-T-PENTYLHYDROQUINONE
Hydroquinone, 2,5-di-t-pentyl-
NSC 455
Hydroquinone, 2,5-di-tert-amyl-
2,5-Bis(1,1-dimethylpropyl)hydroquinone
2,5-Di-tert-amylbenzene-1,4-diol
2,5-Bis(1,1-dimethylpropyl)-1,4-benzenediol
HSDB 5231
EINECS 201-222-2
BRN 2214556
19O4J76TTK
AI3-61041
NSC-455
DTXSID5044992
EC 201-222-2
3-06-00-04748 (Beilstein Handbook Reference)
DI-TERT-PENTYLHYDROQUINONE, 2,5-
2,5-DI-T-PENTYLHYDROQUINONE [HSDB]
2,5-DI-TERT-PENTYLHYDROQUINONE [MI]
Hydroquinone,5-di-tert-amyl-
2,1-dimethylpropyl)hydroquinone
Hydroquinone,5-di-tert-pentyl-
1, 2,5-bis(1,1-dimethylpropyl)-
2,1-dimethylpropyl)-1,4-benzenediol
WLN: 2X1&1&R BQ EQ DX2&1&1
UNII-19O4J76TTK
Lowinox AH25
MFCD00027029
2,5Ditamylhydroquinone
2,5Ditertamylhydroquinone
2,5Ditertpentylhydroquinone
hydroquinone derivative, 5a
Hydroquinone, 2,5ditpentyl
Hydroquinone, 2,5ditertamyl
Oprea1_395030
SCHEMBL34690
2,5Ditertamylbenzene1,4diol
Hydroquinone, 2,5ditertpentyl
2,5Ditertpentylbenzene1,4diol
2,5-Di-t-amyl-p-hydroquinone
2,5-di-tert-amyl-hydroquinone
CHEMBL594135
NSC455
2,5-Di-tert.-pentylhydrochinon
DTXCID3024992
BDBM34117
NSC6267
NSC-6267
Tox21_301767
BBL002922
STK378237
AKOS005448322
2,5Bis(1,1dimethylpropyl)hydroquinone
2,5-Ditert-pentyl-1,4-benzenediol #
CAS-79-74-3
NCGC00256161-01
NCGC00340536-01
VS-01261
2,5Bis(1,1dimethylpropyl)1,4benzenediol
1,4Benzenediol, 2,5bis(1,1dimethylpropyl)
CS-0319422
D0299
NS00008202
AB01333681-02
Q27252125
201-222-2
Solubility of 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol
The compound 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol, also known as a highly substituted phenolic compound, exhibits unique solubility characteristics that depend on various factors. Below are some key points regarding its solubility:
In summary, while 2,5-bis(1,1-dimethylpropyl)benzene-1,4-diol is expected to have limited solubility in water, it is more amenable to dissolution in nonpolar solvents, highlighting the importance of understanding solubility parameters in chemical applications.