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Chlorohydroquinone

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Identification
Molecular formula
C6H4Cl2O2
CAS number
615-46-3
IUPAC name
2,5-dichlorobenzene-1,4-diol
State
State

At room temperature, chlorohydroquinone is in a solid state. It is markedly stable under standard conditions but should be stored in a cool, dry place to preserve its integrity and prevent decomposition, especially avoiding light and moisture exposure which can cause chemical changes in its structure.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
161.00g/mol
Molar mass
161.0020g/mol
Density
1.5800g/cm3
Appearence

Appearance: Chlorohydroquinone is typically a white or off-white crystalline solid. It may occasionally appear as a powder or in crystalline chunks, depending on the lot and the degree of purification. Its clean, white appearance indicates its high purity, especially when freshly produced or well-preserved, while discoloration might suggest impurity or degradation due to exposure to light or oxidizing agents.

Comment on solubility

Solubility of 2,5-dichlorobenzene-1,4-diol

2,5-Dichlorobenzene-1,4-diol (C6H4Cl2O2), a dihydroxy-substituted aromatic compound, exhibits interesting solubility characteristics:

  • Solvent Compatibility: This compound is expected to be sparingly soluble in water due to the presence of hydrophobic chlorinated aromatic rings which hinder extensive interactions with water molecules.
  • Organic Solvents: It demonstrates good solubility in organic solvents such as ethanol, acetone, and dichloromethane, making it favorable for applications in organic chemistry.
  • Temperature Effects: As with many organic compounds, increased temperature generally enhances solubility in organic solvents, promoting better dissolution.
  • Hydrogen Bonding: The hydroxyl (-OH) groups can form hydrogen bonds, which can improve solubility in polar organic solvents but still limit solubility in water.

In conclusion, the solubility of 2,5-dichlorobenzene-1,4-diol is a reflection of its unique chemical structure, balancing both hydrophilic and hydrophobic characteristics. Understanding its solubility is crucial for various applications in chemical synthesis and formulations.

Interesting facts

Interesting Facts about 2,5-Dichlorobenzene-1,4-diol

2,5-Dichlorobenzene-1,4-diol, a fascinating chemical compound, has significant implications both in industrial applications and research. This compound can be recognized by its dual *chlorine* substitutions on the benzene ring, which contribute to its unique properties.

Key Characteristics

  • Structure: The structure consists of a benzene ring with two chlorine atoms and two hydroxyl groups attached, leading to interesting reactivity and potential uses in various applications.
  • Versatility: This compound can serve as an intermediate in the synthesis of other chemicals, further demonstrating its importance in organic chemistry.
  • Biological Relevance: Due to its chemical structure, 2,5-dichlorobenzene-1,4-diol may interact with biological systems, raising questions about its impact on environmental and human health.

Applications

  • Analytical Chemistry: The compound is often used as a standard in chemical analysis to detect other **chlorinated compounds**.
  • Pesticide Production: Due to its chlorinated nature, it may find applications in the development of certain pesticides.
  • Pharmaceutical Development: Its derivatives may play roles in the formation of biologically active compounds, expanding its utility in drug discovery.

As a scientist or chemistry student studying 2,5-dichlorobenzene-1,4-diol, one would appreciate its strategic importance in synthetic chemistry. The ability to manipulate its dual functional groups can lead to innovations in both **material science** and **medicinal chemistry**, showcasing how a seemingly simple compound can have such profound implications.

In summary, 2,5-dichlorobenzene-1,4-diol is more than just a compound; it is a gateway to understanding the complexities of chemical interactions and the diverse applications of chlorinated aromatic compounds in modern chemistry.

Synonyms
2,5-dichlorohydroquinone
824-69-1
2,5-dichlorobenzene-1,4-diol
1,4-Benzenediol, 2,5-dichloro-
2,5-Dichloro-p-hydroquinone
Hydroquinone, 2,5-dichloro-
2,5-Dichloro-1,4-hydroquinone
2,5-Dichloro-p-benzohydroquinone
2,5-DCHQ
2,5-Dichloro-1,4-benzenediol
2,5-Dichloro-1,4-dihydroxybenzene
CCRIS 5677
EINECS 212-533-8
D489X4TQVD
MFCD00041749
NSC 48667
2,5-dichlorohydroquinol
2,5-dichloro-p-quinol
NSC-48667
DTXSID4061179
CHEBI:27545
1,4-dihydroxy-2,5-dichlorobenzene
UNII-D489X4TQVD
2,4-hydroquinone
2,4-dihydroxybenzene
2.5-Dichlorohydroquinone
Hydroquinone,5-dichloro-
bmse000661
SCHEMBL48305
DTXCID7048297
2,5-Dichlorohydroquinone, 98%
2,5-DCH
NSC48667
Hydroquinone, 2,5-dichloro-(8CI)
STL301456
AKOS015889031
AS-77070
CS-0364968
NS00038204
C06600
Q27103188
212-533-8