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4-Chloro-2-methoxyphenol

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Identification
Molecular formula
C7H7ClO2
CAS number
95-88-5
IUPAC name
4-chloro-2-methoxy-phenol
State
State

At room temperature, 4-Chloro-2-methoxyphenol is a solid compound.

Melting point (Celsius)
54.00
Melting point (Kelvin)
327.15
Boiling point (Celsius)
265.40
Boiling point (Kelvin)
538.50
General information
Molecular weight
158.58g/mol
Molar mass
158.5780g/mol
Density
1.3616g/cm3
Appearence

4-Chloro-2-methoxyphenol appears as a white crystalline solid. It is known for its distinct and characteristic chemical odor.

Comment on solubility

Solubility of 4-chloro-2-methoxy-phenol

4-chloro-2-methoxy-phenol, also known as p-chloro-methoxyphenol, exhibits intriguing solubility characteristics that are crucial for its applications in various fields. The solubility of this compound can be summarized as follows:

Key Solubility Factors

  • Polarity: The presence of both a chloro group and a methoxy group contributes to the polarity of the molecule, affecting its interaction with solvents.
  • Solvents: 4-chloro-2-methoxy-phenol is generally more soluble in organic solvents such as ethanol and acetone, and less soluble in water due to its hydrophobic characteristics.
  • Temperature: Solubility can increase with temperature, as is common with many organic compounds.

In summary, while 4-chloro-2-methoxy-phenol is not highly soluble in water, its solubility in organic solvents makes it versatile for various chemical applications. This compound serves as a potent ingredient in formulations where oil or organic solvent bases are utilized.

Interesting facts

Interesting Facts about 4-Chloro-2-methoxy-phenol

4-Chloro-2-methoxy-phenol, commonly known as Chlorothymol, is a fascinating compound with a variety of applications in both industry and research. Here are some compelling facts about this chemical:

  • Antimicrobial Properties: Chlorothymol is well-regarded for its antimicrobial activity, making it a valued component in various antiseptic and disinfectant formulations. Its efficacy against a broad spectrum of microorganisms supports its use in hygiene products.
  • Natural Occurrence: This compound is derived from thymol, which is naturally found in thyme oil. The ability to provide similar properties while being slightly modified for better effectiveness is a fascinating aspect of its chemistry.
  • Applications in Medicine: In addition to its antiseptic uses, Chlorothymol has been evaluated for medicinal applications, including potential roles in oral healthcare products due to its pleasant scent and effectiveness in combating oral bacteria.
  • Flavor and Fragrance Industry: The compound's characteristic aromatic profile makes it a favored ingredient in flavoring and fragrance formulations, contributing to the sensory experiences in food and personal care products.
  • Research Potential: Ongoing studies explore its varied pharmacological properties, particularly its antioxidant effects and implications in broader medical treatments. The research community continues to uncover its potential benefits.

As a reminder of the compound's complexity, *"In science, we see the elegance of simplicity; yet, in our molecules, we often find issues of remarkable complexity."* Understanding the behavior and benefits of compounds like 4-chloro-2-methoxy-phenol is crucial in advancing both scientific knowledge and practical applications.


Synonyms
4-CHLOROGUAIACOL
4-Chloro-2-methoxyphenol
16766-30-6
Phenol, 4-chloro-2-methoxy-
MFCD00070774
2-Methoxy-4-chloro-phenol
CHEMBL3416134
4-chloro-2-methoxy-phenol
4-Chloro-2-methoxyphenol #
Phenol,4-chloro-2-methoxy-
SCHEMBL363972
orb1693597
SCHEMBL1639475
SCHEMBL1805452
SCHEMBL7959656
DTXSID0074974
FVZQMMMRFNURSH-UHFFFAOYSA-
BDBM50498196
AKOS005207163
FC70097
HY-W039169
PS-5170
PD158369
SY048539
4-Chloro-2-methoxyphenol, technical grade
DB-012929
CS-0096842
ST50824721
EN300-192546
F20981
InChI=1/C7H7ClO2/c1-10-7-4-5(8)2-3-6(7)9/h2-4,9H,1H3