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Chloroxylenol

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Identification
Molecular formula
C9H11ClO
CAS number
88-04-0
IUPAC name
4-chloro-5-isopropyl-2-methyl-phenol
State
State

At room temperature, chloroxylenol is solid. It exists in crystalline form and is stable under normal conditions.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
156.61g/mol
Molar mass
156.6090g/mol
Density
1.3000g/cm3
Appearence

Chloroxylenol typically appears as a colorless to pale yellow crystalline solid. It may sometimes have a faint phenolic odor.

Comment on solubility

Solubility of 4-chloro-5-isopropyl-2-methyl-phenol

The solubility of 4-chloro-5-isopropyl-2-methyl-phenol can be categorized based on several factors related to its chemical structure and environmental interactions. Here are some key points to consider:

  • Polar vs Nonpolar: This compound contains both polar and nonpolar characteristics due to its hydroxyl group (-OH) and aromatic ring structure. This duality influences its solubility in different solvents.
  • Water Solubility: Generally, compounds with hydroxyl groups are expected to be soluble in water. However, the large isopropyl and chloro substituents can hinder full solubility. Therefore, while 4-chloro-5-isopropyl-2-methyl-phenol may show some level of solubility in water, it is likely to be limited.
  • Solvent Compatibility: The compound is more likely to be soluble in organic solvents such as ethanol, acetone, or dichloromethane, which can better encompass the hydrophobic regions of the molecule.
  • Temperature Dependence: Solubility can vary with temperature; increasing the temperature typically enhances the solubility of solid compounds in liquids, thereby potentially aiding the dissolution process of 4-chloro-5-isopropyl-2-methyl-phenol.

In conclusion, the solubility of 4-chloro-5-isopropyl-2-methyl-phenol presents a nuanced picture, largely dictated by its chemical makeup and the environment it exists in. As with many organic compounds, understanding these solubility parameters is critical for applications in various scientific and industrial fields.

Interesting facts

Interesting Facts about 4-Chloro-5-Isopropyl-2-Methyl-Phenol

4-Chloro-5-isopropyl-2-methyl-phenol is a fascinating compound that belongs to the class of phenolic compounds. Here are some intriguing insights into this compound:

  • Chemical Behavior: The presence of the chloro group and isopropyl group in its structure contributes to unique reactivity, making this compound a valuable building block in organic synthesis.
  • Applications: Often utilized in the production of various antiseptics and disinfectants, this compound showcases its effectiveness in combating microbial growth, making it indispensable in pharmaceuticals and personal care products.
  • Phenolic Compounds: As a member of the phenolic family, it shares characteristics with other phenols, which are known for their antioxidant properties. This adds another layer of interest regarding its potential health impacts.
  • Ecological Role: Research into phenolic compounds often highlights their role in plant physiology. This compound could also be studied for its environmental interactions and impact on ecosystems.
  • Safety Considerations: While beneficial, phenolic compounds can pose risks. Understanding the toxicity and safety profile of 4-chloro-5-isopropyl-2-methyl-phenol is crucial for its safe use in various applications.

In summary, 4-chloro-5-isopropyl-2-methyl-phenol is more than just a chemical; it is an important compound that allows scientists to develop innovative solutions in health and environmental science. As with many chemicals, continued research is essential to unveil its full potential and ensure safe handling.

Synonyms
Chlorcarvacrol
5665-94-1
Carvasept
Monochloroisothymol
CARVACROL, 5-CHLORO-
4-CHLORO-5-ISOPROPYL-2-METHYLPHENOL
chlorocarvacrol
EINECS 227-122-9
NSC 26130
BRN 3239606
NSC-26130
5-CHLORO-CARVACROL
5EL163606Q
CHLOROCARVACROL [WHO-DD]
DTXSID40205219
4-06-00-03333 (Beilstein Handbook Reference)
4-CHLORO-2-METHYL-5-ISOPROPYLPHENOL
chlor-carvacrol
DTXCID90127710
5-Chlorocarvacrol
MCIT
4-chloro-2-methyl-5-propan-2-ylphenol
LABOTEST-BB LT00233115
4-chloro-2-methyl-5-(propan-2-yl)phenol
Phenol, 4-chloro-2-methyl-5-(1-methylethyl)-
5-chlorcarvacrol
4-Chloro-2-methyl-5-(1-methylethyl)phenol
UNII-5EL163606Q
Carvacrol derivative, 15
SCHEMBL1443139
TQP1210
BDBM248168
WLN: QR DG B1 EY1&1
LABOTEST-BBLT00233115
FAA66594
NSC26130
4-Chloro-5-isopropyl-2-methyl phenol
AKOS000121021
NS00033559
EN300-21282
10.14272/AFFXNOIULZQAML-UHFFFAOYSA-N.1
doi:10.14272/AFFXNOIULZQAML-UHFFFAOYSA-N.1
Q27261922
Z104495034