Skip to main content

m-Cresol

ADVERTISEMENT
Identification
Molecular formula
C9H12O
CAS number
618-45-1
IUPAC name
3-isopropylphenol
State
State

At room temperature, 3-isopropylphenol is typically a liquid. Its state can vary depending on environmental conditions, and it may crystallize at lower temperatures.

Melting point (Celsius)
9.00
Melting point (Kelvin)
282.15
Boiling point (Celsius)
219.00
Boiling point (Kelvin)
492.15
General information
Molecular weight
136.19g/mol
Molar mass
136.1930g/mol
Density
0.9697g/cm3
Appearence

3-Isopropylphenol appears as a colorless to pale yellow liquid. It can solidify when cooled, forming crystals. In its liquid state, it has an aromatic odor resembling that of phenol, albeit sweeter.

Comment on solubility

Solubility of 3-isopropylphenol

3-isopropylphenol, a compound with the chemical formula C10H14O, exhibits interesting solubility characteristics that are influenced by its molecular structure.

Generally, the solubility of 3-isopropylphenol can be summarized as follows:

  • In **water**, 3-isopropylphenol has limited solubility due to its relatively hydrophobic isopropyl group, which does not favorably interact with water molecules.
  • In **organic solvents** such as ethanol, methanol, and diethyl ether, it demonstrates a much higher solubility because these solvents have similar non-polar characteristics that can interact with the compound's aromatic ring.
  • Its solubility may also be influenced by temperature; typically, like many organic compounds, its solubility might increase with higher temperatures.

In summary, while *3-isopropylphenol* does not dissolve well in water, it is fairly soluble in a variety of organic solvents. This solubility profile is crucial for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 3-Isopropylphenol

3-Isopropylphenol, also known as 3-(1-methylethyl)phenol, is a fascinating aromatic compound with diverse applications and properties. Here are some intriguing insights:

  • Natural Occurrence: This compound is found in various essential oils, contributing to the characteristic scent and flavor profiles of certain plants.
  • Biological Activity: Research suggests that 3-isopropylphenol exhibits antimicrobial properties, making it a potential candidate for use in antiseptics and preservatives.
  • Industrial Uses: Commonly utilized in the production of resins and plastics, 3-isopropylphenol serves as a crucial intermediate in the synthesis of various chemical products.
  • Phenolic Compound: As a phenol derivative, it shares the traits typical to phenolic substances, such as antioxidant activity, and can play a role in protecting against oxidative stress.
  • Research Potential: Continuous studies explore its role in pharmaceuticals and agriculture, indicating that this compound may harbor more undiscovered applications.

In summary, 3-isopropylphenol is not just another compound; it embodies the intersection of nature and science, revealing the potential that can arise from studying aromatic constituents.

Synonyms
3-Isopropylphenol
618-45-1
M-ISOPROPYLPHENOL
m-Cumenol
3-propan-2-ylphenol
Phenol, m-isopropyl-
Phenol, 3-(1-methylethyl)-
3-(1-Methylethyl)phenol
3-(propan-2-yl)phenol
ISOPROPYLPHENOL, META
3-isopropyl-phenol
MFCD00002301
ERD00478GH
DTXSID0044571
NSC-2209
3-Isopropylhydroxybenzene
NSC 2209
3-isopropyl phenol
EINECS 210-551-0
BRN 2040880
UNII-ERD00478GH
AI3-18885
3-(1-Methylethyl)phenol; Propofol Imp. F (EP); Propofol Impurity F
m-Isopropyl phenol
m-Isopropyl-phenol
meta-isopropylphenol
EINECS 291-826-2
phenol, 3-isopropyl-
Carvacrol derivative, 10
3-Isopropylphenol, 97%
EC 291-826-2
ISOPROPYLPHENOL, M-
SCHEMBL51528
4-06-00-03214 (Beilstein Handbook Reference)
CHEMBL449684
DTXCID8024571
NSC2209
BDBM248167
Tox21_301558
AKOS000121413
NCGC00255721-01
AS-10581
CAS-618-45-1
PROPOFOL IMPURITY F [EP IMPURITY]
NS00002341
EN300-21143
D87686
Q27277323
Z104492878