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4-Methylcyclohexanol

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Identification
Molecular formula
C7H14O
CAS number
589-91-3
IUPAC name
4-methylcyclohexanol
State
State

At room temperature, 4-Methylcyclohexanol is generally a liquid. Its viscous nature is typical of higher chain alcohols and cyclohexanol derivatives.

Melting point (Celsius)
25.00
Melting point (Kelvin)
298.15
Boiling point (Celsius)
181.30
Boiling point (Kelvin)
454.45
General information
Molecular weight
114.19g/mol
Molar mass
114.1850g/mol
Density
0.9304g/cm3
Appearence

4-Methylcyclohexanol is typically a colorless, viscous liquid at room temperature. It can emit a mild, oily odor that is characteristic of alcohols. Its appearance makes it identifiable as a typical cyclohexanol derivative.

Comment on solubility

Solubility of 4-Methylcyclohexanol

4-Methylcyclohexanol, with the chemical formula C7H14O, is a fascinating organic compound with notable solubility characteristics. This compound, like many alcohols, exhibits varying solubility behaviors based on a few key factors:

  • Polarity: The presence of the hydroxyl group (-OH) in 4-methylcyclohexanol imparts a degree of polarity to the molecule, enabling it to engage in hydrogen bonding with water molecules.
  • Hydrophobic and Hydrophilic Balance: While the alkyl groups are hydrophobic, the hydroxyl group is hydrophilic, which creates a balance that influences solubility in various solvents.
  • Temperature Effects: Solubility can increase with higher temperatures, as increased kinetic energy facilitates molecular interactions.

Typically, 4-methylcyclohexanol is soluble in organic solvents such as ethanol, methanol, and acetone, but may have limited solubility in water due to the bulkiness of the cyclohexane ring. Thus, its solubility can be characterized as:

  • Soluble: In organic solvents.
  • Insoluble or Poorly Soluble: In water.

In conclusion, the solubility of 4-methylcyclohexanol demonstrates the intricate balance between molecular structure and solvent interactions. Understanding these solubility properties is essential for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 4-methylcyclohexanol

4-methylcyclohexanol is a fascinating compound with several unique characteristics that make it noteworthy in the world of chemistry. Here are some intriguing points about this saturated alcohol:

  • Structure and Isomerism: As a derivative of cyclohexanol, 4-methylcyclohexanol features a methyl group attached to the cyclohexane ring. This structural arrangement gives rise to various stereoisomers, which can exhibit distinct physical and chemical properties.
  • Industrial Applications: This compound is utilized in the production of surfactants and solvents. Its versatility allows it to play a vital role in various industrial processes, enhancing product formulations in cleaning and coating materials.
  • Odor Characteristics: 4-methylcyclohexanol is known for its pleasant, mild odor. It finds applications in the fragrance industry, where it is incorporated into perfumes and scented products, providing a fresh and subtle aromatic note.
  • Research Significance: In the realm of organic chemistry, 4-methylcyclohexanol serves as an important building block for synthesizing more complex compounds. Researchers often use it in studies related to reaction mechanisms and the development of new materials.
  • Hydrogen Bonding: The hydroxyl (-OH) group in 4-methylcyclohexanol can participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. This property is critical for understanding its behavior in various chemical environments.

In summary, 4-methylcyclohexanol is more than just a simple alcohol. From its intriguing molecular structure to its varied applications, it encompasses a world of possibilities within chemistry. As one chemist aptly put it, “The beauty of molecules lies in their ability to tell us a story about our materials and our world.”

Synonyms
4-METHYLCYCLOHEXANOL
589-91-3
4-methylcyclohexan-1-ol
Cyclohexanol, 4-methyl-
1-Methyl-4-cyclohexanol
p-Methylcyclohexanol
1UK9W4X7H9
NSC 3714
NSC-3714
EINECS 209-664-8
AI3-01169
DTXSID0060434
pMethylcyclohexanol
1Methyl4cyclohexanol
pHexahydromethylphenol
4Hexahydromethylphenol
Cyclohexanol, 4methyl
p-Hexahydromethylphenol
4-Hexahydromethylphenol
DTXCID6042498
4Methylcyclohexanol, mixed isomers
209-664-8
trans-4-Methylcyclohexanol
cis-4-Methylcyclohexanol
7731-29-5
7731-28-4
Cyclohexanol, 4-methyl-, trans-
4-methylcyclohexyl alcohol
Cyclohexanol, 4-methyl-, cis-
4-Methylhexalin
Hexahydro-p-cresol
MFCD00001449
MFCD00064171
ZLJ21O6WVR
4-Methylcyclohexanol, cis-
4-Methylcyclohexanol, trans-
JUW70559WV
Trans 4-Methyl cyclohexanol
Cis-4-Methylcyclohexanol98%
EINECS 231-789-1
EINECS 231-790-7
MFCD00064170
4-methyl-1-cyclohexanol
4-Methylcyclohexanol,c&t
UNII-ZLJ21O6WVR
cis-4-Methyl-cyclohexanol
4-methyl-cyclohexan-1-ol
trans-4-methyl-cyclohexanol
UNII-1UK9W4X7H9
UNII-JUW70559WV
SCHEMBL11799
4-Methyl cyclohexanol, cis-
4-Methylcyclohexanol, (E)-
4-Methylcyclohexanol, (Z)-
1-hydroxy-4-methylcyclohexane
SCHEMBL178952
SCHEMBL181159
SCHEMBL441286
4-Methylcyclohexanol cis+trans
trans-4-methylcyclohexan-1-ol
4-Methyl cyclohexanol, trans-
(1r,4r)-4-methylcyclohexanol
(1s,4s)-4-methylcyclohexanol
SCHEMBL7909834
cis-4-Methylcyclohexanol, 98%
BDBM36145
BDBM36193
NSC3714
CHEBI:232315
trans-4-Methylcyclohexanol, 97%
DTXSID301032962
DTXSID701032964
(1r,4r)-4-methylcyclohexan-1-ol
4-METHYLCYCLOHEXANOL (TRANS)
AKOS000119784
AKOS017343697
AKOS025295736
SB66832
SB84127
4-Methylcyclohexanol, cis + trans, 98%
AS-60626
SY043391
DB-056207
DB-056208
DB-072549
CS-0059254
CS-0180937
CS-0180938
M0196
M0353
M0354
NS00022439
NS00081346
NS00081388
4-Methylcyclohexanol,mixture of cis and trans
EN300-19924
4-Methylcyclohexanol (cis- and trans- mixture)
D73186
D91323
A839037
Q2233075
4-Methylcyclohexanol, purum, cis+trans, >=98.0% (GC)
F8880-5214
Z104476106