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p-Isopropylbenzyl alcohol

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Identification
Molecular formula
C10H14O
CAS number
536-66-3
IUPAC name
(4-isopropylphenyl)methanol
State
State

At room temperature, p-Isopropylbenzyl alcohol is typically in a liquid state.

Melting point (Celsius)
21.00
Melting point (Kelvin)
294.15
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2180g/mol
Density
0.9789g/cm3
Appearence

p-Isopropylbenzyl alcohol is a colorless to pale yellow oily liquid. It has a mild pleasant aromatic odor which is often described as a sweet floral scent. This compound is often used in fragrance and flavor industries due to its aromatic properties.

Comment on solubility

Solubility of (4-isopropylphenyl)methanol (C10H14O)

(4-isopropylphenyl)methanol, also known as 4-isopropylbenzyl alcohol, presents interesting solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is expected to be soluble in organic solvents such as ethanol, methanol, and acetone due to its polar hydroxyl group and nonpolar hydrophobic isopropyl group.
  • Water Solubility: The solubility of (4-isopropylphenyl)methanol in water is likely to be quite limited. The hydrophobic character of the isopropyl group can hinder its overall ability to interact favorably with water molecules.
  • Temperature Dependency: As with many organic compounds, solubility may vary with temperature. Increased temperatures generally enhance solubility in organic solvents but may have a lesser effect on water solubility.
  • pH Influence: The solubility could be affected by the pH of the environment, although the presence of a hydroxyl group reduces the likelihood of significant ionization under common conditions.

In summary, while (4-isopropylphenyl)methanol shows promising solubility in organic solvents, its solubility in water is markedly low. Understanding these solubility properties is crucial for applications in synthesis and formulation as they can dictate the behavior of this compound in various environments.

Interesting facts

Exploring (4-Isopropylphenyl)methanol

(4-Isopropylphenyl)methanol, often referred to as a derivative of phenolic compounds, exhibits unique characteristics that make it an intriguing subject of study in organic chemistry. Here are some fascinating facts about this compound:

  • Structure and Substitution: The compound features a benzene ring substituted with an isopropyl group at the para position and a hydroxymethyl group, making it a significant example of a substituted phenol. These substituents impact its physical and chemical properties profoundly.
  • Applications in Synthesis: (4-Isopropylphenyl)methanol serves as a valuable intermediate in the synthesis of various chemical compounds. Its structure allows it to participate in reactions that can lead to more complex organic molecules.
  • Biological Activity: Research has indicated that compounds of this class may exhibit interesting biological activities, including potential anti-inflammatory and analgesic properties. This has sparked interest in examining their medicinal applications.
  • Material Science: Due to its organic nature, (4-Isopropylphenyl)methanol could be explored for roles in developing polymers or materials with tailored properties.
  • Reactivity: The reactivity of the hydroxyl (-OH) group makes (4-Isopropylphenyl)methanol a robust participant in various chemical reactions, including ether formation and esterification, which can be pivotal for synthetic organic chemistry.

The study of (4-Isopropylphenyl)methanol provides insights not just into its properties but also its potential impact in various fields, from pharmaceuticals to material science. As you delve into this compound, remember to consider the broader implications of its chemistry!

Synonyms
4-isopropylbenzyl alcohol
536-60-7
Cumic alcohol
Cuminol
(4-Isopropylphenyl)methanol
cuminyl alcohol
cuminic alcohol
Cumyl alcohol
p-Cymen-7-ol
CUMIN ALCOHOL
p-Isopropylbenzyl alcohol
p-cumic alcohol
Benzenemethanol, 4-(1-methylethyl)-
4-(1-Methylethyl)benzenemethanol
Benzyl alcohol, p-isopropyl-
para-cymen-7-ol
(4-propan-2-ylphenyl)methanol
FEMA No. 2933
p-Cumin-7-ol
[4-(Propan-2-Yl)Phenyl]Methanol
NSC 15672
4-(1-methylethyl)-benzenemethanol
EINECS 208-640-4
p-cymene-7-ol
BRN 0636665
DTXSID0021626
P-Mentha-1,3,5-trien-7-ol
AI3-20440
p-ISOPROPYL BENZYL ALCOHOL
V261W8XR62
4-(1-methylethyl)benzene methanol
MFCD00004663
NSC-15672
CUMIC ALCOHOL [MI]
DTXCID301626
4-ISOPROPYLBENZENEMETHANOL
CHEBI:27628
ISOPROPYLBENZYL ALCOHOL, P-
P-ISOPROPYLBENZYL ALCOHOL [FHFI]
Cuminylalcohol
(4-(propan-2-yl)phenyl)methanol
CAS-536-60-7
UNII-V261W8XR62
p-Cymen-7-ol, 8CI
4-isopropyl-benzyl alcohol
p-Isopropyl-Benzyl alcohol
4-Isopropyl benzyl alcohol
bmse000599
Cuminol ( p-cymen-7-ol)
SCHEMBL113930
(4-Isopropylphenyl)methanol #
WLN: Q1R DY1&1
CHEMBL3183500
4-Isopropylbenzyl alcohol, 97%
FEMA 2933
OIGWAXDAPKFNCQ-UHFFFAOYSA-
HMS1789P06
AAA53660
HY-N7069
NSC15672
Tox21_202025
Tox21_302797
c0376
s5090
AKOS000121600
CCG-266208
CS-W018138
4-(1-Methylethyl)benzenemethanol, 9CI
4-Isopropylbenzyl alcohol, >=97%, FG
NCGC00249151-01
NCGC00256602-01
NCGC00259574-01
AS-59256
DA-62537
I0272
NS00012143
C06576
D97386
Q1143803
Z56347221
InChI=1/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-6,8,11H,7H2,1-2H3
208-640-4