Skip to main content

p-Menth-3-en-1-ol

ADVERTISEMENT
Identification
Molecular formula
C10H18O
CAS number
10482-56-1
IUPAC name
1-isopropyl-4-methyl-cyclohex-3-en-1-ol
State
State

At room temperature, p-Menth-3-en-1-ol is a liquid. The compound is stable under standard conditions and can easily be incorporated into various formulations for industrial and cosmetic use.

Melting point (Celsius)
0.00
Melting point (Kelvin)
273.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2540g/mol
Density
0.9301g/cm3
Appearence

p-Menth-3-en-1-ol, also known as terpineol, is a colorless liquid with a lilac-like odor. It is typically clear and sometimes may appear slightly viscous. It is often used in perfumes and cosmetics due to its pleasant aroma.

Comment on solubility

Solubility of 1-isopropyl-4-methyl-cyclohex-3-en-1-ol

1-isopropyl-4-methyl-cyclohex-3-en-1-ol, a cyclic alcohol, exhibits interesting solubility characteristics that are influenced by its molecular structure. When considering its solubility, the following points can be highlighted:

  • Polarity: The presence of the hydroxyl group (-OH) contributes to some degree of polarity, allowing for potential interactions with polar solvents like water.
  • Hydrophobic Interactions: The bulky isopropyl and methyl groups enhance hydrophobic characteristics, which can diminish solubility in polar solvents.
  • Solvent Compatibility: This compound is more likely to dissolve in organic solvents such as ethanol, methanol, or acetone, due to its non-polar characteristics.
  • Temperature Dependency: Solubility may increase with temperature, as higher temperatures can lead to greater molecular motion, disrupting intermolecular forces.
  • Mixtures: In mixtures with varying solvent compositions, the solubility may vary, presenting unique challenges in applications.

In summary, while 1-isopropyl-4-methyl-cyclohex-3-en-1-ol can exhibit some solubility in polar solvents due to its -OH group, it is predominantly soluble in non-polar organic solvents owing to its hydrophobic regions. Therefore, it is crucial to consider solvent choice for effective applications.

Interesting facts

Interesting Facts About 1-isopropyl-4-methyl-cyclohex-3-en-1-ol

1-isopropyl-4-methyl-cyclohex-3-en-1-ol, often referred to in organic chemistry discussions, showcases the fascinating world of cyclic compounds. Here are some compelling aspects of this unique molecule:

  • Nature of Structure: This compound features a cyclohexene ring, which introduces intriguing properties associated with its unsaturation. The presence of a double bond contributes to its reactivity, making it a candidate for various chemical transformations.
  • Functional Groups: The alcohol (-OH) group and the alkene (C=C) bond provide significant functional versatility, allowing chemists to explore avenues in organic synthesis, including reactions like hydroxylation and addition reactions.
  • Applications in Synthesis: Due to its structure, this compound can be synthesized or utilized in the production of pharmaceuticals, fragrances, and specialty chemicals, highlighting its significance in industrial chemistry.
  • Isomeric Potential: The isopropyl and methyl groups attached to the cyclohexene skeleton present valuable options for stereochemical isomerism, which can influence the biological activity of similar compounds.
  • Environmental Aspects: As a part of the broader category of terpenoids, this compound can also hint at potential applications in green chemistry, being suitable for use in environmentally benign processes.

In the words of famed chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” Investigating the practical applications and synthesis of compounds like 1-isopropyl-4-methyl-cyclohex-3-en-1-ol reflects this sentiment, combining creativity with rigorous scientific inquiry.

Overall, this compound not only exemplifies the complexities of molecular design but also serves as a reminder of the continual exploration in the field of chemistry.

Synonyms
Terpinen-4-ol
4-Carvomenthenol
562-74-3
4-Terpineol
1-Terpinen-4-ol
1-p-Menthen-4-ol
Terpene-4-ol
1-Menthene-4-ol
TERPINENE-4-OL
1-para-Menthen-4-ol
(+-)-p-Menth-1-en-4-ol
Melaleucol
Terpinenolu-4
Terpineol-4
dl-4-Terpineol
FEMA No. 2248
para-Menth-1-en-4-ol
4-Carvomenthenol (natural)
1-Methyl-4-isopropyl-1-cyclohexen-4-ol
4-Methyl-1-isopropyl-3-cyclohexen-1-ol
Terpin-4-en-1-ol
CCRIS 9067
NSC 147749
EINECS 209-235-5
EINECS 248-910-9
UNII-L65MV77ZG6
alpha-terpinen-4-ol
BRN 1906603
L65MV77ZG6
1-isopropyl-4-methylcyclohex-3-en-1-ol
CHEBI:78884
NSC-147749
HSDB 8264
(1)-1-(Isopropyl)-4-methylcyclohex-3-en-1-ol
4-06-00-00250 (Beilstein Handbook Reference)
1-(ISOPROPYL)-4-METHYLCYCLOHEX-3-EN-1-OL
METHYL-1-(1-METHYLETHYL)-3-CYCLOHEXEN-1-OL
209-235-5
(+-)-4-terpineol
(+-)-terpinen-4-ol
4-terpineol, (+-)-
terpinen-4-ol,(+-)-
Terpinenol-4
p-Menth-1-en-4-ol
rac Terpinen-4-ol
3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-
(+/-)-Terpinen-4-ol
4-Methyl-1-(1-methylethyl)-3-cyclohexen-1-ol
Terpinine-4-ol
(+/-)-4-Terpineol
4-methyl-1-propan-2-ylcyclohex-3-en-1-ol
4-Methyl-1-(propan-2-yl)cyclohex-3-en-1-ol
4-TERPINEOL, (+/-)-
MFCD00001562
DTXSID4044824
TERPINEN-4-OL,(+/-)-
L-4-terpineneol
L-4-terpineol
L-terpinen-4-ol
Terpinenolu-4 [Czech]
(+/-)-1-Isopropyl-4-methyl-3-cyclohexen-1-ol
Origanol
(-)-Terpinen-4-ol (contains 30% (+)-Terpinen-4-ol at maximum)
Terpinen 4-ol
rac-Terpinen-4-ol
(-)-1-Isopropyl-4-methyl-3-cyclohexen-1-ol
alpha -Terpinen-4-ol
1-Isopropyl-4-methyl-3-cyclohexen-1-ol, (R)-
1-isopropyl-4-methyl-cyclohex-3-en-1-ol
Terpinen-4-ol (Standard)
SCHEMBL22344
TERPINEN-4-OL [FCC]
(-)-p-Menth-1-en-4-ol
CHEMBL507795
4-CARVOMENTHENOL [FHFI]
DTXCID2024824
FEMA 2248
(+/-)-p-Menth-1-en-4-ol
HY-W017316R
Tox21_301785
AC1341
NSC147749
s6118
AKOS015903412
CS-W018032
DB12816
FT27574
HY-W017316
SB44714
4-Carvomenthenol, >=95%, FCC, FG
NCGC00256250-01
1-Isopropyl-4-methyl-3-cyclohexen-1-ol
4-Carvomenthenol, natural, >=95%, FG
AS-56462
CAS-562-74-3
DA-58415
SY012857
DB-066063
DB-234185
M0319
NS00013199
T1993
C17073
Q416114
(-)-4-Hydroxy-4-isopropyl-1-methyl-1-cyclohexene
(+/-)-4-Hydroxy-4-isopropyl-1-methyl-1-cyclohexene
Terpinen 4-ol, primary pharmaceutical reference standard
4-Methyl-1-(1-methylethyl)-3-cyclohexen-1-ol;p-Menth-1-en-4-ol