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3,5-Dimethylcyclohexanol

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Identification
Molecular formula
C8H16O
CAS number
933-48-2
IUPAC name
3,5-dimethylcyclohexanol
State
State

At room temperature, 3,5-Dimethylcyclohexanol is typically a liquid.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.15
Boiling point (Celsius)
202.00
Boiling point (Kelvin)
475.15
General information
Molecular weight
128.21g/mol
Molar mass
128.2140g/mol
Density
0.9112g/cm3
Appearence

3,5-Dimethylcyclohexanol is typically a colorless liquid, although it can appear slightly yellowish depending on purity and storage conditions. It may have a faint, characteristic odor typical of alcohols.

Comment on solubility

Solubility of 3,5-Dimethylcyclohexanol

3,5-Dimethylcyclohexanol, with the chemical formula C10H18O, displays interesting solubility characteristics due to its structural features. This compound is primarily polar because of the hydroxyl (–OH) functional group, which significantly influences its solubility in different solvents.

  • Water: It has limited solubility in water due to its hydrophobic cyclohexane ring, which opposes the water's polarity.
  • Organic Solvents: It shows much greater solubility in organic solvents such as ethanol, ether, and chloroform. The non-polar hydrocarbon part interacts favorably with non-polar solvents.

In summary, 3,5-dimethylcyclohexanol's solubility can be categorized as follows:

  1. Soluble in non-polar organic solvents
  2. Partially soluble in polar solvents like water

This differential solubility can be attributed to its molecular structure, where the balance between polar and non-polar characteristics dictates its interactions with various solvents. Thus, understanding these properties is essential for its applications in chemical reactions and formulations.

Interesting facts

Interesting Facts about 3,5-Dimethylcyclohexanol

3,5-Dimethylcyclohexanol is an intriguing compound that showcases the fascinating world of organic chemistry. Below are some engaging facts about this compound:

  • Structure: The compound features a cyclohexane ring with two methyl groups attached at the 3rd and 5th carbon atoms. This unique arrangement contributes to its chemical properties and potential reactions.
  • Isomerism: Like many organic compounds, 3,5-dimethylcyclohexanol can exist in multiple stereoisomeric forms due to the presence of the methyl groups. This adds complexity and variety to its chemical behavior.
  • Reactivity: As an alcohol, 3,5-dimethylcyclohexanol can participate in various chemical reactions, including dehydration to form alkenes and reactions with acids to create esters.
  • Industrial Applications: While not as widely known as some other alcohols, compounds like 3,5-dimethylcyclohexanol find use in chemical synthesis and may serve as intermediates in the production of more complex compounds.
  • Solvent Properties: This compound may exhibit solvent properties, making it useful in dissolving other organic compounds in laboratory settings.

As a student or professional chemist, understanding and exploring the intricacies of 3,5-dimethylcyclohexanol not only enhances your knowledge of organic chemistry but also opens avenues for practical applications. The study of such compounds is essential in grasping how molecular structure correlates with chemical behavior.

In the words of a famous chemist, "Chemistry is the study of transformation. Every compound tells a story through its structure and interactions." 3,5-Dimethylcyclohexanol is one such compound that embodies this principle!

Synonyms
3,5-DIMETHYLCYCLOHEXANOL
5441-52-1
3,5-Dimethylcyclohexan-1-ol
EINECS 226-630-8
DTXSID20871133
NSC 21130
DTXCID60818805
226-630-8
Cyclohexanol, 3,5-dimethyl-
767-13-5
3.5-Dimethylcyclohexanol
767-14-6
17373-17-0
(1alpha,3alpha,5beta)-3,5-Dimethylcyclohexanol
MFCD00001447
NSC21130
Cyclohexanol,5-dimethyl-
REL-(1S,3R,5S)-3,5-DIMETHYLCYCLOHEXAN-1-OL
3,5-dimethyl-cyclohexanol
(1alpha,3alpha,5alpha)-3,5-Dimethylcyclohexanol
3,5-Dimethylcyclohexanol,c&t
SCHEMBL961521
CHEBI:88850
BCP30899
NSC-21130
AKOS009156899
AB86515
BS-28603
DS-017948
CS-0188357
D0702
NS00044477
3,5-Dimethylcyclohexanol - mixture of isomers
EN300-72416
D89705
(1beta,3alpha,5alpha)-3,5-Dimethylcyclohexanol
1-(1-Adamantyl)-N-(1-naphthylmethyl)ethanamine
Q27160848
5,5-Diethyl-6-methylsulfanyl-5H-pyrimidine-2,4-dione
Z1147526321
(1.alpha.,3.alpha.,5.alpha.)-3,5-Dimethyl-cyclohexanol
(1.alpha.,3.alpha.,5.beta.)-3,5-Dimethyl-cyclohexanol
(1.beta.,3.alpha.,5.alpha.)-3,5-Dimethyl-cyclohexanol
5,5-Diethyl-3-methyl-6-methylimino-dihydro-pyrimidine-2,4-dione
4-(1,3-Benzodioxol-5-yl)-1-(3-chlorophenyl)-3-phenoxy-2-azetidinone
(6Z)-5,5-Diethyl-3-methyl-6-[(Z)-methylimino]dihydro-2,4(1H,3H)-pyrimidinedione
Cyclohexanol, 3,5-dimethyl-;3,5-Dimethylcyclohexan-1-ol;Hexahydro-M-5-Xylenol
4-(4-Hydroxy-phenyl)-1-(tetrahydro-furan-2-ylmethyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid dimethyl ester
Dimethyl 4-(4-hydroxyphenyl)-1-(tetrahydro-2-furanylmethyl)-1,4-dihydro-3,5-pyridinedicarboxylate