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3,3,5-Trimethylcyclohexanone

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Identification
Molecular formula
C9H16O
CAS number
873-94-9
IUPAC name
3,3,5-trimethylcyclohexanone
State
State

3,3,5-Trimethylcyclohexanone is a liquid at room temperature.

Melting point (Celsius)
-57.60
Melting point (Kelvin)
215.60
Boiling point (Celsius)
206.00
Boiling point (Kelvin)
479.00
General information
Molecular weight
140.23g/mol
Molar mass
140.2270g/mol
Density
0.9107g/cm3
Appearence

3,3,5-Trimethylcyclohexanone is a colorless to pale yellow liquid with a distinctive odor. It is commonly used in organic synthesis and serves as an intermediate for various chemical reactions.

Comment on solubility

Solubility of 3,3,5-Trimethylcyclohexanone

3,3,5-trimethylcyclohexanone, with the molecular formula C12H22O, exhibits interesting solubility characteristics. Its solubility can be influenced by several factors:

  • Polarity: The presence of the carbonyl group (C=O) provides a modest polarity to the compound, which plays a role in its solubility profile.
  • Solvent Interaction: 3,3,5-trimethylcyclohexanone is more soluble in organic solvents such as ethanol, acetone, and other non-polar to mildly polar solvents due to its hydrocarbon structure.
  • Water Solubility: This compound has limited solubility in water, largely due to its non-polar hydrocarbon backbone that restricts interaction with polar water molecules.

In summary, while 3,3,5-trimethylcyclohexanone demonstrates solubility in a range of organic solvents, it is generally insoluble in water, which can be attributed to the competing effects of its hydrophobic structure against the polar characteristics necessary for dissolution in water. Overall, understanding the solubility of this compound is essential for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 3,3,5-Trimethylcyclohexanone

3,3,5-Trimethylcyclohexanone is a unique chemical compound that belongs to the family of ketones, featuring a cyclohexane ring adorned with three methyl groups. This structure contributes to its intriguing properties and applications. Here are some fascinating aspects of this compound:

  • Ketone Class: As a ketone, it is characterized by the presence of a carbonyl group (C=O) which is integral in its reactivity and functionality in chemical reactions.
  • Diverse Applications: This compound is often used in organic synthesis, particularly in the manufacture of fragrances and perfumes due to its pleasant odor. It can also serve as a building block for the synthesis of other more complex organic molecules.
  • Strategic Positioning: The positioning of the methyl groups on the cyclohexane ring allows for various stereochemical configurations. This chirality can impart specific properties to the compound, making it an interesting subject for study in stereochemistry.
  • Industrial Relevance: Its unique structure can provide insights into the development of novel materials and chemicals, playing a role in various industrial applications, particularly in the fields of pharmaceuticals and polymers.
  • Research Potential: The compounds of this type often act as intermediates in synthetic pathways. Researchers may explore their potential for creating new materials with desired characteristics, tapping into the vast landscape of organic chemistry.

The versatility of 3,3,5-trimethylcyclohexanone and its noteworthy reactivity make it a valuable compound for both academic and industrial chemistry. Its role in organic synthesis cannot be understated; who knows what new discoveries await in the realms of chemical research!

Synonyms
3,3,5-TRIMETHYLCYCLOHEXANONE
873-94-9
3,3,5-Trimethylcyclohexan-1-one
Dihydroisophorone
Cyclohexanone, 3,3,5-trimethyl-
EINECS 212-855-9
UNII-QXG9U7N202
QXG9U7N202
DTXSID5044996
AI3-33978
DTXCID3024996
EC 212-855-9
J68.885A
3,3,5-TRIMETHYL-1-CYCLOHEXANONE
3,3,5Trimethylcyclohexan1one
Cyclohexanone, 3,3,5trimethyl
(+-)-3,3,5-trimethylcyclohexanone
(+-)-dihydroisophorone
poswiccrdbkbmh-uhfffaoysa-n
MFCD00019466
(+/-)-DIHYDROISOPHORONE
(+/-)-3,3,5-TRIMETHYLCYCLOHEXANONE
Dihydro-isophorone
3,5,5-trimethyl cyclohexanone
3,5,5-Trimethylcyclohexanone
3,3,5-Trimethyl cyclohexanone
(+/-)-Dihydroisophorone; 3,3,5-Trimethyl-1-cyclohexanone; Dihydroisophorone
SCHEMBL24862
3.3.5-Trimethyl cyclohexanone
CHEMBL3186483
cyclohexanone, 3,3,5-trimethyl
3,3,5-trimethyl-cyclohexan-1-one
AAA87394
IBA49682
Tox21_301727
BBL011400
STL146504
3,3,5-Trimethylcyclohexanone, 98%
AKOS000119271
AKOS016844138
AT10301
PB43658
NCGC00256179-01
CAS-873-94-9
SY051924
VS-02938
DB-056998
NS00008433
T0602
EN300-19037
Q27287551
F0001-2174
Z104472308