Skip to main content

Pinacolone

ADVERTISEMENT
Identification
Molecular formula
C8H16O
CAS number
75-97-8
IUPAC name
2,2,4,4-tetramethylpentan-3-one
State
State

At room temperature, Pinacolone is in a liquid state.

Melting point (Celsius)
-39.00
Melting point (Kelvin)
234.15
Boiling point (Celsius)
106.30
Boiling point (Kelvin)
379.45
General information
Molecular weight
114.22g/mol
Molar mass
114.1860g/mol
Density
0.8059g/cm3
Appearence

Pinacolone is a colorless liquid with a characteristic spicy or peppermint-like odor. It is typically clear and lacks any visible impurities when pure.

Comment on solubility

Solubility of 2,2,4,4-tetramethylpentan-3-one

2,2,4,4-tetramethylpentan-3-one, with the chemical formula C11H22O, exhibits interesting solubility characteristics.

In general, the solubility of organic compounds like this ketone can be influenced by several factors, including:

  • Molecular structure: The presence of a ketone functional group can enhance solubility in polar solvents.
  • Hydrophobicity: Due to the presence of a large hydrocarbon chain, this compound may exhibit hydrophobic behavior, limiting its solubility in water.
  • Temperature: Solubility often increases with temperature, enabling disintegration in various solvents.

Specifically, it is likely that:

  • 2,2,4,4-tetramethylpentan-3-one is sparingly soluble in water due to its non-polar characteristics.
  • However, it displays good solubility in organic solvents such as ethanol and ethyl acetate.

In conclusion, while 2,2,4,4-tetramethylpentan-3-one prefers non-polar environments, understanding its solubility profile is essential for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 2,2,4,4-Tetramethylpentan-3-one

2,2,4,4-tetramethylpentan-3-one, often referred to as a type of ketone, is recognized for its unique structural properties and applications. This organic compound is intriguing for several reasons:

  • Unique Structure: The presence of four methyl groups attached to the pentan backbone significantly influences its reactivity and physical properties, making it a fascinating subject of study.
  • Industrial Use: It is primarily utilized as an intermediate in organic synthesis, particularly in producing pharmaceuticals and fine chemicals. Its versatility allows it to be a building block for more complex compounds.
  • Odor Characteristics: Like many ketones, 2,2,4,4-tetramethylpentan-3-one possesses distinct odors that are often described as sweet or fruity, which can also be essential in flavor and fragrance formulations.
  • Synthetic Pathways: The synthesis of this compound can involve various methods, including the use of condensation reactions or oxidation techniques, thereby making it an interesting target for organic chemists exploring new synthetic routes.
  • Research Applications: Due to its chemical properties, this ketone has been the subject of multiple studies investigating its behavior under different conditions, enriching our understanding of ketone chemistry.

In summary, 2,2,4,4-tetramethylpentan-3-one is not just a simple organic compound; it carries numerous implications in synthetic chemistry, industrial applications, and sensory characteristics. As such, it provides an exciting opportunity for further exploration in both academic and practical contexts.

Synonyms
815-24-7
2,2,4,4-Tetramethylpentan-3-one
2,2,4,4-TETRAMETHYL-3-PENTANONE
Di-tert-butyl ketone
3-Pentanone, 2,2,4,4-tetramethyl-
AI3-11096
NSC 848
EINECS 212-419-8
DTXSID1061154
DTXCID4048222
212-419-8
inchi=1/c9h18o/c1-8(2,3)7(10)9(4,5)6/h1-6h
Hexamethylacetone
2,2,4,4-Tetramethyl-pentan-3-one
9PW4P959GQ
NSC-848
di-t-butyl ketone
UNII-9PW4P959GQ
SCHEMBL105130
(t-C4H9)2CO
NSC848
2,4,4-Tetramethyl-3-pentanone
3-Pentanone,2,4,4-tetramethyl-
MFCD00008845
AKOS009157034
AS-16106
2,2,4,4-Tetramethyl-3-pentanone, 98%
CS-0132314
NS00038132
EN300-98261
E70342
A840153