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2,6-Dimethylheptan-4-one

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Identification
Molecular formula
C9H18O
CAS number
19549-87-2
IUPAC name
2,6-dimethylheptan-4-one
State
State

At room temperature, 2,6-Dimethylheptan-4-one is a liquid. It is not very viscous and flows easily.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
162.00
Boiling point (Kelvin)
435.15
General information
Molecular weight
128.24g/mol
Molar mass
128.2120g/mol
Density
0.8209g/cm3
Appearence

2,6-Dimethylheptan-4-one is a colorless liquid with a characteristic ketone odor. It does not have any distinct color and is typically clear.

Comment on solubility

Solubility of 2,6-dimethylheptan-4-one

The solubility of 2,6-dimethylheptan-4-one can be quite intriguing, primarily due to its unique molecular structure. This compound, a ketone, possesses both hydrophobic and hydrophilic characteristics.

Here are some key points to consider regarding its solubility:

  • Solvent Compatibility: 2,6-dimethylheptan-4-one is generally soluble in organic solvents. It readily dissolves in non-polar solvents such as hexane or chloroform due to its hydrophobic nature.
  • Limited Water Solubility: While this ketone may demonstrate some degree of solubility in water, it is generally considered to have low solubility. This is attributed to its relatively large carbon chain, which hampers hydrogen bonding with water molecules.
  • Temperature Effects: Solubility can also be affected by temperature. As temperature increases, solubility in organic solvents typically improves, while its interaction with water may remain minimal.
  • Molecular Weight Consideration: The molecular weight of 2,6-dimethylheptan-4-one contributes to its physical properties, affecting solubility trends. Generally, larger ketones are less soluble in water compared to their smaller counterparts.

In summary, the solubility of 2,6-dimethylheptan-4-one underscores the complex relationship between structure and solubility behavior in chemical compounds. Understanding these properties is crucial not just in chemical applications but also in predicting how this compound may interact in different environments.

Interesting facts

Interesting Facts about 2,6-Dimethylheptan-4-one

2,6-Dimethylheptan-4-one is a notable compound within the realm of organic chemistry, particularly known for its unique structural and chemical properties. Here are some interesting insights about this fascinating molecule:

  • Functional Group: As a ketone, 2,6-dimethylheptan-4-one contains a carbonyl group (C=O), which plays a critical role in defining its reactivity and interactions with other substances. Ketones are known for their diverse applications in synthesis and as solvents.
  • Isomeric Variance: This compound is a member of the heptanone family, and like many organic compounds, it can exist in several isomeric forms. The spatial arrangement of its atoms leads to different chemical properties, making isomerization a key topic in organic synthesis.
  • Source of Aroma: Compounds like 2,6-dimethylheptan-4-one may also have flavor and fragrance implications. Many ketones contribute pleasant scents, making them useful in the food and perfume industries. This aspect often invites further investigation into their sensory impact.
  • Industrial Relevance: Ketones are widely used in various industries, including pharmaceuticals, agrochemicals, and polymer production. The unique attributes of 2,6-dimethylheptan-4-one may inspire alternative synthesis pathways for creating valuable materials.
  • Research and Development: 2,6-dimethylheptan-4-one often appears in academic research, especially in studies focused on catalysis and organic reactions. Understanding the behavior of such compounds can lead to advancements in chemical methodologies.

In conclusion, 2,6-dimethylheptan-4-one exemplifies the complexity and beauty of organic chemistry. Its varied applications, coupled with an intriguing structure, make it a compound worthy of exploration in both educational and industrial settings.

Synonyms
2,6-Dimethyl-4-heptanone
2,6-Dimethylheptan-4-one
108-83-8
DIISOBUTYL KETONE
Isovalerone
Diisobutylketone
Isobutyl ketone
Valerone
Diisobutilchetone
s-Diisopropylacetone
Di-isobutylcetone
DIBK
4-Heptanone, 2,6-dimethyl-
Diisobutylketon
sym-Diisopropylacetone
2,6-Dimetil-eptan-4-one
sec-Diisopropyl acetone
2,6-Dimethyl-heptan-4-on
2,6-Dimethylheptanone
FEMA No. 3537
NSC 15136
2,6-dimethyl-heptan-4-one
DiisobutylKetone-13C4
Heptanone, 2,6-dimethyl-, 4-
(iso-C4H9)2CO
V52W30H1BU
DTXSID4025080
CHEBI:89195
NSC-15136
2,6-Dimethyl-4-heptanone, tech grade
4-Heptanone,6-dimethyl-
2, GERMAN)
DTXCID905080
Diisobutylketon(DUTCH, GERMAN)
Caswell No. 355B
cognac heptanone
Di-isobutylcetone [French]
Diisobutilchetone [Italian]
CAS-108-83-8
WLN: 1Y1 & 1V1Y1 & 1
CCRIS 6233
HSDB 527
Diisobutylketon [Dutch, German]
EINECS 203-620-1
UN1157
2,6-Dimethyl-4-heptanone (natural)
2,6-Dimetil-eptan-4-one [Italian]
BRN 1743163
UNII-V52W30H1BU
2,6-Dimethyl-heptan-4-on [Dutch,German]
AI3-11270
2,6-Dimethyl-heptan-4-on [Dutch, German]
diisopropylacetone
di-isobutyl ketone
di-iso-butyl ketone
MFCD00008940
EC 203-620-1
2,5-Dimethyl-4-heptanone
Diisobutyl ketone [UN1157] [Flammable liquid]
SCHEMBL36990
4-01-00-03360 (Beilstein Handbook Reference)
SYM-DIISOPROPY LACETONE
2,6 -dimethyl-4 -heptanone
CHEMBL3182186
DIISOBUTYL KETONE [HSDB]
FEMA 3537
2,6-Dimethyl-4-heptanone, 99%
NSC15136
EINECS 271-042-7
Tox21_202406
Tox21_303091
BBL012214
NSC406913
STL163555
2,6-Dimethyl-4-heptanone, >=99%
AKOS005207129
NSC-406913
UN 1157
NCGC00249221-01
NCGC00256951-01
NCGC00259955-01
VS-03235
2,6-DIMETHYL-4-HEPTANONE [FHFI]
2,6-Dimethyl-4-heptanone, technical grade
D0733
NS00009940
2,6-Dimethyl-4-heptanone (diisobutyl ketone)
2,6-Dimethyl-4-heptanone(Diisobutyl Ketone)
EN300-19773
F93016
2,6-Dimethyl-4-heptanone, technical grade, 80%
A801931
Diisobutyl ketone [UN1157] [Flammable liquid]
4-HEPTANONE,2,6-DIMETHYL DIISOBUTYL,KETONE
Q2416556
4-HEPTANONE,2,6-DIMETHYL DIISOBUTYL,KETONE
InChI=1/C9H18O/c1-7(2)5-9(10)6-8(3)4/h7-8H,5-6H2,1-4H
2,6-Dimethylheptan-4-one (sum of 2,6-Dimethyl-4-heptanone & 4,6-Dimethyl-2-heptanone)