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2,6-Diisopropylnaphthalene

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Identification
Molecular formula
C16H20
CAS number
24157-81-1
IUPAC name
2,6-diisopropylnaphthalene
State
State

At room temperature, 2,6-Diisopropylnaphthalene is in a liquid state.

Melting point (Celsius)
21.60
Melting point (Kelvin)
294.75
Boiling point (Celsius)
304.00
Boiling point (Kelvin)
577.15
General information
Molecular weight
212.33g/mol
Molar mass
210.3300g/mol
Density
0.9707g/cm3
Appearence

2,6-Diisopropylnaphthalene is a colorless liquid that appears similar to other hydrocarbon compounds. It does not have any distinct color, and it's usually found in a clear state.

Comment on solubility

Solubility of 2,6-Diisopropylnaphthalene

2,6-Diisopropylnaphthalene, often abbreviated as DIPN, is a polycyclic aromatic hydrocarbon characterized by its unique structure and properties. When it comes to solubility, DIPN exhibits some interesting traits:

  • Nonpolar Characteristics: Due to its nonpolar structure, 2,6-diisopropylnaphthalene shows limited solubility in polar solvents such as water.
  • Solubility in Organic Solvents: DIPN is more soluble in nonpolar organic solvents, including:
    • Benzene
    • Toluene
    • Hexane
  • Temperature Dependence: Like many organic compounds, the solubility of DIPN can change with temperature. As the temperature increases, its solubility in organic solvents often improves.
  • Impact of Structure: The bulky isopropyl groups can affect how molecules interact, resulting in different solubility properties compared to other naphthalene derivatives.

In summary, while 2,6-diisopropylnaphthalene is poorly soluble in aqueous environments, it exhibits significant solubility in various nonpolar organic solvents. This property makes it useful in specific industrial applications where organic solvents are prevalent.

Interesting facts

Interesting Facts about 2,6-Diisopropylnaphthalene

2,6-Diisopropylnaphthalene is an intriguing aromatic hydrocarbon that belongs to the naphthalene family. Here are some fascinating aspects of this compound:

  • Structural Uniqueness: This compound consists of a naphthalene base structure with two isopropyl groups located at the 2 and 6 positions. This unique substitution pattern significantly influences its chemical properties and reactivity.
  • Industrial Applications: It is widely used as a high-performance solvent and is employed in the production of pigments, synthetic fragrances, and even certain types of dyes.
  • Research Interest: Scientists are particularly interested in 2,6-diisopropylnaphthalene due to its potential applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic solar cells, where aromatic compounds are crucial for charge transport.
  • Environmental Considerations: With increasing awareness of environmental preservation, research into the biodegradation of 2,6-diisopropylnaphthalene is gaining traction. Understanding its interactions in ecological systems is essential for assessing its environmental impact.
  • Physical Properties: Though various physical properties like density and boiling point are not discussed here, they play a crucial role in determining how this compound behaves in various conditions, including its volatility and miscibility with other solvents.

The compound stands out not only for its structural aspects but also for its wide-ranging applications and research implications. As scientists continue to explore its potential, 2,6-diisopropylnaphthalene represents a remarkable intersection of chemistry and innovation.

Synonyms
2,6-DIISOPROPYLNAPHTHALENE
24157-81-1
Naphthalene, 2,6-bis(1-methylethyl)-
2,6-DIPN
2,6-Bis(1-methylethyl)naphthalene
Naphthalene, 2,6-diisopropyl-
DTXSID7035272
1X71YEU9QB
NSC-166467
DTXCID5015272
CHEBI:145669
2,6-disopropylnaphtalene
RefChem:83260
246-045-1
2,6-di(propan-2-yl)naphthalene
2,6-Di-iso-propylnaphthalene
MFCD00021648
EINECS 246-045-1
UNII-1X71YEU9QB
EPA Pesticide Chemical Code 055803
NSC 166467
Amplify
NSC166467
Naphthalene,6-diisopropyl-
2,6-diisopropyl naphthalene
SCHEMBL181347
2,6-bis(methylethyl)naphthalene
CHEMBL3182870
SCHEMBL30031337
Naphthalene,6-bis(1-methylethyl)-
Tox21_301083
DIISOPROPYLNAPHTHALENE, 2,6-
AKOS015838375
CS-W014993
FD62592
2,6-Diisopropylnaphthalene, AldrichCPR
NCGC00163959-01
NCGC00163959-02
NCGC00254984-01
AS-40344
SY009039
CAS-24157-81-1
D1598
NS00010761
ST50405143
F341830
Q424809