Skip to main content

Hexane-1,3,6-tricarbonitrile

ADVERTISEMENT
Identification
Molecular formula
C9H9N3
CAS number
6297-85-4
IUPAC name
hexane-1,3,6-tricarbonitrile
State
State
Hexane-1,3,6-tricarbonitrile is a liquid at room temperature.
Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.00
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.00
General information
Molecular weight
132.17g/mol
Molar mass
132.1730g/mol
Density
1.0290g/cm3
Appearence

Hexane-1,3,6-tricarbonitrile is a colorless to pale yellow liquid. It may have a faintly acrid odor. Its appearance can be described as clear and typically free from any suspended particles or impurities.

Comment on solubility

Solubility of Hexane-1,3,6-tricarbonitrile

Hexane-1,3,6-tricarbonitrile, with the molecular formula C9H12N6, exhibits notable characteristics regarding its solubility:

  • Non-polar Solvent Preference: Due to its hydrocarbon backbone, hexane-1,3,6-tricarbonitrile is primarily soluble in non-polar solvents. This includes substances like hexane, toluene, and chloroform.
  • Limited Polar Solubility: The presence of cyanide groups does impart some degree of polarity; however, it remains largely insoluble in polar solvents such as water and ethanol.
  • Temperature Influence: Solubility can be affected by temperature, often increasing at higher temperatures, a phenomenon that is typical for many organic compounds.

In summary, when considering the solubility of hexane-1,3,6-tricarbonitrile, it is crucial to remember that non-polar solvents will be its main avenues for dissolution, reflecting its hydrophobic nature.

Interesting facts

Interesting Facts about Hexane-1,3,6-Tricarbonitrile

Hexane-1,3,6-tricarbonitrile is a fascinating compound that belongs to the family of nitriles, which are characterized by the presence of one or more cyano groups (–C≡N). This compound is notable for a variety of reasons:

  • Structural Complexity: With three cyano groups attached to different positions on a hexane chain, hexane-1,3,6-tricarbonitrile is an excellent example of how structural modifications can lead to significant changes in the properties of organic compounds.
  • Use in Synthesis: This compound serves as an important intermediate in organic synthesis. Its multi-cyano structure makes it a useful building block for creating more complex molecules, often used in the fields of pharmaceuticals and materials science.
  • Potential Applications: The presence of cyano groups confers pronounced reactivity, making hexane-1,3,6-tricarbonitrile valuable in producing polymers, agrochemicals, and dyes, among other applications.
  • Environmental Impact: Like many nitriles, the environmental behavior of hexane-1,3,6-tricarbonitrile merits investigation. Its degradation pathways and potential ecological effects are crucial for assessing its safe usage in various industries.

In summary, hexane-1,3,6-tricarbonitrile exemplifies the interplay between structure and reactivity in organic compounds. As highlighted by its varied applications and implications, this compound presents an exciting area for further research and development in chemistry.

Synonyms
1,3,6-Hexanetricarbonitrile
hexane-1,3,6-tricarbonitrile
1,3,6-TRICYANOHEXANE
4-Cyanosuberonitrile
SJY3YNQ3SI
UNII-SJY3YNQ3SI
HSDB 5855
DTXSID4041234
EINECS 217-199-7
DTXCID2021234
1,3,6-TRICYANOHEXANE [HSDB]
4cyanosuberonitrile
1,3,6Hexanetricarbonitrile
un1993
1772-25-4
MFCD00129792
(+/-)-1,3,6-HEXANETRICARBONITRILE, TECH. , 80+%
SCHEMBL1323168
CHEMBL3183751
Tox21_300976
AKOS022182701
s12371
NCGC00248239-01
NCGC00254878-01
BS-21827
CAS-1772-25-4
CS-0198995
H1504
NS00025841
Q27289244