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Dihexyl fumarate

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Identification
Molecular formula
C16H28O4
CAS number
2917-67-5
IUPAC name
dihexyl but-2-enedioate
State
State

At room temperature, dihexyl fumarate is in a liquid state. It remains fluid and easy to pour under normal atmospheric conditions.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
338.10
Boiling point (Kelvin)
611.25
General information
Molecular weight
284.39g/mol
Molar mass
298.4500g/mol
Density
0.9535g/cm3
Appearence

Dihexyl fumarate is a colorless liquid. It is clear and transparent under normal conditions without any visible impurities or coloration.

Comment on solubility

Solubility of Dihexyl But-2-enedioate

Dihexyl but-2-enedioate, with the chemical formula C12H22O4, is a compound that exhibits notable solubility characteristics influenced by its molecular structure.

As an ester, dihexyl but-2-enedioate tends to be soluble in a variety of organic solvents due to the presence of hydrophobic hydrocarbon chains. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound typically shows good solubility in non-polar solvents such as hexane and toluene, which is common for many esters.
  • Limited Water Solubility: It is generally considered to be insoluble in water. The significant hydrophobic sections of the molecule hinder interactions with polar water molecules.
  • Temperature Effects: Solubility may also be affected by temperature, where an increase in temperature can enhance solubility in non-polar solvents.

Overall, dihexyl but-2-enedioate's solubility profile illustrates the general behavior of esters, demonstrating its ability to dissolve in organic media while remaining largely insoluble in aqueous environments. As a result, it can be utilized effectively in various organic applications.

Interesting facts

Interesting Facts about Dihexyl But-2-enedioate

Dihexyl but-2-enedioate is a fascinating compound that belongs to the category of diesters, characterized by its two hexyl groups linked to a butenedioate structure. As a chemical scientist, there are various intriguing aspects of this compound worth considering:

  • Source of Versatility: Dihexyl but-2-enedioate exhibits remarkable versatility, making it useful in a variety of applications ranging from plasticizers to intermediate chemicals in organic synthesis.
  • Biocompatibility: The compound is noted for its biocompatible properties, which makes it a candidate for specific applications in pharmaceuticals and medical devices.
  • Chemical Stability: This compound showcases significant chemical stability, rendering it suitable for diverse environmental conditions, which is crucial in industrial applications.
  • Polymer Industry Demand: The importance of dihexyl but-2-enedioate is notably felt in the polymer industry, where it's sought after as a plasticizer, aiding in enhancing the flexibility and workability of various materials.

In the words of renowned chemist "Innovation in chemistry often stems from understanding the small building blocks of nature." This is particularly true for dihexyl but-2-enedioate, where its structural composition allows chemists to explore innovative solutions in materials science.

Also noteworthy is the compound’s role in creating copolymers, demonstrating how the integration of different monomers can lead to new properties and functions in materials. Its study invites chemists and researchers alike to delve into the realms of organic synthesis and material design.

In conclusion, dihexyl but-2-enedioate presents exciting opportunities for exploration in both practical applications and fundamental research, confirming its status as a compound of interest. Understanding and leveraging its properties may lead to advancements in various fields, including polymer science and medicinal chemistry.

Synonyms
dihexyl but-2-enedioate
maleic acid dihexyl ester
SCHEMBL42964
DTXSID50864659
AKOS030241681
DB-080844