Skip to main content

bis(1,3-dimethylbutyl) fumarate

ADVERTISEMENT
Identification
Molecular formula
C16H28O4
CAS number
18758-77-1
IUPAC name
bis(1,3-dimethylbutyl) but-2-enedioate
State
State

At room temperature, bis(1,3-dimethylbutyl) fumarate is in a liquid state. It is often stored in sealed containers to prevent any emission of odorous substances or contamination.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.00
Boiling point (Celsius)
156.00
Boiling point (Kelvin)
429.00
General information
Molecular weight
286.42g/mol
Molar mass
286.4210g/mol
Density
0.9000g/cm3
Appearence
This compound appears as a colorless liquid with a mild, characteristic odor. It is typically clear and free from suspended impurities.
Comment on solubility

Solubility of bis(1,3-dimethylbutyl) but-2-enedioate

Bis(1,3-dimethylbutyl) but-2-enedioate, known for its unique structure and properties, presents an intriguing profile when it comes to solubility.

The solubility of this compound can be influenced by various factors, including:

  • Polarity: The presence of polar functional groups can significantly affect how well the compound dissolves in polar solvents.
  • Temperature: Higher temperatures generally enhance solubility for many organic compounds.
  • Solvent choice: The choice of solvent plays a crucial role; for example, it may dissolve well in organic solvents like dichloromethane or chloroform, whereas it may be poorly soluble in water.

Due to its larger and more complex structure, bis(1,3-dimethylbutyl) but-2-enedioate tends to exhibit lower solubility in aqueous solutions. As similar compounds tend to follow the like dissolves like principle, you might find:

  • Inorganic or polar solvents may not dissolve this compound effectively.
  • Non-polar solvents can provide better solubility outcomes.

In summary, the solubility of bis(1,3-dimethylbutyl) but-2-enedioate is influenced by its structural characteristics, the nature of the solvent, and environmental conditions, leading to a rich field of study for chemists exploring its applications.

Interesting facts

Interesting Facts about Bis(1,3-Dimethylbutyl) But-2-enedioate

Bis(1,3-dimethylbutyl) but-2-enedioate is a fascinating compound that showcases the beauty of organic chemistry and its applications in various fields. This compound belongs to the category of di-esters, specifically characterized by the presence of two but-2-enedioic acid moieties attached to 1,3-dimethylbutyl groups. Here are some intriguing points about this compound:

  • Versatile Building Block: The structure of bis(1,3-dimethylbutyl) but-2-enedioate makes it an excellent intermediate for synthesizing a variety of derivatives that can be utilized in pharmaceuticals, agrochemicals, and materials science.
  • Potential Applications: This compound can be explored for its applications as a plasticizer, which can enhance the flexibility of polymers, making them more suitable for various industrial applications.
  • Synthetic Routes: The synthesis of bis(1,3-dimethylbutyl) but-2-enedioate involves intricate organic reactions, often utilizing nucleophilic acyl substitution techniques. Such reactions highlight the innovative methods chemists employ to build complex organic molecules.
  • Physical Properties: While the specific physical properties of this compound can vary, the presence of ester functionalities often leads to unique characteristics such as distinctive scents and increased volatility.

As stated by prominent chemists, "The beauty of chemistry lies in the ability to create endless possibilities from simple components." Bis(1,3-dimethylbutyl) but-2-enedioate epitomizes this notion by bridging structural chemistry with real-world applications.

In summary, the study of bis(1,3-dimethylbutyl) but-2-enedioate not only enriches our understanding of organic compounds but also opens doors to innovative applications in a multitude of industries. With ongoing research, this compound may very well become a significant player in the future of materials and chemical synthesis.

Synonyms
67953-19-9
Bis(1,3-dimethylbutyl) 2-butenedioate
2-Butenedioic acid, 1,4-bis(1,3-dimethylbutyl) ester
DTXSID30859184
NZQQFMVULBBDSP-UHFFFAOYSA-N
1,4-Bis(1,3-dimethylbutyl) 2-butenedioate
NS00005462