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1,3-Di-sec-butylurea

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Identification
Molecular formula
C9H20N2O
CAS number
3918-73-8
IUPAC name
1,3-disec-butylurea
State
State

At room temperature, 1,3-di-sec-butylurea is typically a solid. It is relatively stable under standard conditions and not highly volatile.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
172.27g/mol
Molar mass
172.2500g/mol
Density
1.0200g/cm3
Appearence

1,3-Di-sec-butylurea is a colorless solid. It may appear as crystalline or granular powder depending on its preparation and processing. It does not exhibit significant odor.

Comment on solubility

Solubility of 1,3-disec-butylurea

1,3-disec-butylurea (C10H22N2O) exhibits particular solubility characteristics that are worthy of consideration. This compound's solubility is influenced by its structure and functional groups, leading to varying behavior in different solvents. Here are some key points regarding its solubility:

  • Polarity: Due to the presence of the urea functional group, 1,3-disec-butylurea has polar characteristics, which can enhance its interaction with polar solvents.
  • Solvent Compatibility: It is more soluble in polar solvents such as water and alcohols compared to non-polar solvents where its solubility is considerably lower.
  • Temperature Dependency: The solubility of 1,3-disec-butylurea may increase with temperature, which is a common trend for many solid solutes.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules aids in its solubility in aqueous solutions.

In summary, while 1,3-disec-butylurea may exhibit limited solubility in non-polar solvents, its polar nature allows it to dissolve more readily in polar solvents, particularly water. Understanding these solubility properties is essential for applications in chemical processes and formulations.

Interesting facts

Interesting Facts about 1,3-disec-butylurea

1,3-disec-butylurea is a fascinating chemical compound known for its interesting structural characteristics and applications in various fields. As a urea derivative, it is formed by the reaction of isocyanates with amines, specifically employing di-sec-butyl amine. Here are some notable aspects of 1,3-disec-butylurea:

  • Unique Structure: This compound features a distinctive arrangement of isobutyl chains, which influences its physical and chemical properties. The branched nature of the substituents plays a crucial role in its interactions and reactivity.
  • Biological Activity: Research has shown that urea derivatives can exhibit significant biological activity, including potential uses in pharmaceuticals. The potential therapeutic applications of 1,3-disec-butylurea make it an exciting subject for further investigation.
  • Versatile Applications: Beyond its medicinal prospects, this compound may have applications in diverse areas, such as:
    • As a solvent in organic synthesis.
    • In the preparation of advanced materials and polymers.
    • As a potential inhibitor in biochemical reactions.
  • Research Potential: The compound is an excellent candidate for studies aimed at understanding the mechanisms of urea-based interactions, including hydrogen bonding and solubility phenomena.

In summary, 1,3-disec-butylurea stands at the intersection of chemistry and potential biological applications, making it a valuable compound for both research and industrial purposes. As scientists continue to explore its multifaceted properties, the full scope of its utility remains an exciting area of discovery.

Synonyms
DI-SEC-BUTYLUREA
869-79-4
1,3-di-sec-butylurea
SCHEMBL1276559
DTXSID901007179
N,N'-Dibutan-2-ylcarbamimidic acid
AKOS029614218