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tris(2-aminoethyl) borate

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Identification
Molecular formula
C6H18B1N3O3
CAS number
37377-44-5
IUPAC name
tris(2-aminoethyl) borate
State
State

At room temperature, tris(2-aminoethyl) borate is in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
337.00
Boiling point (Kelvin)
610.15
General information
Molecular weight
160.95g/mol
Molar mass
160.9490g/mol
Density
1.0518g/cm3
Appearence

Tris(2-aminoethyl) borate typically appears as a colorless to light-yellow liquid. As a liquid, it is often clear and may have a slightly viscous consistency.

Comment on solubility

Solubility of Tris(2-aminoethyl) Borate

Tris(2-aminoethyl) borate, with its unique chemical structure, exhibits interesting solubility characteristics that can be attributed to its functional groups and polar nature. Understanding its solubility is crucial for applications in various scientific and industrial fields.

Key Solubility Features:

  • Polar Nature: The molecule contains multiple amino groups which enhance its solubility in polar solvents.
  • Water Solubility: Tris(2-aminoethyl) borate is generally soluble in water, allowing for its use in aqueous-based systems.
  • Solvent Compatibility: It shows compatibility with other polar solvents, making it versatile in various chemical reactions.
  • Temperature Dependence: Solubility can vary with temperature; higher temperatures may increase solubility in some solvents.

As noted in scientific literature, compounds similar to tris(2-aminoethyl) borate often demonstrate enhanced solubility profiles due to their functional diversity. To summarize:

  1. Readily soluble in water
  2. Compatible with various polar solvents
  3. Temperature-sensitive solubility

This solubility profile makes tris(2-aminoethyl) borate a valuable chemical for various applications, especially where high solubility is desired.

Interesting facts

Interesting Facts about Tris(2-aminoethyl) Borate

Tris(2-aminoethyl) borate, often referred to as TAB, is a fascinating compound with a variety of applications and unique properties. This compound is a boron-based reagent and is particularly notable due to its role in both organic and inorganic chemistry.

Key Characteristics and Applications:

  • Versatile Reagent: TAB is widely used as a reagent in the synthesis of other chemicals, showcasing its importance in organic synthesis.
  • Complex Formation: This compound can form stable complexes with various metal ions, making it valuable in areas such as catalysis and materials science.
  • Biological Importance: Due to its amine groups, TAB has potential applications in biology, particularly in the modification of biological molecules.
  • Polymer Chemistry: It's employed in polymer chemistry as a crosslinking agent, enhancing the properties of polymer materials.

Furthermore, the structure of tris(2-aminoethyl) borate includes three aminoethyl groups attached to a boron center, which endows it with unique electronic properties. As the American chemist Robert H. Grubbs once stated, "The ability to manipulate and create complex molecules is the heart of chemistry." This sentiment rings true with TAB, as it opens the door to a myriad of synthetic possibilities.

In conclusion, tris(2-aminoethyl) borate exemplifies the intricate interplay between chemistry and practical application, revealing how such a compound can be leveraged across various scientific disciplines.

Synonyms
BORANE, TRIS(2-AMINOETHYL)-
6162-38-5
Tris(2-aminoethyl)borate
BRN 1762110
Ethanol, 2-amino-, triester with boric acid (H3BO3)
AI3-61153
trisaminoethyl borate
3-04-00-00646 (Beilstein Handbook Reference)
SCHEMBL717083
DTXSID10210638