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N-(2-Hydroxyethyl)ethanolamine

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Identification
Molecular formula
C4H11NO2
CAS number
111-42-2
IUPAC name
2-(2-hydroxyethylamino)ethanol;2-(3-iodo-6-methyl-2,4-dioxo-1-piperidyl)acetic acid
State
State

At room temperature, N-(2-Hydroxyethyl)ethanolamine is typically a liquid. It possesses a slightly oily texture and is known for its viscosity compared to water.

Melting point (Celsius)
28.00
Melting point (Kelvin)
301.15
Boiling point (Celsius)
256.00
Boiling point (Kelvin)
529.15
General information
Molecular weight
105.14g/mol
Molar mass
105.1370g/mol
Density
1.1188g/cm3
Appearence

N-(2-Hydroxyethyl)ethanolamine is a colorless to pale yellow viscous liquid. It may exist in an oily form and is typically clear. Due to its hygroscopic nature, it can absorb moisture from the air, which sometimes leads to a change in appearance if exposed for prolonged periods.

Comment on solubility

Solubility Insights for 2-(2-hydroxyethylamino)ethanol

The compound 2-(2-hydroxyethylamino)ethanol (C4H11NO2) exhibits notable characteristics in terms of solubility. This substance is primarily soluble in aqueous solutions, attributed to the presence of both hydroxyl (-OH) and amine (-NH2) functional groups, which enhance its interaction with water molecules.

Factors Influencing Solubility

Several factors contribute to the solubility behavior of 2-(2-hydroxyethylamino)ethanol:

  • Polarity: The polar nature of the hydroxyl and amine groups facilitates hydrogen bonding with water, promoting solubility.
  • Hydrogen Bonding: The ability to form multiple hydrogen bonds increases the stability of the solute in solution.
  • Electrostatic Interactions: The presence of a positively charged amine group can interact favorably with negatively charged species in solution.

As a result, it can be asserted that 2-(2-hydroxyethylamino)ethanol is soluble in water, while its solubility in organic solvents may be limited due to its polar characteristics. This solubility profile plays a vital role in its application in various chemical processes and formulations.

Conclusion

In summary, the solubility of 2-(2-hydroxyethylamino)ethanol in water makes it a versatile compound in many biochemical contexts. Its ability to interact with aqueous environments can be harnessed in pharmaceuticals and other applications, emphasizing the importance of understanding solubility in chemical behavior.

Interesting facts

Interesting Facts About 2-(2-hydroxyethylamino)ethanol

2-(2-hydroxyethylamino)ethanol, commonly referred to as HEA, is a fascinating compound that plays an essential role in various applications, particularly in the field of biochemistry and pharmaceuticals. Here are some noteworthy facts:

  • Biological Significance: HEA is important in the synthesis of neurotransmitters, which are crucial for communication between nerve cells.
  • Versatile Solvent: It is often used as a solvent in hydrophilic solvents due to its ability to dissolve a wide range of polar substances.
  • Amine Functionality: The presence of an amino group enables it to participate in various chemical reactions, making it valuable in organic synthesis.
  • Applications: HEA is utilized in the formulation of personal care products and as a stabilizer in enzyme solutions.

Furthermore, its capacity to act as a mild pH buffer makes it essential in biochemical research, allowing for more controlled experimental conditions. As a student of chemistry, you'll appreciate how HEA exemplifies the interconnectedness of chemical properties and biological applications.

Quote from the Lab

"In every drop of HEA, there's a story of intricate molecular interactions waiting to be unraveled." - Anonymous Chemist


Interesting Facts About 2-(3-iodo-6-methyl-2,4-dioxo-1-piperidyl)acetic acid

This compound is an intriguing example of a complex organic structure with noteworthy properties and potential. Here’s an overview of its unique aspects:

  • Molecular Complexity: It features a unique piperidine ring, which adds to its stability and reactivity, making it a key player in medicinal chemistry.
  • Halogen Chemistry: The incorporation of iodine not only enhances its biological activity but also opens up pathways for various substitution reactions.
  • Potential Therapeutic Applications: Compounds with similar structures are often investigated for their potential as drugs, particularly in treatments related to neurological disorders.
  • Research Interest: Ongoing research focuses on its mechanisms of action and interactions with different biological targets.

As an aspiring chemist, exploring compounds like this can provide insight into the design of novel pharmaceuticals that could change lives. Its intricate design signifies the beauty of organic chemistry, where every atom has a purpose.

Quote to Inspire

"Every molecule holds secrets waiting to be uncovered; keep asking questions." - A Passionate Chemist

Synonyms
(3-Iodo-6-methyl-2,4-dioxopiperidin-1-yl)acetic acid--2,2'-azanediyldi(ethan-1-ol) (1/1)
DTXSID40905808