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TES (N-(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl) ethylenediamine-N,N,N',N'-tetraacetic acid)

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Identification
Molecular formula
C6H15NO6S
CAS number
7365-44-8
IUPAC name
2-[[4-[3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxy-tetrahydropyran-2-yl]oxy-5-(hydroxymethyl)pyrrolidin-1-ium-2-carbonyl]amino]ethanesulfonic acid
State
State

TES is typically a solid at room temperature, appearing in its stable crystalline form.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
229.26g/mol
Molar mass
229.2600g/mol
Density
1.5277g/cm3
Appearence

TES is a white crystalline powder. It is highly soluble in water and can form clear solutions. It is known for its buffering capacity in biological and chemical research.

Comment on solubility

Solubility of 2-[[4-[3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxy-tetrahydropyran-2-yl]oxy-5-(hydroxymethyl)pyrrolidin-1-ium-2-carbonyl]amino]ethanesulfonic acid

The compound 2-[[4-[3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxy-tetrahydropyran-2-yl]oxy-5-(hydroxymethyl)pyrrolidin-1-ium-2-carbonyl]amino]ethanesulfonic acid, with the chemical formula C6H15NO6S, exhibits notable solubility characteristics, primarily influenced by its functional groups and ionic nature.

Due to the presence of sulfonic acid groups (-SO3H), this compound is expected to be highly soluble in polar solvents such as water. The key points of its solubility include:

  • Hydrophilicity: The sulfonate group significantly increases the water solubility due to its ability to form favorable interactions with water molecules.
  • Amide and Hydroxy Groups: These functional groups contribute to hydrogen bonding, enhancing solubility in aqueous environments.
  • Ionic Interactions: The presence of positive charge in the pyrrolidinium structure increases solubility since cationic compounds tend to interact more favorably with water.

Overall, the compound is likely to be soluble or at least have high affinity in aqueous solutions, making it suitable for various applications in biological and chemical contexts.

Interesting facts

Interesting Facts about 2-[[4-[3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxy-tetrahydropyran-2-yl]oxy-5-(hydroxymethyl)pyrrolidin-1-ium-2-carbonyl]amino]ethanesulfonic acid

This compound, often referred to by its systematic name, is part of a diverse class of chemical entities known as biological buffers. Buffers are critical in various biochemical applications, maintaining pH levels in biological systems.

Key Characteristics:

  • Buffering Capabilities: This compound plays a significant role in stabilizing the pH of aqueous solutions, which is essential for numerous biological reactions.
  • Biocompatibility: Its unique linkage enables compatibility with cellular systems, reducing the risk of adverse reactions during experimentation.
  • Diverse Applications: Commonly utilized in molecular biology laboratories, this compound aids in enzyme reactions, cell culture, and the preparation of biological assays.

The intricacies of its structure, featuring multiple functional groups such as sulfonic acid, hydroxyl groups, and acetamido moieties, provide it with its distinctive properties. These groups not only confer its buffering capacity but also enhance solubility and interaction with various biomolecules.

Significance in Research:

  • Due to its ability to maintain a stable environment, it is often used in formulations for diagnostic tests and therapeutic applications.
  • The compound’s design allows for targeted modifications, making it an intriguing molecule for chemical synthesis and drug development.

As scientists seek to innovate and improve biochemical techniques, the importance of such compounds cannot be overstated. Overall, 2-[[4-[3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxy-tetrahydropyran-2-yl]oxy-5-(hydroxymethyl)pyrrolidin-1-ium-2-carbonyl]amino]ethanesulfonic acid is a testament to the complexity and utility of modern chemical compounds in advancing our understanding of biological systems.