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2-Aminooxyacetic acid

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Identification
Molecular formula
C2H5NO3
CAS number
134-93-6
IUPAC name
2-aminooxyacetic acid;carboxymethoxyammonium;chloride
State
State

2-Aminooxyacetic acid is usually encountered as a solid at room temperature.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
91.10g/mol
Molar mass
91.0960g/mol
Density
2.0000g/cm3
Appearence

2-Aminooxyacetic acid typically appears as a white to off-white crystalline powder. It is a solid under standard conditions.

Comment on solubility

Solubility of 2-aminooxyacetic acid; carboxymethoxyammonium; chloride

The solubility of 2-aminooxyacetic acid; carboxymethoxyammonium; chloride is influenced by several factors, primarily due to its ionic nature. Generally, ionic compounds display differing solubility characteristics based on the following factors:

  • Polarity: The presence of polar functional groups in this compound suggests a strong interaction with polar solvents, particularly water.
  • Ionic Strength: Being a chloride salt, it tends to dissolve well in solutions where the ionic strength is balanced. This means that in environments with high ionic strength, solubility may decrease.
  • Temperature: Increased temperature usually enhances the dissolution of many salts. Thus, higher temperatures might increase the solubility of this compound.
  • pH Levels: The protonation state of amino and carboxyl groups can significantly impact solubility. A more acidic environment may lead to higher solubility.

In conclusion, 2-aminooxyacetic acid; carboxymethoxyammonium; chloride is expected to be soluble in water due to its ionic and polar characteristics. However, the exact solubility will depend on the specific conditions outlined above. Understanding these parameters allows for better predictions of solubility in various environments.

Interesting facts

Interesting Facts about 2-Aminooxyacetic Acid; Carboxymethoxyammonium Chloride

2-Aminooxyacetic acid, also known as carboxymethoxyammonium chloride, is a fascinating compound that belongs to the class of organic compounds known as amino acids and their derivatives. This compound presents a unique set of features that make it significant in scientific research. Here are some interesting aspects of this compound:

  • Biological Relevance: 2-Aminooxyacetic acid plays a crucial role in biological processes. Specifically, it acts as an inhibitor of certain enzymes, influencing metabolic pathways and showcasing its potential in pharmaceutical applications.
  • Research Applications: This compound is often used in studies related to neurochemistry and pharmacology, particularly for its effects on neurotransmitter levels in the brain. It provides a valuable tool for investigating neurological disorders.
  • Structural Diversity: The presence of both amino and carboxylate functional groups in this compound allows for interesting interactions with other biological molecules, which can be pivotal in drug design and protein engineering.
  • Safety and Handling: As with any chemical compound, safety protocols must be diligently followed. It is essential to refer to safety data sheets (SDS) when working with this compound to ensure proper handling and minimize any risks.

In summary, 2-aminooxyacetic acid; carboxymethoxyammonium chloride is more than just a chemical entity; it embodies potential solutions to complex biological questions and provides insight into the intricate world of amino compounds. As scientists continue to explore its capabilities, the importance of this compound is likely to grow in the fields of medicine and biochemistry.

Synonyms
(AMINOOXY)ACETIC ACID (AMMONIOOXY)ACETIC ACID CHLORIDE