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N-Nitrosoglycine

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Identification
Molecular formula
C4H6N2O5
CAS number
3333-64-4
IUPAC name
2-[carboxymethyl(nitroso)amino]acetic acid
State
State

N-Nitrosoglycine is typically a solid at room temperature.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
134.10g/mol
Molar mass
133.0610g/mol
Density
1.5014g/cm3
Appearence

N-Nitrosoglycine appears as a crystalline solid.

Comment on solubility

Solubility of 2-[carboxymethyl(nitroso)amino]acetic acid

2-[carboxymethyl(nitroso)amino]acetic acid, commonly referred to as CAA, demonstrates interesting solubility characteristics:

  • Solubility in Water: CAA is generally soluble in water due to its ionic and polar groups.
  • pH Dependence: The solubility can vary significantly with pH, as the presence of carboxylic acid groups can either donate protons or remain ionized.
  • Temperature Effects: Increased temperature often enhances solubility, as it reduces the viscosity of the solvent.

In summary, the solubility of 2-[carboxymethyl(nitroso)amino]acetic acid is predominantly influenced by its structural characteristics and the surrounding environment. It is vital to consider these factors when handling or utilizing this compound in various applications.

Interesting facts

Interesting Facts about 2-[carboxymethyl(nitroso)amino]acetic acid

2-[carboxymethyl(nitroso)amino]acetic acid, commonly referenced in the scientific community, is a fascinating compound that has captured the interest of chemists and biochemists alike due to its unique structural features and potential applications.

Unique Structural Features

The compound contains several functional groups, including:

  • Carboxymethyl group: This feature enhances its solubility in water and usability in biological systems.
  • Nitroso group: This group adds potential for reactivity and implications in various chemical reactions.

Potential Applications

Research indicates several important domains where 2-[carboxymethyl(nitroso)amino]acetic acid may play a critical role:

  • As a precursor in organic synthesis, enabling the formation of more complex molecules.
  • In bioorganic chemistry, particularly in studying nitrosating agents and their effects in biological systems.
  • In analytical chemistry, it can serve as a reagent for detecting various biological molecules.

Interesting Implications

One of the intriguing aspects of this compound is its potential involvement in biological processes. The nitroso group may have implications in:

  • Cell signaling: Nitroso compounds are known to participate in cellular signaling pathways.
  • Reactivity: The presence of the nitroso group may influence the compound's reactivity with proteins and nucleic acids.

Researchers continue to explore the multifaceted properties of 2-[carboxymethyl(nitroso)amino]acetic acid, making it a compelling subject for ongoing study in both academic and industrial settings.

Synonyms
Nitrosoiminodiacetic acid
25081-31-6
N-Nitrosoiminodiacetic acid
Glycine, N-(carboxymethyl)-N-nitroso-
RRD7T0PY6O
DTXSID5021043
RefChem:164010
DTXCID501043
2-[carboxymethyl(nitroso)amino]acetic acid
ACETIC ACID, NITROSIMINODI-
N-(Carboxymethyl)-N-nitrosoglycine
N-Nitrosoimidodiacetic acid
2,2'-(NITROSOAZANEDIYL)DIACETIC ACID
CCRIS 2612
BRN 1708492
2,2'-(nitrosoimino)diacetic acid
UNII-RRD7T0PY6O
2-[(carboxymethyl)(nitroso)amino]acetic acid
SCHEMBL28309266
XLYVHYXTFHZCNY-UHFFFAOYSA-N
3-Azapentanedioic acid, 3-nitroso-
MFCD01672674
AKOS006279275
AT33250
SY331163
EN300-7690932