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Glycine

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Identification
Molecular formula
C2H5NO2
CAS number
56-40-6
IUPAC name
2-(aminomethyleneamino)acetic acid
State
State

At room temperature, glycine is a solid. Due to its crystalline form, it is stable and can be easily weighed and handled.

Melting point (Celsius)
233.00
Melting point (Kelvin)
506.15
Boiling point (Celsius)
233.00
Boiling point (Kelvin)
506.15
General information
Molecular weight
75.07g/mol
Molar mass
75.0670g/mol
Density
1.6070g/cm3
Appearence

Glycine is typically available as a white crystalline solid. It's often in the form of a free-flowing powder that is highly soluble in water, resulting in a colorless solution.

Comment on solubility

Solubility of 2-(aminomethyleneamino)acetic acid

2-(aminomethyleneamino)acetic acid, with the chemical formula C2H5NO2, is a compound that exhibits interesting solubility characteristics. The solubility of a compound is influenced by several factors, including its polarity, hydrogen bonding potential, and the presence of functional groups. In the case of this amino acid derivative:

  • Polarity: The presence of both amino and carboxylic acid groups contributes to the overall polarity of the molecule, enhancing its ability to interact with polar solvents like water.
  • Hydrogen Bonding: The compound can engage in multiple hydrogen bonding interactions due to its amino and carboxylic acid functionalities, which significantly increases solubility in aqueous solutions.
  • pH Dependence: The solubility of 2-(aminomethyleneamino)acetic acid can vary with pH, as the carboxylic acid group may lose a proton in basic conditions, leading to increased solubility.

Generally, 2-(aminomethyleneamino)acetic acid is likely to be soluble in water, which is characteristic for many amino acids and their derivatives. This solubility enables it to participate in various biochemical reactions and makes it valuable in laboratory and industrial applications.

Interesting facts

Interesting Facts about 2-(Aminomethyleneamino)acetic Acid

2-(Aminomethyleneamino)acetic acid, also known as aminomethylene glycine, is a fascinating compound with unique properties and applications in various fields of science. Here are some intriguing facts:

  • Structure: This compound features two amine groups which contribute to its fascinating reactivity and potential interactions in biological systems.
  • Role in Biochemistry: It is classified as a beta-amino acid, which are known to play crucial roles in several metabolic pathways and may influence protein structure.
  • Research Interest: Scientists are interested in its potential use as a precursor in the synthesis of biomolecules or pharmaceuticals, due to its structural similarities to amino acids.
  • Potential Therapeutic Applications: Some studies suggest the compound has implications in developing novel therapies for various diseases, including certain neurological disorders.
  • Hydrogen Bonding: The presence of multiple amino groups allows for strong **hydrogen bonding**, which may lead to interesting interactions with proteins and other biomolecules.
  • Environmental Impact: Understanding compounds like this one enhances our knowledge of nitrogen cycles in environmental chemistry, especially relating to organic nitrogen compounds.

The intriguing nature of 2-(aminomethyleneamino)acetic acid serves as a reminder of the complex interactions that simple molecules can have in biological systems and their potential applications in human health and environmental sciences.

Synonyms
Formiminoglycine
N-Formimidoylglycine
2140-03-6
Glycine, N-(iminomethyl)-
N-(iminomethyl)glycine
2-Formimidamidoacetic acid
N-Formiminoglycine
2-(aminomethylideneamino)acetic acid
A2GX98A1GX
[(iminomethyl)amino]acetic acid
NSC-90354
formimidoylglycine
(Iminomethyl)glycine
UNII-A2GX98A1GX
SCHEMBL1146702
GLYCINE, N-FORMIMIDOYL-
CHEBI:18415
DTXSID60175667
NSC90354
NSC 90354
AKOS006275064
C02718
Q27103064