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glycine hydroxamate

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Identification
Molecular formula
C2H5NO3
CAS number
5424-92-8
IUPAC name
2-(hydroxyamino)acetic acid
State
State

At room temperature, glycine hydroxamate is in a solid state.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
91.07g/mol
Molar mass
91.0670g/mol
Density
1.2820g/cm3
Appearence

Glycine hydroxamate typically appears as a solid compound that is white to off-white in color.

Comment on solubility

Solubility of 2-(hydroxyamino)acetic acid

2-(hydroxyamino)acetic acid, a compound characterized by its distinctive structure, exhibits interesting solubility properties. Here are some key points regarding its solubility:

  • Water Solubility: This compound is highly soluble in water due to its ability to form hydrogen bonds with water molecules.
  • Polarity: The presence of both an amine and a hydroxyl group enhances its polarity, which contributes to its solubility in polar solvents.
  • Temperature Dependence: Like many organic compounds, the solubility may increase with temperature, making it more soluble in warm water.

As a general observation, compounds with functional groups such as -OH (hydroxyl) and -NH₂ (amine) typically demonstrate increased solubility in aqueous environments. Therefore, it is not surprising that 2-(hydroxyamino)acetic acid can dissolve readily in water, making it accessible for various applications in chemical and biochemical research.

“Solubility is often a key factor in the utility of a compound, influencing its behavior in biological systems and its application in synthesis.”

Interesting facts

Interesting Facts about 2-(Hydroxyamino)acetic Acid

2-(Hydroxyamino)acetic acid, commonly known as serine, plays an essential role in biochemistry and is one of the 20 standard amino acids used by cells to synthesize proteins. Here are some intriguing aspects of this compound:

  • Building Block of Proteins: As a non-essential amino acid, serine is crucial for various physiological functions, including the synthesis of proteins that are critical for cellular structure and function.
  • Involvement in Enzyme Reactions: Serine is a key player in several enzyme-catalyzed reactions, acting as a site for the transfer of functional groups. Its hydroxyl group enhances its ability to participate in enzymatic activities.
  • Metabolic Pathways: It serves as a precursor for synthesizing other important biomolecules, including the neurochemical serotonin and the nucleotides RNA and DNA.
  • Biological Functions: Beyond protein synthesis, serine is involved in important metabolic processes, such as the conversion of homocysteine to cysteine, which is vital for maintaining a healthy cardiovascular system.
  • Role in Cell Signaling: The presence of serine in proteins can affect the activity of signaling pathways, influencing cellular responses to different stimuli.

In conclusion, 2-(hydroxyamino)acetic acid transcends its humble beginnings as an amino acid to play multifaceted roles in biology and chemistry. As we continue to explore the depths of this essential compound, we discover that its contributions to life are both profound and intricate.

Synonyms
N-Hydroxyglycine
2-(hydroxyamino)acetic acid
(Hydroxyamino)acetic acid
GLYCINE, N-HYDROXY-
Acetic acid, (hydroxyamino)-
FVT2AQ968S
NSC 76386
BRN 1743147
CHEBI:38049
NSC-76386
DTXSID60188959
0-04-00-00542 (Beilstein Handbook Reference)
Hydroxyaminoacetate
Hydroxylamino acetate
DTXCID70111450
(hydroxyamino)acetic acid;N-hydroxyglycine
961-204-1
3545-78-6
Hydroxyaminoacetic acid
Hydroxylamino acetic acid
hydroxyglycine
N-Hydroxy Glycine
N-HYDROXY-GLYCINE
2-(hydroxyamino)aceticacid
UNII-FVT2AQ968S
2-(hydroxyamino)-acetic acid
CHEMBL1645222
NSC76386
AKOS006376625
DS-007834
EN300-103847
Q27117361
Z1205493750