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Glycine ethyl ester hydrochloride

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Identification
Molecular formula
C4H9NO2
CAS number
1118-89-4
IUPAC name
(2-aminoacetyl) 2-aminoacetate
State
State

At room temperature, the compound is in a solid state, typically as a white crystalline powder.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.15
Boiling point (Celsius)
226.00
Boiling point (Kelvin)
499.15
General information
Molecular weight
121.14g/mol
Molar mass
121.1360g/mol
Density
1.1900g/cm3
Appearence

The compound appears as a white crystalline powder. It is commonly used in laboratory settings and appears consistent with common crystalline solid structures.

Comment on solubility

Solubility of (2-aminoacetyl) 2-aminoacetate

(2-aminoacetyl) 2-aminoacetate, also known by its systematic name, is a compound that exhibits remarkable solubility properties in various solvents. Its solubility can be influenced by several factors, including:

  • Polarity of the solvent: Being an amino acid derivative, (2-aminoacetyl) 2-aminoacetate is generally soluble in polar solvents such as water and alcohols.
  • Temperature: Solubility typically increases with temperature; therefore, heating the solvent can enhance the dissolution of this compound.
  • pH of the solution: The ionization state of (2-aminoacetyl) 2-aminoacetate changes with pH, affecting its solubility. At lower pH levels, the compound is more protonated and can show increased solubility in acidic environments.

Quoting a well-known principle in chemistry, "like dissolves like," applies here, indicating that the compound will more readily dissolve in solvents that share similar polar characteristics.

Additionally, one should consider the concentration limits: While (2-aminoacetyl) 2-aminoacetate may dissolve well at lower concentrations, higher concentrations could lead to saturation, decreasing its solubility. This compound is highly interactive with water molecules, forming hydrogen bonds that facilitate its dissolution.

In summary, the solubility of (2-aminoacetyl) 2-aminoacetate is predominantly influenced by its polar nature and environmental factors, making it a versatile compound in various aqueous and organic applications.

Interesting facts

Interesting Facts about (2-aminoacetyl) 2-aminoacetate

(2-aminoacetyl) 2-aminoacetate is an intriguing compound that showcases the intersection of amino acid chemistry and synthetic organic processes. This compound serves as a precursor in various biochemical pathways, particularly in the realm of amino acid derivatives and peptides, which are crucial for understanding protein synthesis and function.

Key Characteristics:

  • Biosynthesis: It acts as a key intermediate in the biosynthesis of larger biomolecules.
  • Biological Relevance: This compound is involved in numerous metabolic reactions, highlighting its significance in cellular physiology.
  • Applications: Researchers are exploring its potential applications in pharmaceuticals and agricultural chemicals.

This compound can be thought of as a bridge between simple amino acids and more complex biochemical structures. As a student of chemistry, one may find it fascinating to consider how modifications like the acetylation of amino groups can lead to variations in biological activity. Scientists are continuously evaluating its various properties, and the study of its derivatives can reveal much about enzymatic reactions and their mechanisms.

In the context of synthetic chemistry, compounds such as (2-aminoacetyl) 2-aminoacetate demonstrate how functional groups can be manipulated to create new substances with desirable traits. Understanding the reactivity and stability of this compound can lead to innovative approaches in drug design and synthesis.

Anecdotes from the Lab:

It is often said in the scientific community that "every compound has a story." For (2-aminoacetyl) 2-aminoacetate, the tales of its use in synthesis and its metabolic significance serve as a reminder of the complexity and beauty of chemical interactions.

The exploration of this compound not only enriches our knowledge of organic chemistry but also opens doors to new scientific discoveries, demonstrating the vital role that seemingly simple compounds can play in vast biological systems.

Synonyms
4202-74-8
Glycine, anhydride
Glycine, 1,1'-anhydride
EINECS 224-112-6
Aminoacetic anhydride
(2-aminoacetyl) 2-aminoacetate
2-Aminoacetic anhydride
glycyl glycinate
2-Aminoaceticanhydride
SCHEMBL288431
Glycine, 1,1a(2)-anhydride
DTXSID601313933
AKOS006338219
DB-351680
NS00048987