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Glycylglycine

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Identification
Molecular formula
C4H8N2O3
CAS number
556-50-3
IUPAC name
2-[(2-aminoacetyl)amino]acetic acid
State
State
At room temperature, glycylglycine is in a solid state. It is stable under normal temperatures and pressures but should be stored in a well-sealed container to prevent moisture absorption.
Melting point (Celsius)
248.00
Melting point (Kelvin)
521.00
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
132.12g/mol
Molar mass
132.1180g/mol
Density
1.4610g/cm3
Appearence

Glycylglycine appears as a white crystalline powder. It is typically odourless and has a slightly sweet taste. The crystals are often seen as fine, solid particles that reflect light, making them appear glossy or shiny.

Comment on solubility

Solubility of 2-[(2-aminoacetyl)amino]acetic acid

2-[(2-aminoacetyl)amino]acetic acid, often referred to as a derivative of amino acids, exhibits unique solubility properties influenced by its molecular structure. Understanding its solubility is crucial for various applications in biochemical and pharmaceutical fields.

Factors Affecting Solubility

  • Polarity: The presence of amino and carboxyl functional groups significantly enhances its polarity, leading to increased solubility in polar solvents, particularly water.
  • Hydrogen Bonding: The ability to form hydrogen bonds allows for a greater interaction with solvent molecules, promoting dissolution.
  • pH Dependence: The solubility can vary with pH; at acidic pH, protonation may occur, enhancing its solubility, whereas at higher pH values, it may become relatively less soluble.

In general, 2-[(2-aminoacetyl)amino]acetic acid is expected to be highly soluble in water due to its >strong polar characteristics. As a result, it is often utilized in biological studies where aqueous solubility is necessary.

Conclusion

The solubility of this compound, thus, demonstrates a fascinating interplay between its chemical structure and environmental factors, making it a compelling subject for research and application in the chemical sciences.

Interesting facts

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

2-[(2-aminoacetyl)amino]acetic acid, commonly known as *serine*, is an essential amino acid that plays a critical role in numerous biological processes. Below are some intriguing points about this important compound:

  • Biological Significance: Serine is a key building block for protein synthesis, as well as a precursor for the synthesis of various biomolecules such as nucleotides and neurotransmitters.
  • Metabolic Pathways: It is vital in several metabolic pathways, including the synthesis of phospholipids that compose cell membranes, which are crucial for cellular integrity and function.
  • Role in Neurotransmission: Serine plays a pivotal role in the central nervous system, influencing the production of neurotransmitters like dopamine and glycine, which are essential for nerve signaling.
  • Research Applications: Due to its role in metabolism, serine has been a focus of research in areas such as cancer, as cancer cells often have altered serine metabolism.
  • Source of Energy: Under certain conditions, serine can serve as an energy source, being converted into glucose through gluconeogenesis.
  • Historical Discovery: The name “serine” comes from the Latin word “sericum”, meaning silk, due to its initial isolation from silk proteins in the early 19th century.

The diverse roles and benefits of serine highlight its importance not just in human physiology, but also in biochemistry and medicine. As fascinating as it is, ongoing studies are revealing even more about its contributions to health and disease.

Synonyms
Glycylglycine
556-50-3
Diglycine
N-GLYCYLGLYCINE
Glycyl-glycine
Glycine, glycyl-
Glycine dipeptide
Glycyl Glycine
Glycine, N-glycyl-
2-(Aminoacetamido)acetic acid
2-[(2-aminoacetyl)amino]acetic acid
alpha-Glycylglycine
Dipeptide-15
Diglycine (VAN)
[(Aminoacetyl)amino]acetic acid
CHEBI:17201
EINECS 209-127-8
NSC 49346
NSC-49346
GLYCYLGLYCINE [MI]
DIGLYCINE [USP-RS]
AI3-62521
((aminoacetyl)amino)acetic acid
10525P22U0
DTXSID90862194
DIGLYCINE (USP-RS)
GLYGLY
N Glycylglycine
2-((2-azaniumylacetyl)amino)acetate
2-[(2-azaniumylacetyl)amino]acetate
2-((2-aminoacetyl)amino)acetic acid
glycine, glycyl
alphaGlycylglycine
Glycine, Nglycyl
2(Aminoacetamido)acetic acid
DIPEPTIDE-15 [INCI]
DTXCID80197700
2-(glycylamino)acetic acid;hydrochloride
209-127-8
inchi=1/c4h8n2o3/c5-1-3(7)6-2-4(8)9/h1-2,5h2,(h,6,7)(h,8,9
Gly-Gly
2-(2-Aminoacetamido)Acetic Acid
H-Gly-Gly-OH
Gly2
Gly-Gly-OH
MFCD00008130
CHEMBL292467
[(ammonioacetyl)amino]acetate
2-(2-azanylethanoylamino)ethanoic acid
Glycylgycine
UNII-10525P22U0
GG0
H-Gly-Gly
Glycylglycine, DL-
.alpha.-Glycylglycine
n-GLYCYL- Glycine
Glycylglycine (Standard)
Glycylglycine, Free Base
Gly-Gly, 98%
SCHEMBL14934
2-(2-Aminoacetamido)AceticAcid
HY-D0889R
Gly-Gly, >=99% (titration)
[(Aminoacetyl)amino]acetic acid #
HY-D0889
NSC49346
BBL018705
BDBM50169222
s4810
STL194277
AKOS001045997
3-Azapentanoic acid, 5-amino-4-oxo-
CCG-231053
FG40134
Gly-Gly, BioXtra, >=99.0% (NT)
AS-14771
BP-31104
Gly-Gly, BioUltra, >=99.5% (NT)
SY018005
Gly-Gly, Vetec(TM) reagent grade, 99%
DB-002742
CS-0015211
G0124
NS00013721
EN300-34095
C02037
F17229
Q665455
Glycyl-glycine; N-Glycylglycine; Diglycine; Gly-Gly
F2191-0195
33903968-DDB2-47F2-9B6C-7C232D1962DA
Dyglycine, United States Pharmacopeia (USP) Reference Standard
Gly-Gly, BioPerformance Certified, cell culture tested, >=99%
2-[(2-Aminoacetyl)amino]acetic Acid (Diglycine; N-Glycylglycine)