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Creatine

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Identification
Molecular formula
C4H9N3O2
CAS number
57-00-1
IUPAC name
2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid
State
State
Solid. Creatine is stable under normal temperatures and pressures.
Melting point (Celsius)
292.00
Melting point (Kelvin)
565.00
Boiling point (Celsius)
515.60
Boiling point (Kelvin)
788.80
General information
Molecular weight
131.13g/mol
Molar mass
131.1330g/mol
Density
1.3000g/cm3
Appearence
Creatine appears as a white, crystalline powder. It is odorless and has a slightly acidic taste.
Comment on solubility

Solubility of 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid

The compound 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid, with the chemical formula C4H9N3O2, exhibits interesting solubility characteristics that can be attributed to its polar functional groups.

Key Points on Solubility

  • Hydrophilicity: Due to the presence of amino and carboxylic acid groups, this compound is expected to be highly soluble in water.
  • Solvent Interaction: It may also show better solubility in polar organic solvents due to its ability to form hydrogen bonds.
  • Temperature Dependence: Like many amino acids and their derivatives, the solubility can increase with rising temperature.

The solubility of 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid can also be influenced by:

  1. The pH of the solution, as the ionization state of the amino and carboxylic groups can alter solubility.
  2. Concentration levels in solution, where exceeding saturation can lead to precipitation.

In conclusion, the solubility of 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid is characterized by its ability to dissolve readily in aqueous environments, making it a favorable choice for various biochemical applications.

Interesting facts

Interesting Facts about 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid

2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid, also known as a derivative of imidazole, presents a fascinating intersection of biochemistry and pharmacology. This compound's structural features enable it to play crucial roles in various biological systems.

Key Features and Applications:

  • Amino Acids Connection: The compound contains an amino acid moiety which can impart various biological functionalities such as protein synthesis and enzyme catalysis.
  • Potential as a Drug Candidate: Due to its imidazole ring, it has been investigated for roles in medicinal chemistry, with potential applications in treating various diseases, including certain cancers.
  • pH-Dependent Behavior: The presence of both carboxylic acid and amino groups allows this compound to exhibit interesting behavior under different pH conditions, making it useful in buffer solutions.

Furthermore, its similarity to the essential amino acid glycine suggests that it could play a significant role in cellular processes, particularly in neurotransmission and metabolic pathways.

Biochemical Significance:

In the words of one of the prominent biochemists, "The intricacies of amino-acid-based compounds are pivotal in understanding life's molecular machinery." This compound exemplifies such intricacies by potentially influencing:

  • Protein interactions
  • Metabolic regulation
  • Signal transduction pathways

In summary, 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid embodies a unique intersection of structure and function in biochemical processes. Its potential applications in various fields present exciting avenues for further research and exploration.

Synonyms
cyclocreatine
35404-50-3
1-Carboxymethyl-2-iminoimidazolidine
2-(2-Iminoimidazolidin-1-yl)acetic acid
2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid
1H-Imidazole-1-aceticacid, 2-amino-4,5-dihydro-
2-Imino-1-imidazolidineacetic acid
UNII-6732XGX1RK
6732XGX1RK
AM 285
AM-285
NSC-707961
DTXSID70188889
NSC 707961
1-CARBOXYMETHYL-2-IMINO-IMIDAZOLIDINE
2-(2-amino-4,5-dihydro-1H-imidazol-1-yl)acetic acid
1H-Imidazole-1-acetic acid, 2-amino-4,5-dihydro-
(2-iminoimidazolidin-1-yl)acetic acid
Spectrum_001489
Spectrum2_000925
Spectrum3_001506
Spectrum4_000329
Spectrum5_000997
BSPBio_003151
KBioGR_000677
KBioSS_001969
DivK1c_000483
SCHEMBL450343
SPECTRUM1502085
SPBio_000830
CHEMBL179900
GTPL5491
HMS501I05
KBio1_000483
KBio2_001969
KBio2_004537
KBio2_007105
KBio3_002651
DTXCID80111380
CHEBI:229254
NINDS_000483
HMS1921J06
CCG-39671
MFCD00134455
NSC707961
STL371238
AKOS006222081
AKOS015912660
CS-W018256
FC66337
HY-W017540
1H-Imidazole-1-acetic acid,5-dihydro-
2-(2-Iminoimidazolidin-1-yl)aceticacid
IDI1_000483
NCGC00094958-01
NCGC00094958-02
NCGC00094958-03
AS-37200
NCI60_038283
2-Imino-1-imidazolidineacetic acid, 98%
DB-048796
EN300-7422282
(2-Amino-4,5-dihydro-imidazol-1-yl)-acetic acid
1-carboxymethyl-2-iminoimidazolidine; cyclocreatie
BRD-K14379200-001-04-7
Q27076942