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Creatine

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Identification
Molecular formula
C4H9N3O2
CAS number
57-00-1
IUPAC name
2-[carbamimidoyl(methyl)amino]acetic acid
State
State

Creatine is typically found in a solid state at room temperature. This compound is hygroscopic, meaning it has the ability to absorb moisture from the environment, which might affect its texture over time, often making it slightly clumped rather than powdery.

Melting point (Celsius)
292.00
Melting point (Kelvin)
565.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
131.13g/mol
Molar mass
131.1340g/mol
Density
1.3300g/cm3
Appearence

Creatine usually appears as a white crystalline solid at room temperature. It is typically found in a powdered form, and when viewed closely, it consists of small, fine crystals.

Comment on solubility

Solubility of 2-[carbamimidoyl(methyl)amino]acetic acid (C4H9N3O2)

The solubility of 2-[carbamimidoyl(methyl)amino]acetic acid is a fascinating aspect to delve into, as it highlights the compound's potential applications in various fields. Here are some key points:

  • Polarity: Due to the presence of both amino and carboxylic acid functional groups, this compound exhibits a high degree of polarity, which generally enhances its solubility in polar solvents such as water.
  • pH Dependence: The solubility may be influenced by pH levels. In acidic conditions, the carboxyl group can remain protonated, influencing solubility dynamics.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvent molecules further aids its dissolution, making it more soluble in aqueous solutions compared to non-polar solvents.

In summary, one of the most significant attributes of 2-[carbamimidoyl(methyl)amino]acetic acid is its favorable solubility profile in polar solvents, which is pivotal for its utility in biochemical applications. Understanding these solubility characteristics can greatly enhance its functional role in chemical processes.

Interesting facts

Interesting Facts about 2-[Carbamimidoyl(methyl)amino]acetic Acid

2-[Carbamimidoyl(methyl)amino]acetic acid, a fascinating compound known for its role in biochemical processes, serves as a versatile building block in the synthesis of various molecules. Here are some notable features of this intriguing compound:

  • Biological Significance: This compound is a derivative of amino acids, which are the fundamental building blocks of proteins. Its structure enables it to play a crucial role in biological processes, particularly in metabolic pathways.
  • Synthetic Application: Due to its unique functional groups, 2-[carbamimidoyl(methyl)amino]acetic acid can be used in the synthesis of pharmacologically active compounds. This makes it an essential component in medicinal chemistry.
  • Studies in Enzyme Inhibition: Recent studies have hinted at its potential as a scaffold in the design of enzyme inhibitors, which can lead to new therapeutic agents. Researchers are keen on exploring its efficacy against specific biological targets.
  • Research Developments: The compound's unique properties have led to its investigation in various scientific fields, including drug discovery and agricultural chemistry. Ongoing research aims to develop novel applications, enhancing its utility in both medicine and environmental science.

As noted by prominent chemists, "The potential within seemingly simple compounds like 2-[carbamimidoyl(methyl)amino]acetic acid continues to amaze us, reminding us that complexity often lies beneath the surface." The exploration of this compound and its derivatives is ripe for discovery, paving the way for innovation in numerous sectors.

In summary, 2-[carbamimidoyl(methyl)amino]acetic acid exemplifies the intersection of simplicity and complexity in chemistry, making it an important subject of study in both academic and practical applications.

Synonyms
creatine
57-00-1
Creatin
Kreatin
N-amidinosarcosine
Krebiozon
N-methyl-N-guanylglycine
2-(1-Methylguanidino)acetic acid
methylglycocyamine
Glycine, N-(aminoiminomethyl)-N-methyl-
Creatine, hydrate
Pyrolysate
Creatine, anhydrous
(alpha-Methylguanido)acetic acid
Cosmocair C 100
N-carbamimidoyl-N-methylglycine
2-(1-methylcarbamimidamido)acetic acid
Kreatinum
Neotine
Methylguanidoacetic acid
N-(aminoiminomethyl)-N-methylglycine
alpha-Methylguanidino acetic acid
NSC 8752
NSC-8752
UNII-MU72812GK0
A-MEethyl guanidine acetic acid
CHEBI:16919
AI3-15320
HSDB 7336
MU72812GK0
(.alpha.-Methylguanido)acetic acid
(N-methylcarbamimidamido)acetic acid
EINECS 200-306-6
((amino(imino)methyl)(methyl)amino)acetic acid
MFCD00004282
N-[(E)-AMINO(IMINO)METHYL]-N-METHYLGLYCINE
DTXSID1040451
NSC8752
EC 200-306-6
2-(N-methylcarbamimidamido)acetic acid
N-(Aminoiminomethyl)-N-methyl-glycine
CREATINE (II)
CREATINE [II]
CREATINE (USP-RS)
CREATINE [USP-RS]
(N-(AMIDINO)-N-METHYLAMINO)ACETIC ACID
N-(amino(imino)methyl)-N-methylglycine
N-[amino(imino)methyl]-N-methylglycine
Creatine (8CI)
((amino(imino)methyl)(methyl)amino)acetate
[[Amino(imino)methyl](methyl)amino]acetate
2-[carbamimidoyl(methyl)amino]acetic acid
[[Amino(imino)methyl](methyl)amino]acetic acid
N-((E)-AMINO(IMINO)METHYL)-N-METHYLGLYCINE
Kre-Alkalyn
Methylguanidoacetate
IOM
CREATINE [HSDB]
CREATINE [MI]
CREATINE [VANDF]
bmse000078
bmse000950
bmse000999
CREATINE [WHO-DD]
(alpha-Methylguanido)acetate
(a-Methylguanido)acetic acid
SCHEMBL21567
Creatine, hydrate (Salt/Mix)
CHEMBL283800
GTPL4496
DTXCID9020451
STR05570
BBL012187
BDBM50357229
s5588
STL163516
AKOS005717096
CCG-266112
CS-W011104
DB00148
FC01727
HY-W010388
Creatine, anhydrous, >=99.0% (NT)
NCGC00371407-01
AC-34370
N-Guanyl-N-methylglycine;N-Amidinosarcosine
C3610
NS00009931
C00300
D89574
EN300-1692957
[[Amino(imino)methyl](methyl)amino]acetic acid #
Q223600
BRD-K19615002-001-02-3
F8880-7830
Z1203577925
1093737-19-9
200-306-6