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Creatine

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Identification
Molecular formula
C4H9N3O2
CAS number
57-00-1
IUPAC name
1-(diaminomethylene)-2-isobutyl-guanidine
State
State

At room temperature, creatine is a solid compound. It is stable when kept dry and stored away from light and high temperatures.

Melting point (Celsius)
255.00
Melting point (Kelvin)
528.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
131.13g/mol
Molar mass
131.1330g/mol
Density
1.4820g/cm3
Appearence

Creatine is typically found as a white, crystalline powder, which is odorless. It is often used in supplement form and readily dissolves in water, forming a clear solution.

Comment on solubility

Solubility of 1-(Diaminomethylene)-2-isobutyl-guanidine

1-(Diaminomethylene)-2-isobutyl-guanidine is a compound that presents unique solubility characteristics due to its complex structure. Understanding its solubility properties is crucial for practical applications in various chemical processes. Here are some key points about its solubility:

  • Solvent Compatibility: This compound tends to be soluble in polar solvents such as water, owing to its guanidine functional group which can engage in hydrogen bonding.
  • Insolubility in Non-Polar Solvents: Conversely, 1-(diaminomethylene)-2-isobutyl-guanidine shows poor solubility in non-polar solvents. This results from the lack of significant interactions between the compound and non-polar mediums.
  • pH Dependence: The solubility might also vary with pH. Under highly acidic or basic conditions, the compound could experience protonation or deprotonation, enhancing its solubility in aqueous environments.
  • Temperature Influence: Increasing temperature typically enhances solubility for many compounds, and while this may apply to 1-(diaminomethylene)-2-isobutyl-guanidine, specific data is essential for accurate predictions.

In summary, the solubility of 1-(diaminomethylene)-2-isobutyl-guanidine is primarily influenced by the following factors:

  1. Type of solvent used (polar vs. non-polar).
  2. The pH of the solution.
  3. The temperature at which the solubility is measured.

Ultimately, a comprehensive understanding of these solubility characteristics can aid in better applications and integrations of 1-(diaminomethylene)-2-isobutyl-guanidine in various chemical contexts.

Interesting facts

Interesting Facts about 1-(Diaminomethylene)-2-isobutyl-guanidine

1-(Diaminomethylene)-2-isobutyl-guanidine, a compound belonging to the guanidine family, is particularly noteworthy for its diverse applications and intriguing properties. Here are some fascinating points about this compound:

  • Biochemical Importance: This compound can function as a potent agent in biochemical research, often being utilized in studies related to enzyme inhibitors and metabolic pathways.
  • Pharmaceutical Potential: Its structural integrity allows for modifications that may enhance its pharmacological profile, making it a candidate for developing novel therapeutic agents.
  • Amidine Derivative: As a derivative of guanidine, it shares many properties with other amidines, which can have unique interactions with biological systems.
  • Structure-Activity Relationship: Understanding the structural aspects of 1-(diaminomethylene)-2-isobutyl-guanidine can lead to valuable insights in medicinal chemistry, especially in designing more effective drugs.
  • Potential Role in Diabetes Treatment: Certain guanidine derivatives have been researched for their potential in diabetes management, making this compound a candidate for further exploration in metabolic disorders.

"The study of guanidine derivatives often leads to unexpected discoveries in chemistry, highlighting the intricate relationships between molecular structure and biological activity."

This compound exemplifies the intersection of organic chemistry and biochemistry, showcasing how various amine functionalities can influence a compound's reactivity and biological role. The exploration of 1-(diaminomethylene)-2-isobutyl-guanidine not only contributes to our understanding of guanidine-related compounds but also paves the way for innovations in medicinal chemistry.

Synonyms
NSC140880
NSC-140880
i-butylbiguanide
NCGC00014366
NCIStruc1_000168
NCIStruc2_000134
SCHEMBL4100175
CHEMBL1742174
CCG-37806
NCI140880
AKOS017531712
N-isobutyldicarbonimido/ic diamide/imido
NCGC00014366-02
NCGC00097474-01
NCI60_000896