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Caffeine

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Identification
Molecular formula
C8H10N4O2
CAS number
58-08-2
IUPAC name
N-cyclopentyl-9-methyl-purin-6-amine
State
State

Caffeine is a solid at room temperature.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
178.00
Boiling point (Kelvin)
451.15
General information
Molecular weight
194.19g/mol
Molar mass
194.1940g/mol
Density
1.2300g/cm3
Appearence

Caffeine appears as a white crystalline solid with a bitter taste.

Comment on solubility

Solubility of N-cyclopentyl-9-methyl-purin-6-amine

N-cyclopentyl-9-methyl-purin-6-amine (C8H10N4O2), a purine derivative, showcases intriguing solubility characteristics. Understanding its solubility is critical for various applications in pharmaceutical formulations and biological systems.

Here are some key points regarding its solubility:

  • Solvent Compatibility: The solubility of this compound is generally favorable in organic solvents as compared to water.
  • Polarity Influence: Being a relatively non-polar molecule due to its cyclopentyl group, its solubility in polar solvents like water is expected to be limited.
  • Hydrogen Bonding: The presence of amine and oxygen functional groups allows potential interactions with solvents that can engage in hydrogen bonding.
  • pH Dependence: The solubility can vary with pH; enhanced solubility may occur in more acidic or basic environments, where protonation or deprotonation effects come into play.

In summary, while N-cyclopentyl-9-methyl-purin-6-amine may exhibit low solubility in water, it is likely to dissolve better in various organic solvents, making its formulation for medicinal use or analytical purposes a noteworthy consideration. As noted, "the right solvent can make all the difference!"

Interesting facts

Interesting Facts about N-cyclopentyl-9-methyl-purin-6-amine

N-cyclopentyl-9-methyl-purin-6-amine, commonly referred to as a member of the purine derivative family, boasts numerous intriguing aspects that capture the attention of scientists and chemistry enthusiasts alike. This compound plays a pivotal role in various fields, most notably in medicinal chemistry and biochemistry.

Key Characteristics

  • Purine Structure: Being a purine derivative, it shares structural similarities with vital biological molecules like nucleotides and nucleic acids, highlighting its potential biological significance.
  • Research Potential: The compound's unique structure opens doors to various research avenues, especially in drug development targeting specific biological pathways.
  • Pharmacological Properties: Compounds with purine-like structures often exhibit a range of pharmacological activities, making them crucial in the development of therapeutics ranging from anti-cancer agents to anti-inflammatory drugs.

Applications in Science

The synthesis and study of N-cyclopentyl-9-methyl-purin-6-amine could lead to breakthroughs in several areas:

  • Antiviral Agents: Research is ongoing to explore its efficacy in combating viral infections, given that purines often play a role in nucleic acid synthesis.
  • Neurological Studies: As a potential modulator, its interaction with certain receptors could shed light on neurological pathways and disorders.
  • Biochemical Probes: It could be utilized in studying purine metabolism and its implications in various diseases, aiding in the development of diagnostic tools.

To summarize, N-cyclopentyl-9-methyl-purin-6-amine represents a fascinating blend of structure and function, showcasing its importance in the vast tapestry of biochemical research. As scientists continue to explore its potential, this compound may reveal more secrets that contribute to our understanding of biological systems and the development of novel therapies. As one noted researcher stated, "The exploration of purine derivatives offers a glimpse into the future of therapeutic innovation."

Synonyms
N6-Cyclopentyl-9-methyladenine
109292-91-3
N-cyclopentyl-9-methylpurin-6-amine
N 0840
N(6)-Cyclopentyl-9-methyladenine
N-0840
CHEMBL48278
9H-Purin-6-amine, N-cyclopentyl-9-methyl-
9H-Purin-6-amine,N-cyclopentyl-9-methyl-
Lopac-N-154
Cyclopentyl-(9-methyl-9H-purin-6-yl)-amine
Lopac0_000921
SCHEMBL1322040
DTXSID60148871
LZMRVYPPUVMKOI-UHFFFAOYSA-N
N6 -Cyclopentyl-9-Methyl Adenine
BDBM50009698
n0840
CCG-205003
NCGC00015717-01
NCGC00015717-02
NCGC00015717-03
NCGC00015717-04
NCGC00094232-01
NCGC00094232-02
NCGC00094232-03
EU-0100921
N-154
L005913
SR-01000075226
SR-01000075226-1
Z990830566