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Caffeine

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Identification
Molecular formula
C8H10N4O2
CAS number
58-08-2
IUPAC name
N,N-dimethyl-7H-purin-6-amine
State
State

Caffeine is typically found as 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
194.1900g/mol
Density
1.2300g/cm3
Appearence

Caffeine appears as a white, odorless, crystalline powder with a bitter taste.

Comment on solubility

Solubility of N,N-dimethyl-7H-purin-6-amine (C8H10N4O2)

N,N-dimethyl-7H-purin-6-amine, a derivative of purine, exhibits interesting solubility characteristics due to its unique molecular structure. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of amine and carbonyl groups in the structure tends to increase the compound's polarity, which can lead to better solubility in polar solvents.
  • Solvent Type: It is generally more soluble in water and other polar solvents, as opposed to non-polar solvents owing to its hydrophilic nature.
  • pH Level: The solubility can also be pH-dependent; in more acidic or basic conditions, the solubility might increase due to protonation or deprotonation of the amine group.
  • Temperature: As with many compounds, an increase in temperature can enhance solubility, making this compound more soluble at elevated temperatures.

Overall, when considering N,N-dimethyl-7H-purin-6-amine, one can say that it is reasonably soluble in aqueous solutions, making it an interesting candidate for various applications in biochemical research and pharmaceuticals.

Interesting facts

Interesting Facts About N,N-Dimethyl-7H-purin-6-amine

N,N-dimethyl-7H-purin-6-amine, commonly known for its role as a key component in various biological processes, is a fascinating compound with several significant attributes:

  • Biological Significance: This compound is a methylated derivative of adenine, which is a vital nucleobase in the structure of DNA and RNA. Its role in the synthesis of nucleotides is essential for cellular functions.
  • Metabolic Activity: N,N-dimethyl-7H-purin-6-amine is often involved in various metabolic pathways, particularly those related to energy transfer and genetic information transfer in living organisms.
  • Pharmacological Potential: Some studies have indicated that similar purine derivatives are investigated for their potential in therapeutic applications, including anti-cancer and anti-viral activities.
  • Research Utility: Chemists and biochemists employ this compound in research settings to further understand purine metabolism, as well as to develop modified nucleosides that can be used in drug design.
  • Structural Characteristics: The molecular structure of N,N-dimethyl-7H-purin-6-amine features a purine ring system, which is notable for its stability and reactivity, making it a valuable subject of study in organic chemistry.

In the words of a famous chemist, "The exploration of purine analogs continues to unveil new dimensions of biological understanding." This emphasizes the compound's relevance and the exciting research avenues it opens up for scientists worldwide.

Overall, N,N-dimethyl-7H-purin-6-amine is not just a chemical entity; it embodies a wealth of biological and therapeutic significance, making it a noteworthy subject in the field of chemistry.

Synonyms
6-dimethylaminopurine
938-55-6
N,N-dimethyl-7H-purin-6-amine
6-(Dimethylamino)purine
N,N-Dimethyladenine
N6,N6-Dimethyladenine
N(6),N(6)-Dimethyladenine
6-Dimethyladenine
Dimethyladenine
1H-Purin-6-amine, N,N-dimethyl-
Adenine, N,N-dimethyl-
N,N-Dimethyl-9H-purin-6-amine
6,6-Dimethyladenine
n,n-dimethyl-adenine
6-DMAP
N,N-Dimethyl-6-aminopurine
6-(dimethylamino)-Purine
CCRIS 5216
CHEBI:60281
6-Dimethylamino-9H-purine
EINECS 213-344-3
Adenine, N6,N6-dimethyl-
UNII-649SA4S2CV
Purine, 6-(dimethylamino)-
NSC 401568
N(6)-dimethyladenine
6-Dimethylamine purine
N6,N6-dimethyl-Adenine
MFCD00005573
NSC-401568
649SA4S2CV
CHEMBL407391
N,N-dimethyl-1H-purin-6-amine
DTXSID20239658
9H-PURIN-6-AMINE, N,N-DIMETHYL-
104245-07-0
Protein Kinase Inhibitor, DMAP
42C
Adenine,N-dimethyl-
Kinome_3442
Purine, 6-dimethylamino
N6,N6 -dimethyladenine
Maybridge3_000221
purine, 6-dimethylamino-
Epitope ID:140948
SCHEMBL152593
PU09
1H-Purin-6-amine,N-dimethyl-
BDBM92422
DTXCID70162149
Dimethyl-(9H-purin-6-yl)-amine
HMS1431K01
6-(Dimethylamino)purine, >=98%
N,N-Dimethyl-9H-purin-6-amine #
BBL036342
MFCD00079113
NSC401568
s6088
STK370033
AKOS005445384
AKOS015850812
AKOS028109175
CS-W010844
DS-6256
FD04709
HY-W010128
IDI1_011608
SY050761
6-(Dimethylamino)purineN,N-Dimethyladenine
D3894
NS00039689
EN300-63840
T71480
Q15632695
N6,N6-Dimethyladenine; N,N-Dimethyl-9H-purin-6-amine
Z1258992637
N6,N6-Dimethyladenine ; N,N-Dimethyl-9H-purin-6-amine