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Alloxan Monohydrate

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Identification
Molecular formula
C4H4N2O4
CAS number
131-58-8
IUPAC name
5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione
State
State

Alloxan monohydrate is typically a solid at room temperature. It is provided in the form of a crystalline powder state.

Melting point (Celsius)
248.00
Melting point (Kelvin)
521.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
186.08g/mol
Molar mass
186.1300g/mol
Density
2.0000g/cm3
Appearence

Alloxan monohydrate typically appears as off-white to light purple, fine crystalline powder. It is hygroscopic, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of 5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione

The compound 5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione displays intriguing solubility characteristics that are noteworthy for researchers and chemists alike. Understanding the solubility of such complex organic molecules can be essential in various applications, including pharmaceuticals and biochemical research.

Factors Affecting Solubility

Several factors can influence the solubility of this compound:

  • Polarity: The presence of multiple hydroxy groups (-OH) suggests that the compound may exhibit moderate polarity, which can enhance solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly improve solubility in polar solvents, supporting interactions with solvent molecules.
  • Molecular Size: The larger molecular structure can hinder solubility in non-polar solvents, where larger compounds are often less soluble.

Soluble Conditions

In general, the solubility profile can be summarized as follows:

  • Water: Likely to be soluble due to the presence of polar functional groups.
  • Organic Solvents: May have limited solubility in non-polar organic solvents.
  • pH Effects: Variations in pH can impact the ionization of functional groups, potentially increasing solubility in acidic or basic conditions.

As a conclusion, while solubility can vary depending on the specific conditions, the presence of numerous hydroxyl groups suggests potential solubility in water, while larger and more complex structures may impose limitations in other solvent systems. Understanding these solubility characteristics is crucial for effective utilization in practical applications.

Interesting facts

Exploring 5-Hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione

5-Hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione is a fascinating chemical compound rich in its potential applications and interesting structural features. This molecule belongs to a class of compounds known as pyrimidines, which are notable for their roles in biological processes. Here are some intriguing points about this compound:

  • Biological Significance: Pyrimidine derivatives often play critical roles in the formation of nucleotides, the building blocks of DNA and RNA. Their presence in biological systems makes understanding their structure and reactions essential in biochemistry.
  • Medicinal Potential: Due to its complex structure, this specific compound may hold promise in pharmaceutical applications. Similar compounds have been explored for anti-cancer, anti-viral, and antibiotic properties.
  • Chemical Reactivity: The unusual presence of multiple hydroxy groups within its framework suggests that it might participate in hydrogen bonding and other interactions that can significantly influence its reactivity.
  • Structural Diversity: The compound displays a unique arrangement of functional groups, making it a subject of interest for chemists seeking to design new molecules with custom functionalities.
  • Research Opportunities: Chemists and researchers are likely to explore its synthesis, as understanding the pathways to create such intricate structures can lead to innovations in material science and drug development.

In conclusion, 5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-hexahydropyrimidin-5-yl)hexahydropyrimidine-2,4,6-trione not only enriches our understanding of pyrimidine chemistry but also provides a platform for future research. As scientists continue to delve into the properties and applications of such compounds, we can expect exciting developments that may impact various fields including medicine and biochemistry.

Synonyms
ALLOXANTIN
76-24-4
Uroxine
Uroxin
ALLOXANTIN, DIHYDRATE
UNII-LTL3CDV62U
LTL3CDV62U
5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-1,3-diazinan-5-yl)-1,3-diazinane-2,4,6-trione
HSDB 2081
5,5'-Bibarbituric acid, 5,5'-dihydroxy-
ALLOXANTIN [MI]
NSC 7634
NSC-7634
EINECS 200-947-1
5,5'-Dihydroxy-5,5'-bibarbituric acid
5,5'-Dihydroxy-5,5'-dibarbituric acid
[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone, 5,5'-dihydroxy-
AI3-23206
DTXSID3058795
NSC7634
NSC-118963
(5,5'-Bipyrimidine)-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone, 5,5'-dihydroxy
(5,5'-Bipyrimidine)-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone, 5,5'-dihydroxy-
Alloxathin
5,5'-DIHYDROXY-(5,5'-BIPYRIMIDINE)-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-HEXONE
5,5'-Dihydroxy-5,5'-bipyrimidinehexaone
5, 5,5'-dihydroxy-
[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-
SCHEMBL137702
DTXCID5047827
MFCD00042797
AKOS024319143
FA01479
A0225
NS00037767
5,5'-Bibarbituric acid, 5,5'-dihydroxy-(8CI)
Q27283170
[5,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone, 5,5'-dihydroxy-
200-947-1