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Ammelide

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Identification
Molecular formula
C3H4N4O
CAS number
645-93-2
IUPAC name
6-amino-1H-1,3,5-triazin-2-one
State
State

At room temperature, ammelide is a crystalline solid.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
369.30
Boiling point (Kelvin)
642.50
General information
Molecular weight
129.10g/mol
Molar mass
129.0990g/mol
Density
2.1520g/cm3
Appearence

Ammelide appears as a colorless crystalline solid.

Comment on solubility

Solubility of 6-amino-1H-1,3,5-triazin-2-one

6-amino-1H-1,3,5-triazin-2-one, often referred to for its interesting properties, exhibits unique solubility characteristics that are vital for its applications in various chemical processes. Understanding the solubility of this compound can be essential for its use in both laboratory and industrial settings.

Key Points Regarding Solubility:

  • Water Solubility: 6-amino-1H-1,3,5-triazin-2-one is known to be soluble in water due to its polar functional groups that facilitate hydrogen bonding with water molecules.
  • Solvent Dependence: The solubility can significantly vary when different solvents are used. It is particularly soluble in solvents like ethanol and methanol, which can be attributed to the polar nature of these organic solvents.
  • Temperature Effects: As with many compounds, solubility in water often increases with temperature. Thus, heating the solution may enhance solubility rates.
  • pH Influence: The solubility can also be affected by pH variations, where alkaline conditions may increase the solubility of basic compounds.

In summary, the solubility of 6-amino-1H-1,3,5-triazin-2-one is influenced by several factors, making it a versatile compound in various chemical reactions. The optimal conditions for achieving desired solubility should be considered for effective use in practical applications.

Interesting facts

Exploring 6-amino-1H-1,3,5-triazin-2-one

6-amino-1H-1,3,5-triazin-2-one is a fascinating compound that belongs to the triazine family, characterized by its unique three-ring structure. This compound is not only significant in the realm of organic chemistry but also has applications that extend into various scientific fields.

Key Characteristics

  • Versatile Building Block: It serves as a versatile building block for synthesizing various organic molecules.
  • Presence in Agriculture: This compound exhibits properties that make it useful in agricultural chemistry, particularly as a precursor in the manufacturing of herbicides.
  • Biochemical Relevance: Its structure resembles certain components found in nucleic acids, showcasing potential implications in biochemical research.

Applications and Significance

The significance of 6-amino-1H-1,3,5-triazin-2-one extends beyond its chemical structure. Some of its intriguing applications include:

  • Pharmaceutical Development: The compound’s unique properties are explored in drug design and the synthesis of pharmaceuticals.
  • Research Tool: Researchers utilize it as a tool to study interactions within biological systems due to its affinity for various biological targets.
  • Material Science: The compound's potential in material synthesis could lead to innovative applications in the field of polymers or nanotechnology.

In summary, 6-amino-1H-1,3,5-triazin-2-one is a compound with diverse applications and a significant role in advancing both theoretical and applied chemistry. As noted by many researchers, “Its intriguing properties continue to inspire new research avenues and discoveries.” Its study not only enhances our understanding of triazine derivatives but also encourages innovation across various chemical disciplines.

Synonyms
5-Azacytosine
931-86-2
1,3,5-Triazin-2(1H)-one, 4-amino-
4-Amino-1,3,5-triazin-2-ol
6-Amino-1,3,5-triazin-2(1H)-one
4-Amino-1,3,5-triazin-2(1H)-one
s-Triazin-2-ol, 4-amino-
s-Triazin-2(1H)-one, 4-amino-
NSC 54006
C5UW4MS7VR
2-Hydroxy-4-aminotriazine
4040-10-2
EINECS 213-242-9
NSC 51100
4-amino-s-triazin-2(1H)-one
CHEBI:72474
UNII-C5UW4MS7VR
NSC-51100
NSC-54006
4-Amino-2-hydroxy-1,3,5-triazine
2-Amino-4-hydroxy-sym-triazine
DTXSID80239275
DTXCID00161766
213-242-9
mfefttygmzoiko-uhfffaoysa-n
5-aza cytosine
6-amino-1H-1,3,5-triazin-2-one
4-Amino-1,3,5-triazin-2-one
2-amino-4-hydroxy-s-triazine
MFCD00006033
CHEMBL1230389
2-Amino-4-hydroxy-1,3,5-triazine
4-amino-1H-1,3,5-triazin-2-one
1118000-83-1
5-Azacytosine-15N4
5-Azacytosine (4-Amino-1,3,5-triazin-2(1H)-one)
MFCD00149402
azacytosine
6-amino-1,2-dihydro-1,3,5-triazin-2-one
5-Aza-Cytosine
5AZ
SCHEMBL13863
SCHEMBL21169645
BCP22914
NSC51100
NSC54006
BDBM50389508
MFCD00051007
4-amino-5H-1,3,5-triazin-2-one
AKOS002658026
AKOS015854832
AKOS015919837
FA05964
4-Methoxy Phencyclidine-d4 Hydrochloride
1216950-61-6
AC-12915
AS-10943
SY030603
4-Amino-1,3,5-triazin-2(1H)-one #
DB-006956
CS-0008471
NS00039530
A51119
EN300-136571
Q27139948
Z1962222528
4-Amino-1,3,5-triazin-2-one;2-Amino-4-hydroxy-S-triazine