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Aminoguanidine

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Identification
Molecular formula
C8H11N5
CAS number
79-17-4
IUPAC name
1-(diaminomethylene)-2-(2-naphthyl)guanidine
State
State
At room temperature, aminoguanidine is generally found as a solid. It is often stable in its crystalline form and is handled in standard laboratory practice as a solid compound.
Melting point (Celsius)
166.00
Melting point (Kelvin)
439.15
Boiling point (Celsius)
332.00
Boiling point (Kelvin)
605.15
General information
Molecular weight
150.18g/mol
Molar mass
150.1810g/mol
Density
1.7430g/cm3
Appearence

Aminoguanidine typically appears as a white crystalline solid. It may sometimes be a powder, depending on the preparation and processing method. It is often used in its hydrochloride form for stability and ease of handling.

Comment on solubility

Solubility of 1-(diaminomethylene)-2-(2-naphthyl)guanidine

The solubility of 1-(diaminomethylene)-2-(2-naphthyl)guanidine in various solvents can be quite intriguing due to its structural characteristics. Understanding its solubility involves several factors:

  • Polarity: The compound contains both polar and non-polar regions, which influences its solubility in different solvents.
  • Solvent Interaction: It tends to dissolve better in polar solvents like water or alcohols due to its guanidine functional group.
  • Psychoactive Properties: Its interaction with water highlights its potential for biological activity, as solubility may affect bioavailability.
  • Temperature Dependence: Solubility can vary with temperature, often increasing in warmer solvents.

To summarize, the solubility of 1-(diaminomethylene)-2-(2-naphthyl)guanidine is moderate in polar solvents, exhibiting interesting characteristics that can be explored further in various chemical and pharmaceutical applications. Always consider the solvent's properties, as they significantly affect how this compound behaves in solution.

Interesting facts

Discovering 1-(Diaminomethylene)-2-(2-Naphthyl)guanidine

1-(Diaminomethylene)-2-(2-naphthyl)guanidine, an intriguing compound in the field of organic chemistry, exhibits various characteristics that captivate scientists and chemistry enthusiasts alike. This guanidine derivative has gained attention for its potential applications and unique structural properties.

Key Features:

  • Biological Importance: This compound has been investigated for its biological activities, holding promise as a scaffold for the design of new pharmaceutical agents.
  • Structural Complexity: The presence of a naphthyl group contributes significantly to its aromatic characteristics, allowing for possible interactions with various biomolecules.
  • Versatility: The diaminomethylene group endows the compound with basic properties, making it an interesting candidate for studying acid-base reactions and interactions.

Researchers often cite, “The beauty of organic compounds lies not only in their structure but in their potential applications.” This is particularly true for 1-(diaminomethylene)-2-(2-naphthyl)guanidine, where its structural framework can lead to the exploration of novel therapeutic strategies.

Research Applications:

The compound's various aspects can open up discussions in:

  • Medicinal Chemistry: Investigating its role in drug development.
  • Material Science: Analyzing its potential in polymerization processes.
  • Environmental Chemistry: Exploring its interactions and transformations in natural systems.

In conclusion, 1-(diaminomethylene)-2-(2-naphthyl)guanidine represents a fascinating example of organic compounds, with intriguing implications for health and materials chemistry, unlocking avenues for future research and development.

Synonyms
N-2-naphthylimidodicarbonimidic diamide
5426-97-1
DTXSID00274542
DTXCID90226015
1-(diaminomethylidene)-2-naphthalen-2-ylguanidine
2-naphthyl biguanide
CHEMBL43078
MLS000663632
1-CARBAMIMIDAMIDO-N-(NAPHTHALEN-2-YL)METHANIMIDAMIDE
SMR000292786
1215-36-7
beta-Naphtylbiguanid
NSC14445
MFCD03615420
Opera_ID_1723
SCHEMBL7427727
HMS1589N18
HMS2596M12
HMS3380M02
ALBB-022017
BDBM50053617
NSC-14445
STK102821
N-2-naphthylimidodicarbonimidicdiamide
AKOS003745039
NCGC00245669-01
LS-06766
PD129491
N-2-Naphthalenylimidodicarbonimidic diamide
N-naphthalen-2-ylimidodicarbonimidic diamide
CS-0322948
H33352
Imidodicarbonimidic diamide, N-2-naphthalenyl-
2-{[{[AMINO(IMINO)METHYL]AMINO}(IMINO)METHYL]AMINO}NAPHTHALENE