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Aminourea

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Identification
Molecular formula
CH5N3O
CAS number
624-08-2
IUPAC name
aminourea
State
State

At room temperature, aminourea exists as a solid. It is stable under standard conditions, although care must be taken to avoid exposure to moisture as it is somewhat hygroscopic.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
75.07g/mol
Molar mass
75.0670g/mol
Density
1.4280g/cm3
Appearence

Aminourea appears as a white crystalline solid. It is a colorless compound under normal conditions and can be handled like other similar crystalline solids. It may absorb moisture or react with water and other solvents, which is typical behavior for many organic solid compounds.

Comment on solubility

Solubility of Aminourea (CH5N3O)

Aminourea is generally known for its moderate solubility in water, making it an interesting compound for various applications in chemical processes and formulations. Its solubility characteristics can be influenced by several factors:

  • Temperature: Increasing the temperature often enhances the solubility of aminourea, allowing for greater dissolution in aqueous solutions.
  • pH Levels: The ionization state of aminourea can vary with changing pH, and this can impact solubility. In more acidic or basic conditions, altered solubility patterns may be observed.
  • Presence of Other Solvents: Aminourea’s solubility can also be affected by the presence of co-solvents or salting agents, which may either promote or inhibit its dissolution in a given medium.

As a nitrogen-containing compound, aminourea exhibits a degree of *hydrophilicity*, contributing to its solubility in water. Such properties pose some significance in the context of bioavailability and reaction kinetics:

  • It can readily engage in **hydrogen bonding**, which favors solvation.
  • Aminourea’s structure allows for a diverse range of interactions, expanding its usefulness in various chemical syntheses.

In summary, while the solubility of aminourea is generally favorable in aqueous environments, variations due to temperature, pH, and solvent composition are pivotal considerations in both laboratory and industrial settings. Understanding these factors helps optimize processes involving this compound.

Interesting facts

Aminourea: An Intriguing Compound

Aminourea, a simple yet fascinating compound, has garnered attention in various fields of chemistry and biology. Here are some compelling facts about this unique substance:

  • Biological Importance: Aminourea is known for its role in biological systems, particularly as a precursor in the synthesis of important biomolecules.
  • Industrial Applications: This compound is utilized in the production of fertilizers, aiding in plant growth by providing essential nitrogen.
  • Research Potential: Scientists are exploring the potential of aminourea in drug synthesis, particularly in developing pharmaceuticals that target specific metabolic pathways.
  • Analytical Uses: It serves as a useful reagent in various analytical techniques, helping chemists understand complex chemical reactions.

As a versatile compound, aminourea also operates as an intermediate in several chemical reactions, showcasing its *practical applications* and *industries of relevance*. Its ability to participate in the formation of more complex organic molecules highlights the interconnectedness of chemistry in both nature and synthetic avenues.

In the words of renowned chemist R. Paul: "The beauty of chemistry lies in its simplicity and complexity, often embodied in compounds like aminourea."

Overall, aminourea stands as a reminder of the *underlying complexities* and *rich potential* within the realm of chemical compounds.

Synonyms
Semicarbazide
HYDRAZINECARBOXAMIDE
57-56-7
Aminourea
Carbamylhydrazine
Carbazamide
Semikarbazid
Aminoharnstoff
Carbamoylhydrazine
Urea, amino-
Carbamidsaeurehydrazid
Aminomocovina
Hydrazine, carbamoyl-
Carbamic acid, hydrazide
EINECS 200-339-6
UNII-37QUC23K2X
BRN 0506319
CHEBI:28306
Semicarbazide, 6 wt% on Silica gel
CHEMBL903
37QUC23K2X
DTXSID7043823
4-03-00-00177 (Beilstein Handbook Reference)
Semikarbazid [Czech]
Aminomocovina [Czech]
isosemicarbazide
amino-urea
1-azanylurea
Urea, amino
Hydrazine, carbamoyl
carbamic acid hydrazide
Lopac-S-2201
Lopac0_001096
DTXCID5023823
BBL012207
BDBM50108606
STL163549
AKOS005716900
Semicarbazide - 6 wt% on Silica gel
CCG-205173
SB86096
SDCCGSBI-0051066.P002
NCGC00015934-01
NCGC00015934-02
NCGC00015934-03
NCGC00015934-04
NCGC00015934-05
NCGC00015934-06
NCGC00091589-02
FS143227
Semicarbazide, 6 wt. % (on silica gel)
NS00100164
C02077
D95915
A831506
Q417535
200-339-6