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Diaminomethyleneurea

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Identification
Molecular formula
C3H8N4O
CAS number
35228-25-0
IUPAC name
diaminomethyleneurea
State
State

At room temperature, diaminomethyleneurea is in a solid state, usually as a crystalline powder.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
332.40
Boiling point (Kelvin)
605.50
General information
Molecular weight
101.12g/mol
Molar mass
101.0860g/mol
Density
1.4300g/cm3
Appearence

Diaminomethyleneurea appears as a white to off-white crystalline solid. It is typically available in powder form and may be slightly hygroscopic.

Comment on solubility

Solubility of Diaminomethyleneurea

Diaminomethyleneurea, with the chemical formula C2H8N4O, exhibits notable solubility characteristics that are important for various applications. Understanding its solubility can aid in predicting its behavior in different environments as well as its interaction with other compounds.

Solubility Properties

  • Water Solubility: Diaminomethyleneurea is highly soluble in water, which suggests that it can readily dissolve and engage in reactions in aqueous solutions.
  • Solvent Compatibility: It also demonstrates varying degrees of solubility in other polar solvents, although it is primarily known for its affinity with water.
  • Temperature Effects: Like many compounds, its solubility can be influenced by temperature; typically, increasing temperature enhances solubility.

In summary, the solubility of diaminomethyleneurea is a key feature that can affect its applications in fields such as pharmaceuticals and agriculture. The ability to dissolve easily in water allows it to be effective in systems requiring rapid bioavailability or reaction kinetics, making it a valuable compound in chemical research and development.

Interesting facts

Interesting Facts about Diaminomethyleneurea

Diaminomethyleneurea, commonly referred to as urea, is a fascinating chemical compound with a range of applications in various fields. Here are some notable aspects:

  • Historical Significance: Diaminomethyleneurea was first synthesized in the 18th century, marking a significant milestone in the study of organic chemistry. It was one of the first organic compounds to be artificially produced, which helped shift perspectives on organic substances.
  • Biological Importance: This compound plays a crucial role in the biological process of nitrogen metabolism. In humans and many other organisms, it is a byproduct of protein catabolism, primarily excreted through urine, demonstrating its importance in maintaining nitrogen balance.
  • Industrial Applications: Due to its properties, diaminomethyleneurea is extensively used in agriculture as a fertilizer. It serves as a vital nitrogen source, which is essential for plant growth and development.
  • Pharmaceutical Uses: In the pharmaceutical field, the compound is used as an ingredient in certain medications and formulations, highlighting its versatility and utility.
  • Synthetic Pathways: The synthesis of diaminomethyleneurea is carried out through various methods, including the reaction of ammonia with carbon dioxide, showcasing the innovative approaches taken in organic synthesis.

In the words of a notable chemist, "Understanding compounds like diaminomethyleneurea illustrates the intricate connections within biochemistry and its applications in everyday life." This compound not only enriches our understanding of organic chemistry but also serves practical purposes that impact our world significantly.

Synonyms
Guanylurea
1-Carbamoylguanidine
141-83-3
Dicyandiamidine
1-carbamimidoylurea
Amidinourea
diaminomethylideneurea
N-Carbamoylguanidine
N-Amidinourea
Urea, (aminoiminomethyl)-
Guanidinecarboxamide
Guanidine carboxamide
Urea, amidino-
1-AMIDINOUREA
Urea, guanyl-
(Aminoiminomethyl)urea
Urea, N-(aminoiminomethyl)-
EINECS 205-504-6
UNII-128C2R3P8G
128C2R3P8G
N-(diaminomethylidene)urea
Guanidine, (aminocarbonyl)-
CARBAMOYL-GUANIDINE AMIDINO UREA SALT
DTXSID3043811
Amino([amino(imino)methyl]amino)oxomethane
CARBAMOYLGUANIDINE
Amino((amino(imino)methyl)amino)oxomethane
Dicyandiamidin
SCHEMBL146394
Guanidine carboxylic acid amide
DTXCID1023811
CHEBI:180964
AKOS009031316
FG149798
DB-318892
NS00000584
H27368
Q27251388
9U1