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1,3-Dianilinourea

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Identification
Molecular formula
C13H14N4O
CAS number
6219-71-2
IUPAC name
1,3-dianilinourea
State
State

At room temperature, 1,3-Dianilinourea is in a solid state, typically found as a crystalline powder.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.15
Boiling point (Celsius)
333.80
Boiling point (Kelvin)
606.95
General information
Molecular weight
242.27g/mol
Molar mass
242.2690g/mol
Density
1.3500g/cm3
Appearence

1,3-Dianilinourea typically appears as an off-white to pale yellow crystalline solid. It may be presented in a powdered form with a slightly granular texture.

Comment on solubility

Solubility of 1,3-Dianilinourea

When it comes to the solubility of 1,3-dianilinourea, several factors play a crucial role. This compound exhibits a unique solubility profile influenced by its molecular structure and the presence of functional groups. Here's what you need to know:

  • Polarity: The presence of amino groups (-NH2) in its structure contributes to its varying solubility in different solvents, giving the molecule a degree of polarity.
  • Solvent Interaction: 1,3-dianilinourea tends to dissolve well in polar solvents like water and alcohols, while showing limited solubility in non-polar solvents.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature—higher temperatures often result in greater solubility levels.
  • pH Dependency: The solubility can also be affected by the pH of the solution, as the protonation state of the amino groups may change.

In summary, while 1,3-dianilinourea demonstrates good solubility in polar environments, it is essential to consider solvent type, temperature, and solution pH to fully understand its solubility characteristics.

Interesting facts

Interesting Facts about 1,3-Dianilinourea

1,3-Dianilinourea is an intriguing compound that boasts several fascinating attributes. As a derivative of urea, it plays a role in various chemical reactions and has applications in multiple fields, including pharmaceuticals and agriculture.

Key Characteristics:

  • Structural Significance: The compound features two aniline groups attached to a central urea moiety, which contributes to its unique properties.
  • Biological Activity: Compounds containing aniline groups often exhibit interesting biological activities, making them valuable in drug development.
  • Intermolecular Interactions: Due to the presence of hydrogen bonds within its structure, 1,3-dianilinourea can engage in significant intermolecular interactions, impacting its behavior in various environments.

Applications:

  • It has potential uses in the field of medicinal chemistry, particularly in the design of molecules for treating various diseases.
  • In agricultural applications, compounds like this may serve as herbicides or fertilizers to enhance crop yield and resistance.
  • Ongoing research explores its utility in constructing polymers or as a precursor in organic synthesis.

As noted by chemists, "Understanding the subtle variations in molecular structure can lead to breakthroughs in material science and pharmaceuticals." This quote effectively encapsulates the essence of why compounds like 1,3-dianilinourea are so vital in ongoing scientific progress.

In summary, 1,3-dianilinourea, with its unique composition and promising applications, offers a broad range of possibilities for future research and development in both chemistry and related fields.

Synonyms
1,5-Diphenylcarbazide
140-22-7
Diphenylcarbazide
1,5-Diphenylcarbohydrazide
Carbonic dihydrazide, 2,2'-diphenyl-
1,5-Diphenylcarbonohydrazide
1,3-dianilinourea
SYM-DIPHENYLCARBAZIDE
N,N'-Diphenylcarbazide
2,2'-Diphenylcarbazide
1,5-Diphenylcabohydrazide
2,2'-Diphenylcarbonic dihydrazide
2,5-Diphenylcarbazide
Carbohydrazide, 1,5-diphenyl-
AI3-00869
UNII-1W1XPA8N0P
1,5-Diphenylcarbohydrazine
NSC 5058
EINECS 205-403-7
MFCD00003013
s-Diphenyl carbazide
BRN 0752039
1,5 diphenylcarbazide
N'',N'''-Diphenylcarbonohydrazide
NSC-5058
1W1XPA8N0P
DTXSID7059690
SYM-DIPHENYLCARBAZIDE [MI]
4-15-00-00182 (Beilstein Handbook Reference)
Diphenyl carbazide
diphenylcarbazid
s-diphenylcarbazide
S Diphenylcarbazide
2,5Diphenylcarbazide
N,N'Diphenylcarbazide
2,2'Diphenylcarbazide
1,5Diphenylcabohydrazide
1,5Diphenylcarbohydrazide
1,5-Diphenylcarbohydrazid
1,3-bis(phenylamino)urea
Carbohydrazide,5-diphenyl-
1,5Diphenylcarbonohydrazide
Carbohydrazide, 1,5diphenyl
CBDivE_014231
SCHEMBL294587
CHEBI:4641
DTXCID8034536
SCHEMBL26622644
2,2'Diphenylcarbonic dihydrazide
NSC5058
Carbonic dihydrazide,2'-diphenyl-
HMS1578M04
1,5-Diphenylcarbazide, ACS grade
Carbonic dihydrazide, 2,2'diphenyl
N',N''-Diphenylcarbonohydrazide #
1,5-Diphenylcarbazide, ACS reagent
STL283945
1,5-Diphenylcarbazide, reagent grade
AKOS000120184
CS-W012774
FD00529
1,5-Diphenylcarbazide, JIS special grade
AS-13073
SY010365
D1513
NS00024543
EN300-19423
SR-01000196298
Q1227137
SR-01000196298-1
1,5-Diphenylcarbazide, p.a., ACS reagent, reag. Ph. Eur.
1,5-Diphenylcarbazide, Reag. Ph. Eur., >=98.0%, for metal titration
205-403-7