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Diazald

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Identification
Molecular formula
C6H10N2O2
CAS number
80-11-5
IUPAC name
N,N-diallylnitrous amide
State
State

At room temperature, Diazald is usually found in a solid form. It is most commonly used in laboratories due to its utility in generating diazomethane.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.15
Boiling point (Celsius)
224.00
Boiling point (Kelvin)
497.15
General information
Molecular weight
144.18g/mol
Molar mass
144.1810g/mol
Density
1.0600g/cm3
Appearence

Diazald is typically a white or off-white crystalline solid. It may also appear as a powder and is often found in laboratory settings where it's used for diazomethane generation. The solid form of the compound tends to cake under certain conditions.

Comment on solubility

Solubility of N,N-diallylnitrous amide

The solubility of N,N-diallylnitrous amide in various solvents can provide important insights into its chemical behavior and potential applications. This compound typically exhibits partial solubility in organic solvents, which is influenced by several factors, including:

  • Polarity: Being an organic compound, N,N-diallylnitrous amide is more likely to dissolve in polar organic solvents but may have limited solubility in non-polar solvents.
  • Temperature: Increased temperature generally enhances solubility, allowing greater interactions between the solute and solvent molecules.
  • Concentration: Higher concentrations can affect the solubility limit and lead to saturation, impacting further solute behavior.

It is noted that compounds like N,N-diallylnitrous amide may also interact with water, although their solubility in aqueous solutions can be limited. In the context of mixtures, the presence of other solutes can influence the overall solubility due to competitive interactions.

To summarize:

  1. N,N-diallylnitrous amide is moderately soluble in certain organic solvents.
  2. Temperature and solvent type play crucial roles in its solubility.
  3. Interactions with other components can further affect solubility dynamics.

Understanding the solubility profile of N,N-diallylnitrous amide is essential for its practical application in chemical processes and formulations.

Interesting facts

N,N-Diallylnitrous Amide: Fascinating Insights

N,N-Diallylnitrous amide is an intriguing compound that has caught the attention of both chemists and industrial researchers due to its unique structure and potential applications. Here are some compelling facts about this compound:

  • Versatile Reactivity: N,N-diallylnitrous amide is known for its ability to participate in various chemical reactions, making it a valuable intermediate in organic synthesis.
  • Inhibition of Biological Processes: Research indicates that this compound has potential as a biocidal agent, with applications in agricultural chemistry where it can help control harmful microorganisms.
  • Role in Hypoxia Research: The nitrous amide functional group present in its structure has sparked interest in studies related to hypoxia, which is the deficiency of oxygen in tissues.
  • Chemical Stability: Its stability under various conditions allows for easy manipulation in laboratory settings, which is crucial for developing new substances or exploring its reactivity further.
  • Educational Relevance: This compound serves as an excellent example in academic settings for studying amides and exploring the principles of organic chemistry and reaction mechanisms.

As chemists delve deeper into the properties and applications of N,N-diallylnitrous amide, they find it is not merely a compound of interest but a gateway to exploring the vast field of organic reactions and their practical utilities.

Synonyms
Diallylnitrosamine
16338-97-9
Diallylamine, N-nitroso-
Diallylnitrosamin
2-Propen-1-amine, N-nitroso-N-2-propenyl-
N-nitroso-N-diallylamine
NSC-37648
QZ22XCT9RV
DTXSID2020395
N-Nitroso-N-2-propen-1-yl-2-propen-1-amine
NDAA
DTXCID60395
N-Nitrosodiallylamine
N,N-bis(prop-2-enyl)nitrous amide
N-Diallylnitrosamine
N-Nitroso-N,N-diallylamine
N-Diallynitrosamine
Nitrosodiallyamine
N-Nitrosodiallyl amine
Diallylnitrosamin [German]
CCRIS 6153
N,N-diallylnitrous amide
NSC 37648
BRN 1922991
nitrosodiallylamine
Nitrosodiallylamine, N-
N,N-DI(PROP-2-ENYL)NITROUS AMIDE
N-nitroso-N-prop-2-en-1-ylprop-2-en-1-amine
1,1-diallyl-2-oxohydrazine
WLN: 1U2NNO&2U1
CHEMBL164131
SCHEMBL3210308
GRYFJBRXMFVEIL-UHFFFAOYSA-N
NSC37648
AKOS006277388
Q63088177