Nitrosodiphenylamine | Solubility of Things

Identification

Molecular formula

C₁₂H₁₀N₂O

CAS number

156-10-5

IUPAC name

N,N-diphenylnitrous amide

State

At room temperature, nitrosodiphenylamine is generally found in a solid state. This state remains consistent under standard conditions of temperature and pressure.

Melting point (Celsius)

67.00

Melting point (Kelvin)

340.15

Boiling point (Celsius)

164.50

Boiling point (Kelvin)

437.65

General information

Molecular weight

198.22g/mol

Molar mass

198.2280g/mol

Density

1.2300g/cm³

Appearence

Nitrosodiphenylamine typically appears as a yellow to brown solid. The compound may present itself in powder form, depending on the conditions of its storage and any processing it may have undergone. Its appearance can vary slightly depending on impurities it may contain and its storage condition.

Comment on solubility

Solubility of N,N-diphenylnitrous amide

N,N-diphenylnitrous amide, a compound with the chemical formula C₁₂H₁₂N₂O, presents interesting solubility characteristics that are influenced by its unique molecular structure. Generally, the solubility of organic compounds can be analyzed based on various factors such as polarity, hydrogen bonding capacity, and molecular interactions. In the case of N,N-diphenylnitrous amide, the following points are particularly noteworthy:

Polarity: The presence of the nitrous amide functional group lends some polarity to the molecule; however, the overall structure remains relatively hydrophobic due to the bulky phenyl groups.
Solvent Interaction: N,N-diphenylnitrous amide is expected to be more soluble in organic solvents such as ethanol, acetone, and chloroform rather than in polar solvents like water.
Hydrogen Bonding: While it can form hydrogen bonds, the steric hindrance created by the phenyl groups may limit its interaction with solvent molecules.

As a result, N,N-diphenylnitrous amide exhibits limited solubility in aqueous solutions, which is a common trait among many organic compounds with substantial hydrophobic components. This characteristic can influence its applications and behavior in various chemical processes.

Interesting facts

Exploring N,N-Diphenylnitrous Amide

N,N-Diphenylnitrous amide is a fascinating compound that has captured the interest of chemists and researchers alike due to its unique structural properties and potential applications. Here are some engaging facts about this intriguing compound:

Structural Characteristics: N,N-diphenylnitrous amide is distinguished by the presence of two phenyl groups attached to a nitrous amide functional group. This creates a compound with a planar structure, leading to interesting interactions at the molecular level.
Chemical Reactivity: The nitrous amide moiety can undergo various chemical transformations. It is known to be susceptible to hydrolysis and can participate in reactions that are significant in synthetic organic chemistry.
Applications in Synthesis: The compound serves as a useful intermediate in organic synthesis. Its functionality allows chemists to build more complex structures, which can lead to the development of pharmaceuticals or agrochemicals.
Research Significance: N,N-Diphenylnitrous amide has been the subject of investigations related to its reactivity patterns, leading to insights into *nitrous compounds* in general. The study of such compounds often unveils their behavior under varying conditions, beneficial for developing new reactions.
Comparative Chemistry: Similar compounds, such as other nitrous amides, display different properties and reactivity, allowing for comparative studies. Researchers often explore these compounds to understand the influence of structural variations on chemical behavior.

In conclusion, N,N-diphenylnitrous amide embodies a blend of chemical intrigue and practical applicability. The compound's significance extends beyond its structure, making it a valuable subject of study for both students and professionals in the field of chemistry.

Synonyms

N-NITROSODIPHENYLAMINE

86-30-6

Diphenylnitrosamine

Nitrosodiphenylamine

Benzenamine, N-nitroso-N-phenyl-

Vultrol

N-Nitroso-N-phenylaniline

Retarder J

Redax

Vulcatard A

Vulkalent A

Ortard

Sconoc

Vulcalent A

Curetard A

Diphenylnitrosamin

Diphenylamine, N-nitroso-

Naugard TJB

Delac J

N,N-Diphenylnitrosamine

N-Nitrosodifenylamin

Vulcatard

N-NITROSO-DIPHENYLAMINE

Difenylnitrosamin

NdphA

Diphenyl N-nitrosoamine

Vulkalent A [Czech]

NCI-C02880

N-Nitroso-N-phenylbenzenamine

Difenylnitrosamin [Czech]

N,N-diphenylnitrous amide

NSC 585

Diphenylnitrosamin [German]

N-Nitrosodifenylamin [Czech]

CCRIS 464

HSDB 2875

UNII-AP2V89J1DA

EINECS 201-663-0

AP2V89J1DA

BRN 0909531

DTXSID6021030

AI3-00698

NSC-585

N-Nitroso-N-diphenylamine

N,N-Diphenyl-N-nitrosoamine

DTXCID001030

CHEBI:34875

N-NITROSODIPHENYLAMINE [HSDB]

N-NITROSODIPHENYLAMINE [IARC]

TJB

VULKALENT A (CZECH)

DIPHENYLNITROSAMIN (GERMAN)

N-NITROSODIFENYLAMIN (CZECH)

N-NITROSODIPHENYLAMINE (IARC)

CAS-86-30-6

NNitrosodifenylamin

Diphenylnitrosoamine

diphenyl nitrosamine

NNitrosodiphenylamine

NNitrosoNphenylaniline

Diphenyl Nnitrosoamine

N,NDiphenylnitrosamine

Diphenylamine, Nnitroso

NNitrosoNphenylbenzenamine

WLN: ONNR&R

PHENYL-N-NITROSOAMINE

SCHEMBL80329

BIDD:ER0645

N,N'-diphenylnitrous hydrazide

N-Nitroso-N-phenyl benzenamine

CHEMBL165491

NSC585

2-Oxo-1,1-diphenylhydrazine #

TDA95195

Tox21_201457

Tox21_300574

MSK4916-100M

STL453728

AKOS015915016

MSK4916-1000M

NCGC00091777-01

NCGC00091777-02

NCGC00091777-03

NCGC00091777-04

NCGC00254349-01

NCGC00259008-01

BS-43792

N-Nitrosodiphenylamine, analytical standard

D0899

NS00000623

E78934

EN300-7476948

N-Nitrosodiphenylamine, technical, >=97.0% (N)

Q4995308

N-NITROSODIPHENYLAMINE (2,2',4,4',6,6'-D6)

N-Nitrosodiphenylamine Solution in Methanol, 100_g/mL

N-Nitrosodiphenylamine Solution in Methanol, 1000_g/mL

Z276119944