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p-Nitrosodiphenylamine

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Identification
Molecular formula
C12H10N2O
CAS number
156-10-5
IUPAC name
4-nitroso-N-phenyl-aniline
State
State

Under room temperature conditions, p-Nitrosodiphenylamine is typically found in a solid state, with its distinctive crystalline form.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
198.22g/mol
Molar mass
198.2160g/mol
Density
1.3000g/cm3
Appearence

At room temperature, p-Nitrosodiphenylamine appears as a yellow to green crystalline solid. Its characteristic coloration can aid in its identification in the lab.

Comment on solubility

Solubility of 4-nitroso-N-phenyl-aniline

4-nitroso-N-phenyl-aniline, also known as a specific type of azo compound, showcases particular solubility attributes that can be attributed to its unique chemical structure.

Solubility Characteristics

This compound tends to be:

  • Moderately soluble in organic solvents such as ethanol and acetone.
  • Poorly soluble in water, due to its large aromatic structure which hinders interaction with polar water molecules.
  • Insoluble in non-polar solvents, which may affect its use in various applications.

Factors influencing the solubility of 4-nitroso-N-phenyl-aniline include:

  1. Molecular size and structure: The presence of large phenyl groups limits water solubility.
  2. Intermolecular forces: Hydrogen bonding capabilities play a role in solvation.
  3. Temperature: Increased temperature can enhance solubility in organic solvents.

In summary, understanding the solubility properties of 4-nitroso-N-phenyl-aniline is crucial for its application in chemical processes and formulations. The overall solubility can significantly affect its effectiveness in various chemical environments and formulations.

Interesting facts

Interesting Facts about 4-Nitroso-N-phenyl-aniline

4-Nitroso-N-phenyl-aniline is a fascinating chemical compound that plays a significant role in various fields of chemistry and industry. Here are some intriguing aspects of this compound:

  • Functional Group Diversity: The presence of a nitroso group (-NO) attached to an aniline structure opens up a wide range of chemical reactions that the compound can participate in, such as azo coupling reactions, which are essential in dye chemistry.
  • Applications in Dyes: This compound is often utilized in the dye industry for creating vibrant colors. Its unique structure allows it to form complex dyes that are used in textiles, plastics, and other materials.
  • Biological Implications: Research has shown that compounds similar to 4-nitroso-N-phenyl-aniline can exhibit biological activity, which makes them of interest in pharmacological studies. Understanding the reactivity and potential toxicity of such compounds is crucial for safety assessments.
  • Reaction Mechanisms: As a science enthusiast, studying the reaction mechanisms involving this compound can reveal much about electrophilic substitution reactions, which are foundational in organic chemistry. Exploring how it interacts with various nucleophiles can also be a great exercise in understanding electron transfer processes.
  • Environmental Considerations: Being aware of the environmental impact of chemical compounds like 4-nitroso-N-phenyl-aniline is vital. As a nitroso compound, it can have implications for environmental chemistry, highlighting the importance of responsible handling and disposal in industrial applications.

Overall, 4-nitroso-N-phenyl-aniline is not just a simple organic molecule; it holds a treasure trove of knowledge and applications that illustrate the beauty and complexity of chemical science.

Synonyms
4-NITROSODIPHENYLAMINE
4-Nitroso-N-phenylaniline
156-10-5
p-Nitrosodiphenylamine
Benzenamine, 4-nitroso-N-phenyl-
N-Phenyl-p-nitrosoaniline
p-Nitroso-N-phenylaniline
4-Nitroso-N-phenylbenzenamine
Naugard TKB
Diphenylamine, 4-nitroso-
p-Nitrosodifenylamin
p-Phenylaminonitrosobenzene
NCI-C02244
para-Nitroso-N-phenylaniline
para-Nitrosodiphenylamine
N-Phenyl-para-nitrosoaniline
NSC 5041
p-Nitrosodifenylamin [Czech]
Amine, diphenyl, 4-nitroso-
CCRIS 465
Nitrosodiphenylamine, p-
HSDB 2876
EINECS 205-848-7
BRN 1952651
DTXSID1021031
NSC-5041
N-phenyl-4-nitrosoaniline
TKB
F7052989CV
DTXCID401031
4-Nitroso-N-phenyl-benzenamine
CHEBI:82509
4-12-00-01560 (Beilstein Handbook Reference)
4-NITROSODIPHENYLAMINE [MI]
4-NITROSODIPHENYLAMINE [HSDB]
4-?Nitrosodiphenylamine
P-NITROSODIFENYLAMIN (CZECH)
CAS-156-10-5
UNII-F7052989CV
pNitrosodifenylamin
4nitrosodiphenylamine
MFCD00002062
NPhenylpnitrosoaniline
pNitrosoNphenylaniline
4NitrosoNphenylaniline
Diphenylamine, 4nitroso
NPhenylparanitrosoaniline
paraNitrosoNphenylaniline
pPhenylaminonitrosobenzene
WLN: ONR DMR
4NitrosoNphenylbenzenamine
Amine, diphenyl, 4nitroso
Benzenamine, 4nitrosoNphenyl
SCHEMBL655572
CHEMBL1600998
SCHEMBL11273533
OIJHFHYPXWSVPF-UHFFFAOYSA-
NSC5041
AAA15610
N-(4-Nitrosophenyl)-N-phenylamine
Tox21_201708
Tox21_302822
BBL000066
STK378742
PHENYL 4-NITROSOPHENYL AMINE_
AKOS005448746
N-(4-Nitrosophenyl)-N-phenylamine #
HY-W268942
BENZENAMINE,4-NITROSO-N-PHENYL-
NCGC00091332-01
NCGC00091332-02
NCGC00091332-03
NCGC00091332-04
NCGC00091332-05
NCGC00256585-01
NCGC00259257-01
AS-60940
PD212555
N0263
NS00005589
C19479
D91663
Q27156019
205-848-7
InChI=1/C12H10N2O/c15-14-12-8-6-11(7-9-12)13-10-4-2-1-3-5-10/h1-9,13H