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N,N-Dimethyl-4-nitrosoaniline

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Identification
Molecular formula
C8H10N2O
CAS number
138-89-6
IUPAC name
N,N-dimethyl-4-nitroso-aniline
State
State
At room temperature, N,N-Dimethyl-4-nitrosoaniline is in a solid state, presenting itself as yellow to orange crystals.
Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
334.00
Boiling point (Kelvin)
607.15
General information
Molecular weight
150.18g/mol
Molar mass
150.1770g/mol
Density
1.2045g/cm3
Appearence

N,N-Dimethyl-4-nitrosoaniline usually appears as a yellow to orange crystalline solid. It is known for its distinct coloration, which can give a visual clue to its presence in chemical mixtures or reactions.

Comment on solubility

Solubility of N,N-dimethyl-4-nitroso-aniline

N,N-dimethyl-4-nitroso-aniline, a compound with the formula C8H10N2O, exhibits varying solubility characteristics that can be influenced by multiple factors. Understanding its solubility profile is crucial in both laboratory applications and industrial processes. Here are some points to consider:

  • Polarity: The presence of the nitroso group contributes to the compound's overall polarity, which can enhance its solubility in polar solvents, such as water.
  • Solvent Compatibility: N,N-dimethyl-4-nitroso-aniline may be more soluble in organic solvents like ethanol and acetone compared to nonpolar solvents due to its functional groups.
  • Temperature Influence: Increasing temperature often improves solubility, allowing for higher concentrations of the compound to dissolve in a solution.
  • Concentration Limits: Care should be taken to assess the solubility limit, as saturation can lead to precipitation, especially in polar solvents.

In conclusion, while N,N-dimethyl-4-nitroso-aniline shows favorable solubility in certain solvents, it is important to conduct specific solubility tests under controlled conditions to determine the most suitable solvent for your specific applications. Remember, “solubility is not merely an attribute, but a gateway to chemical interactions.”

Interesting facts

Interesting Facts about N,N-Dimethyl-4-nitroso-aniline

N,N-Dimethyl-4-nitroso-aniline is a compound that showcases both fascinating chemistry and various applications in industrial fields. Here are some interesting aspects of this compound:

  • Classification: This compound belongs to the class of nitrosoanilines, which are known for their ability to participate in various chemical reactions due to the presence of both amino and nitroso functional groups.
  • Use in Dyes: One of the primary applications of N,N-dimethyl-4-nitroso-aniline is its role in the synthesis of azo dyes, which are widely used in textiles, food coloring, and even cosmetics.
  • Reaction Mechanism: The compound can undergo reduction reactions, which lead to the formation of various derivatives. Understanding these reactions can help chemists design new compounds with desired properties.
  • Health Considerations: Like many nitrogen-containing compounds, N,N-dimethyl-4-nitroso-aniline requires careful handling due to potential health risks associated with nitrosamines, which can be carcinogenic.
  • Research Significance: The study of N,N-dimethyl-4-nitroso-aniline can provide insights into the reactivity of nitroso compounds, contributing to broader fields like medicinal chemistry and materials science.

As with many compounds, knowledge is power, and understanding the chemistry underlying N,N-dimethyl-4-nitroso-aniline not only aids in its safe handling but also opens doors to new innovations in various fields. Its versatility makes it a compound of interest for chemists and industry professionals alike!

Synonyms
N,N-Dimethyl-4-nitrosoaniline
138-89-6
Accelerine
p-Nitroso-N,N-dimethylaniline
4-Nitrosodimethylaniline
Benzenamine, N,N-dimethyl-4-nitroso-
4-Nitroso-N,N-dimethylaniline
N,N-DIMETHYL-P-NITROSOANILINE
p-(Dimethylamino)nitrosobenzene
p-Nitrosodimethylanilide
Paranitrosodimethylanilide
p-Nitrosodimethylaniline
Dimethyl(p-nitrosophenyl)amine
4-(Dimethylamino)nitrosobenzene
Ultra Brilliant Blue P
p-(N,N-Dimethylamino)nitrosobenzene
N,N-Dimethyl-4-nitrosobenzenamine
NCI-C01821
Aniline, N,N-dimethyl-p-nitroso-
Dimethyl-p-nitrosoaniline
p-Nitroso dimethylaniline
NSC 2775
Accelerene
CCRIS 3057
N,N-dimethyl-4-nitroso-aniline
HSDB 1320
EINECS 205-343-1
UN1369
BRN 0607293
726V2ETM9E
DTXSID7025138
CHEBI:59990
AI3-15393
NSC-2775
MFCD00002063
DTXCID805138
N,N'-dimethyl-4-nitrosoaniline
NSC2775
4-12-00-01558 (Beilstein Handbook Reference)
DIMETHYL-P-NITROSOANILINE, N,N-
P-NITROSO-N,N-DIMETHYLANILINE [MI]
N,N-DIMETHYL-P-NITROSOANILINE [HSDB]
CAS-138-89-6
para-nitrosodimethylaniline
Benzen-2,6-d2-amine, N,N-dimethyl-4-nitroso-
NDMA nitrosodimethylaniline
UNII-726V2ETM9E
Vulcaniline
1-(Dimethylamino)-4-nitrosobenzene
p-nitrosodimethylanilin
pNitrosodimethylanilide
pNitrosodimethylaniline
13139-88-3
4Nitrosodimethylaniline
NDMA (Substrate 4)
P-NDMA
pNitrosoN,Ndimethylaniline
4NitrosoN,Ndimethylaniline
N,NDimethyl4nitrosoaniline
Aniline, 4-nitrosodimethyl
Aniline, N,Ndimethylpnitroso
Dimethyl(pnitrosophenyl)amine
p(Dimethylamino)nitrosobenzene
4(Dimethylamino)nitrosobenzene
N,NDimethyl4nitrosobenzenamine
SCHEMBL103850
Aniline,N-dimethyl-p-nitroso-
CHEMBL1569493
n,n-dimethyl-para-nitrosoaniline
WLN: ONR DN1 & 1
Benzenamine, N,Ndimethyl4nitroso
p(N,NDimethylamino)nitrosobenzene
BDBM108227
Benzenamine,N-dimethyl-4-nitroso-
dimethyl-(4-nitroso-phenyl)-amine
aniline, N,N-dimethyl-4-nitroso-
Tox21_202129
Tox21_303049
STL264252
AKOS005208791
N,N-Dimethyl-4-nitrosoaniline, 97%
N,N-DIMETHYL-P-NITROSO ANILINE
N,N-dimethyl-N-(4-nitrosophenyl)amine
PS-4800
UN 1369
NITROSOANILINE, N,N-DIMETHYL-P-
NCGC00091697-01
NCGC00091697-02
NCGC00091697-03
NCGC00091697-04
NCGC00091697-05
NCGC00257004-01
NCGC00259678-01
4-NITROSO-N,N-DIMETHYLAMINOBENZENE
DB-361230
N0262
NS00024493
A50923
C19680
A807455
AB-131/40181212
Q26840963
p-Nitrosodimethylaniline [UN1369] [Spontaneously combustible]
205-343-1