N,N-Diethyl-4-nitrosoaniline

N,N-Diethyl-4-nitrosoaniline Basic information
Product Name:N,N-Diethyl-4-nitrosoaniline
Synonyms:p-Nitroso-N,N-diethylaniline;n,n-diethyl-p-nitroso-anilin;N,N-DIETHYL-P-NITROSOANILINE;N,N-DIETHYL-4-NITROSOANILINE;P-NITROSODIETHYLANILINE;N N-DIETHYL-4-NITROSOANILINE 97%;N,N-Diethyl-4-nitrosoaniline,98%;N,N-Diethyl-4-nitrosoaniline
CAS:120-22-9
MF:C10H14N2O
MW:178.23
EINECS:204-379-5
Product Categories:
Mol File:120-22-9.mol
N,N-Diethyl-4-nitrosoaniline Structure
N,N-Diethyl-4-nitrosoaniline Chemical Properties
Melting point 81-85 °C
Boiling point 310.47°C (rough estimate)
density 1.2400
refractive index 1.5250 (estimate)
storage temp. Flammables area
pka0.67±0.32(Predicted)
CAS DataBase Reference120-22-9(CAS DataBase Reference)
EPA Substance Registry SystemBenzenamine, N,N-diethyl-4-nitroso- (120-22-9)
Safety Information
Hazard Codes T-F,T
Risk Statements 33-23/24/25-11
Safety Statements 45-36/37/39-22-16
RIDADR 2926
RTECS BX3610000
HazardClass 4.1
PackingGroup II
Toxicitymmo-sat 3 mmol/L XENOBH 16,587,86
MSDS Information
ProviderLanguage
ACROS English
ALFA English
N,N-Diethyl-4-nitrosoaniline Usage And Synthesis
Chemical Propertiesgreen crystalline powder
UsesN,N-Diethyl-4-nitrosobenzenamine reacts with rubber to form a compound that acts as efficient antioxidants.
General DescriptionGreen solid. Insoluble in water.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileA nitrated amine. Amines are combustible. The combustion of amines yields noxious NOx. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.
Safety ProfileMutation data reported. When heated to decomposition it emits toxic vapors of NOx.
Tag:N,N-Diethyl-4-nitrosoaniline(120-22-9) Related Product Information
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