Basic information
- CAS
120-22-9- Standard SMILES
CCN(CC)c1ccc(N=O)cc1- InChIKey
OLNMJIHADFYHAK-UHFFFAOYSA-N- Molecular formula
- C10H14N2O
- Average molar mass
- 178.23 g/mol
- Monoisotopic mass
- 178.11061307
Overview
P-nitrosodiethylaniline is a green solid. Insoluble in water.
Names & identifiers
- Preferred name
- N,N-diethyl-4-nitrosoaniline
- IUPAC
- N,N-diethyl-4-nitrosoaniline
- English name
- N,N-Diethyl-4-nitrosoaniline
- Molecular formula
- C10H14N2O
- Molecular weight
- 178.23
Names & synonyms
N,N-Diethyl-4-nitrosoaniline120-22-94-Nitroso-N,N-diethylanilinep-NitrosodiethylanilineN,N-Diethyl-p-nitrosoanilineN,N-Diethyl-4-nitrosobenzenamineBenzenamine, N,N-diethyl-4-nitroso-p-Nitroso-N,N-diethylanilineAniline, N,N-diethyl-p-nitroso-5QX2AS44RVPara-nitroso-N,N-diethylanilineNSC-5418
Show more names
Diethyl-p-nitrosoanilineDIETHYL-4-NITROSO-ANILINEn,n-diethyl-p-nitroso-anilin
DTXSID3059507RefChem:161167DTXCID1033531204-379-5Diethylnitrosoaniline4-DiethylaminonitrosobenzeneNSC 5418MFCD00002064
Database identifiers
- CAS
120-22-9- PubChem CID
- 67115
- DTXSID
DTXSID3059507- UNII
- 5QX2AS44RV
- EC Number
- 204-379-5
- Nikkaji
- J29.618J
Properties
Computed structural properties
- XLogP
- 2.1
- Topological polar surface area
- 32.7 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 3
- Heavy atoms
- 13
- Formal charge
- 0
- Complexity
- 149
Experimental & physicochemical properties
SpringerMaterials PropertiesDiamagnetic susceptibility
Physical DescriptionP-nitrosodiethylaniline is a green solid. Insoluble in water.
Physicochemical properties
- Melting point
- 81 · 81-85 °C
- Boiling point
- 310.47 °C · 310.47°C (rough estimate)
- Density
- 1.24 · 1.2400
- refractive index
- 1.525 · 1.5250 (estimate)
- storage temp.
- Flammables area
- Water Solubility
- Slightly soluble in water
- form
- powder to crystal
- pka
- 0.67 · 0.67±0.32(Predicted)
- color
- Green to Dark green
- CAS DataBase Reference
- 120 · 120-22-9(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
Safety & regulation
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
GHS classification
GHS Classification
This chemical does not meet GHS hazard criteria for 2.3% (1 of 44) of reports.
Danger
H228 (11.4%): Flammable solid [Danger Flammable solids]
P210, P240, P241, P261, P262, P264, P270, P271, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 44 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
DOT LabelFlammable Solid Poison
Fire HazardsExcerpt from ERG Guide 134 [Flammable Solids - Toxic and/or Corrosive]:
Health HazardsExcerpt from ERG Guide 134 [Flammable Solids - Toxic and/or Corrosive]:
Reactive GroupNitro, Nitroso, Nitrate, and Nitrite Compounds, Organic
Reactivity Profile
A nitrated aromatic 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.
Chemistry & industry
Uses & manufacturing
General Manufacturing InformationBenzenamine, N,N-diethyl-4-nitroso-: ACTIVE
Applications
UsesN,N-Diethyl-4-nitrosobenzenamine reacts with rubber to form a compound that acts as efficient antioxidants.
General DescriptionGreen solid. Insoluble in water.
Upstream & downstream products
Upstream raw materials
Downstream products
Related reactions
3 records
Compound notes
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