Substance

ID:719218

N,N-Dimethyl-4-nitrosoaniline

Names and Identifiers
IUPAC Traditional name
NDMA
IUPAC name
N,N-dimethyl-4-nitrosoaniline
Synonyms
4-Nitroso-N,N-dimethylanilineN,N-Dimethyl-4-nitrosoanilineN,N-二甲基-4-亚硝基苯胺
Registration numbers
Beilstein Number
MDL Number
EC Number
CAS Number
Merck Index
Properties
Physical Property
Density
1.150
Melting Point
84-87°C
Safety Information
GHS Pictograms
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS06
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS Hazard statements
H228-H251-H301-H310-H351-H373
European Hazard Symbols
Flammable Flammable (F)
Toxic Toxic (T)
RTECS
BX7175000
Safety Statements
16-20-27-36/37-45
Risk Statements
11-24/25-33-40
TSCA Listed
GHS Precautionary statements
P210-P241-P301+P310-P361-P405-P501A
Hazard Class
4.2
UN Number
UN1369
Packing Group
II
Product Information
Purity
98%
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Reagent for the conversion of toluenes with activated methyl groups to aldehydes, by condensation and subsequent hydrolysis of the imine: Org. Synth. Coll., 2, 223 (1943):
• Similarly, converts benzylpyridinium salts to aldehydes (Krohnke reaction): Org. Synth. Coll., 5, 825 (1973).