N,N-dimethyl-4-nitrosoaniline
C8H10N2O
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Identification
- CAS Number
- 138-89-6
- EC Number
- 205-343-1
- UN Number
- 1369
- PubChem CID
- 8749
Physical-chemical properties
- Molecular Formula
- C8H10N2O
- Molar Mass
- 150.18 g/mol
- IUPAC Name
- N,N-dimethyl-4-nitrosoaniline
Chemical Identifiers
- InChI
- InChI=1S/C8H10N2O/c1-10(2)8-5-3-7(9-11)4-6-8/h3-6H,1-2H3
- InChI Key
- CMEWLCATCRTSGF-UHFFFAOYSA-N
Overview
N,N-dimethyl-4-nitrosoaniline (CAS 138-89-6) is an aromatic nitroso compound characterized by its distinctive dimethylamino substituent and diagnostic blue-green coloration. This organic chemical compound, with molecular formula C8H10N2O and molecular weight 150.18 g/mol, belongs to the family of nitrosoaniline derivatives that play important roles in analytical chemistry and industrial applications. The compound features a benzene ring substituted with both a dimethylamino group (-N(CH3)2) at the para position and a nitroso group (-NO), creating a conjugated system responsible for its characteristic chromophoric properties. N,N-dimethyl-4-nitrosoaniline exhibits notable chemical reactivity due to the presence of the nitroso functional group, which can participate in various organic transformations including coupling reactions and complexation with metal ions. The compound's stability and reactivity profile differ significantly from related organometallic compounds such as tris(2-methylpropyl)alumane, highlighting the diverse chemical behavior within different compound classes. Under normal storage conditions, the material requires careful handling to prevent decomposition, particularly when exposed to light or elevated temperatures. The compound finds primary application as an analytical reagent for metal detection and quantification, particularly in spectrophotometric analysis methods. It serves as an important intermediate in organic synthesis, enabling the preparation of various dye compounds and pharmaceutical intermediates. Additionally, N,N-dimethyl-4-nitrosoaniline is utilized in research applications for studying nitroso group chemistry and developing new analytical methodologies. As a specialized distributor of technical chemicals across Europe, OYSI maintains reliable supply chains for N,N-dimethyl-4-nitrosoaniline to support analytical laboratories and chemical manufacturing operations requiring this specific nitrosoaniline derivative.
Safety & Classification
No Hazard Classification
This substance is not classified as hazardous according to CLP Regulation (EC) No 1272/2008.
Transport (ADR)
| UN Number | 1369 |
| ADR Class | 4.2 |
| Packing Group | II |
| Tunnel Code | D/E |
| Proper Shipping Name | p-Nitrosodimethylanilin |
| Marine Pollutant | No |
Frequently Asked Questions
What is N,N-dimethyl-4-nitrosoaniline?
N,N-dimethyl-4-nitrosoaniline is an organic chemical compound with the molecular formula C8H10N2O and CAS number 138-89-6. This aromatic amine derivative has a molecular weight of 150.18 g/mol and belongs to the nitroso compound family. It features a dimethylamino group attached to an aniline ring with a nitroso functional group, making it valuable in various chemical synthesis applications and analytical procedures.
What are the physicochemical properties of N,N-dimethyl-4-nitrosoaniline?
N,N-dimethyl-4-nitrosoaniline is typically a solid crystalline compound at room temperature with a characteristic green to dark green color. The compound exhibits moderate solubility in organic solvents such as ethanol and acetone, while showing limited water solubility. It has a molecular weight of 150.18 g/mol and contains both electron-donating dimethylamino and electron-withdrawing nitroso groups, which influence its reactivity and spectroscopic properties.
What is N,N-dimethyl-4-nitrosoaniline used for?
N,N-dimethyl-4-nitrosoaniline is primarily used as a chemical intermediate in organic synthesis and as an analytical reagent. It serves as a precursor for dye manufacturing, particularly in the production of certain colored compounds. The substance is also employed in research laboratories for spectroscopic studies and chemical analysis due to its unique chromophoric properties. Additionally, it finds applications in pharmaceutical intermediate synthesis and specialty chemical production.
How to handle N,N-dimethyl-4-nitrosoaniline safely?
N,N-dimethyl-4-nitrosoaniline should be handled with standard laboratory safety precautions including wearing appropriate personal protective equipment such as safety goggles, lab coat, and chemical-resistant gloves. Work should be conducted in a well-ventilated area or under a fume hood to avoid inhalation. Avoid direct skin contact and ingestion. Use proper handling techniques to prevent dust formation and ensure all equipment is grounded when handling this substance.
How to store N,N-dimethyl-4-nitrosoaniline correctly?
N,N-dimethyl-4-nitrosoaniline should be stored in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Keep the container tightly closed when not in use to prevent moisture absorption and contamination. Store separately from strong oxidizing agents, acids, and bases. The storage area should be equipped with appropriate fire suppression systems and the containers should be properly labeled with hazard information.
What to do in case of contact with N,N-dimethyl-4-nitrosoaniline?
In case of skin contact with N,N-dimethyl-4-nitrosoaniline, immediately wash the affected area with plenty of water and soap for at least 15 minutes. If eye contact occurs, flush eyes with clean water for 15 minutes and seek medical attention. In case of inhalation, move to fresh air immediately. If ingested, rinse mouth with water and seek immediate medical attention. Do not induce vomiting and contact emergency services if symptoms persist.
How to dispose of N,N-dimethyl-4-nitrosoaniline properly?
N,N-dimethyl-4-nitrosoaniline must be disposed of in accordance with local, national, and international waste regulations. The substance should not be discharged into drains, soil, or water bodies. Contact licensed waste disposal companies for proper treatment and disposal. Small quantities can be treated through approved chemical waste programs, while larger amounts require specialized hazardous waste handling. Always consult local environmental authorities for specific disposal requirements.
How to transport N,N-dimethyl-4-nitrosoaniline?
N,N-dimethyl-4-nitrosoaniline is classified under ADR Class 4.2 (substances liable to spontaneous combustion) with Packing Group II. Transportation requires appropriate UN specification packaging and proper labeling according to dangerous goods regulations. Vehicles must carry appropriate fire suppression equipment and drivers need dangerous goods training. Shipping documents must include proper shipping names, hazard class, and emergency response information. Consult current ADR regulations for complete transport requirements.
Is N,N-dimethyl-4-nitrosoaniline subject to specific regulations?
N,N-dimethyl-4-nitrosoaniline is subject to standard chemical regulations including REACH registration requirements in Europe and CLP classification obligations. While not currently listed as a Substance of Very High Concern (SVHC), it must comply with general chemical safety regulations, workplace exposure limits, and environmental protection measures. Users must maintain safety data sheets and implement appropriate risk management measures according to local and regional chemical legislation.
Where to buy N,N-dimethyl-4-nitrosoaniline in Europe?
N,N-dimethyl-4-nitrosoaniline is available through OYSI, a leading European distributor of specialty chemicals and industrial compounds. OYSI provides high-quality chemical products to laboratories, research institutions, and industrial customers across Europe. For availability, specifications, and ordering information, contact OYSI directly through their website or sales representatives. They can provide detailed product information, safety documentation, and technical support for your specific application requirements.
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Data Sources
Classification per CLP Regulation (EC) No 1272/2008. Data from ECHA and PubChem.