7346-14-7

Basic information

• Product Name: NNDINITROSONNDIETHYLETHYLENEDIAMINE
• Synonyms: NNDINITROSONNDIETHYLETHYLENEDIAMINE;NSC-62579
• CAS NO: 7346-14-7
• Molecular Formula: C₆H₁₄N₄O₂
• Molecular Weight: 174.20096
• Mol File: 7346-14-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 305.18°C (rough estimate)
• Appearance: /
• Density: 1.2297 (rough estimate)
• Refractive Index: 1.6700 (estimate)
• CAS DataBase Reference: NNDINITROSONNDIETHYLETHYLENEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: NNDINITROSONNDIETHYLETHYLENEDIAMINE(7346-14-7)
• EPA Substance Registry System: NNDINITROSONNDIETHYLETHYLENEDIAMINE(7346-14-7)

Safety Data

• Hazardous Substances Data: 7346-14-7(Hazardous Substances Data)

Usage

General Description

NNDINITROSONNDIETHYLETHYLENEDIAMINE is a chemical compound with the molecular formula C4H12N4O2. It is a highly reactive and toxic compound that is used in the production of rubber and plastics. It is a known carcinogen and can cause serious health effects if ingested, inhaled, or absorbed through the skin. Exposure to NNDINITROSONNDIETHYLETHYLENEDIAMINE can lead to respiratory issues, skin irritation, and damage to the liver and kidneys. It is important to handle and store this chemical with extreme caution and to minimize exposure to it in order to prevent harm to human health and the environment.

Relevant articles and documents

Nitric oxide reactivity of copper(ii) complexes of bidentate amine ligands: Effect of substitution on ligand nitrosation

Three copper(ii) complexes with bidentate ligands L1, L 2 and L3 [L1, N,N/- dimethylethylenediamine; L2, N,N/-diethylethylenediamine and L3, N,N/-diisobutylethylenediamine], respectively, were synthesized as their perchlorate salts. The single crystal structures for all the complexes were determined. The nitric oxide reactivity of the complexes was studied in acetonitrile solvent. The formation of thermally unstable [CuII-NO] intermediate on reaction of the complexes with nitric oxide in acetonitrile solution was observed prior to the reduction of copper(ii) centres to copper(i). The reduction was found to result with a simultaneous mono- and di-nitrosation at the secondary amine sites of the ligand. All the nitrosation products were isolated and characterized. The ratio of the yield of mono- and di-nitrosation product was found to be dependent on the N-substitution present in the ligand framework.