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1,2,5-Trimethylpyrrole is used as an organic chemical synthesis intermediate.
Bruce Beaver; Yun Teng; Philippe Guiriec; Philippe Hapiot; P.Neta. Mechanisms of oxidation of 1,2,5-trimethylpyrrole:? Kinetic, spectroscopic, and electrochemical studies. J. Phys. Chem. A. 1998, 102,(30), 6121-6128.
Francois Terrier; Elyane Kizilian; Jean Claude Halle; Erwin Buncel. 4,6-Dinitrobenzofuroxan: a stronger electrophile than the p-nitrobenzenediazonium cation and proton. J. Am. Chem. Soc. 1992, 114,(5), 1740-1742.
Hazard Statements: H226-H315-H319-H335
Flammable liquid and vapour. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P260-P201-P280a-P304+P340-P405-P501a
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.