The chemistry surrounding the pyrolysis of N,NЈ-ethylenebisstearimide (EBS) compacted with iron powder is described for the first time. Heat treatment is carried out in a 5 vol pct hydrogen atmosphere (balance nitrogen) over the 100°C to 850°C range. The exhaust from the furnace is monitored by Fourier transform infrared and dispersive ultraviolet absorption spectroscopy; condensable materials are analyzed by gas chromatography/mass spectrometry (GC/MS). A wide range of analytes emitted from the preceding process were characterized. The aliphatic CH stretch in the 3000 to 2700 cm Ϫ1 range and the asymmetric CO stretch in gaseous CO 2 at 2350 cm Ϫ1 are excellent indicators of the extent of delubrication. A bimodal CO emission phase is observed in the temperature window between delubrication and sintering. Three major large molecule reaction products, along with five minor compounds, are identified by GC/MS. A preliminary reaction mechanism is inferred based on product analysis and known organic chemistry. It appears that hydrolysis of EBS competes with ␥-H abstraction yielding an N-vinyl amide and stearamide, which undergoes further reaction. Hydrolysis affords stearic acid, which decarboxylates to heptadecane, and 2-heptadecyl-4,5-dihydroimidazole via ring closure of the corresponding amino-amide.