5-Nonanone, or dibutyl ketone, is the organic compound with the formula (CH 3 CH 2 CH 2 CH 2) 2 CO. This colorless liquid is a symmetrical ketone. [2] 5-Nonanone, which is potentially of interest as a diesel fuel, can be produced from levulinic acid, which can be produced from fructose.

5-Nonanone | C9H18O | CID 10405 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Other names: Butyl ketone; Dibutyl ketone; Nonan-5-one; (n-C4H9)2CO; di-n-Butylketone; 5-Oxononane Permanent link for this species. Use this link for bookmarking this species for future reference.

Aldrich-136948; 5-Nonanone 0.98; CAS No.: 502-56-7; Synonyms: Dibutyl ketone; Valerone; Linear Formula: CH3(CH2)3CO(CH2)3CH3; Empirical Formula: C9H18O; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.

5-Nonanone. CH3(CH2)3CO(CH2)3CH3. Synonyms: Dibutyl ketone, Valerone. CAS 502-56-7. Molecular Weight 142.24. Browse 5-Nonanone and related products at Merck.

Other names: Butyl ketone; Dibutyl ketone; Nonan-5-one; (n-C4H9)2CO; di-n-Butylketone; 5-Oxononane Permanent link for this species. Use this link for bookmarking this species for future reference.

In typical processes, the gaseous effluent from the second-stage oxidation is cooled and fed to an absorber to isolate the MAA as a 20—40% aqueous solution. The MAA may then be concentrated by extraction into a suitable organic solvent such as butyl acetate, toluene, or dibutyl ketone.

5-Nonanone, or dibutyl ketone, is the organic compound with the formula (CH3CH2CH2CH2)2CO. This colorless liquid is a symmetrical ketone.

This report presents a cost analysis of Dibutyl Ketone (DBK) production from levulinic acid. The process examined is similar to the one proposed by the University of Wisconsin-Madison.

Ketones, such as 5-Nonanone, are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone.