Rothkopf, G. S. et al. published their research in JAOCS, J. Am. Oil Chem. Soc. in 1984 | CAS: 25560-00-3

3-(2-Methylpiperidin-1-yl)propan-1-amine (cas: 25560-00-3) belongs to piperidine derivatives. The piperidine moiety constitutes an important building block for the synthesis of a variety of bioactive natural products, alkaloids and other drugs. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N鈥揌 bond in an axial position, and the other in an equatorial position.Application In Synthesis of 3-(2-Methylpiperidin-1-yl)propan-1-amine

Structure-biodegradability correlations among xenobiotic industrial amines was written by Rothkopf, G. S.;Bartha, R.. And the article was included in JAOCS, J. Am. Oil Chem. Soc. in 1984.Application In Synthesis of 3-(2-Methylpiperidin-1-yl)propan-1-amine This article mentions the following:

Using acclimated sewage sludge enrichment cultures, 60 amines with potential uses in industrial processes were evaluated for their biodegradability. Biodegradation was measured as cell protein yield with 0.05% amine serving as the sole source of C, N, and energy in a mineral solution Inhibitory properties of the amines, measured by their ability to decrease protein yield on a glucose medium, were unrelated to biodegradability. Under the specified test conditions, all amines that contained tertiary C atoms were recalcitrant. Ring N-substituted heterocyclics were readily degraded, but ring C-substituted piperidines, with the exception of pipecolinic聽acid聽聽[535-75-1] were not. When amines lacked other functional groups, tertiary amino groups hindered degradation Amines with alkyldiamine moieties shorter than Pr did not serve as growth substrates. Predictive generalizations of this type about biodegradability serve as an aid in selecting environmentally safe compounds for industrial processes. In the experiment, the researchers used many compounds, for example, 3-(2-Methylpiperidin-1-yl)propan-1-amine (cas: 25560-00-3Application In Synthesis of 3-(2-Methylpiperidin-1-yl)propan-1-amine).

3-(2-Methylpiperidin-1-yl)propan-1-amine (cas: 25560-00-3) belongs to piperidine derivatives. The piperidine moiety constitutes an important building block for the synthesis of a variety of bioactive natural products, alkaloids and other drugs. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N鈥揌 bond in an axial position, and the other in an equatorial position.Application In Synthesis of 3-(2-Methylpiperidin-1-yl)propan-1-amine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem