Piperidinas

Stability Volatile
Applications In the presence of sugars, lysine, similarly to asparagine and phenylalanine, can undergo carbonyl-assisted decarboxylative deamination reaction to generate pent-4-en-1-amine, the counterpart of acrylamide.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Stadler, R., et al.: Chem. Res. Toxicol., 16, 1242 (2003), Stadler, R., et al.: J. Agric. Food Chem., 52, 5550 (2004),

Applications N-Benzyl-3-hydroxypiperidine has been used as a reactant in the preparation of optically active azidopiperidines.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Cochi, A., et. al.: Eur. J. Org. Chem., 2012, 2023 (2012)

Applications 4-Benzyl-4-piperidinol, is a building block used for the synthesis of various compounds, having therapeutic properties, such as synthesis of 4-Benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.
References Ting, P. C., et al.: Bioorg. Med. Chem. Lett., 20, 5004 (2010);

Stability Hygroscopic
Applications Mixture of 6R-Hydroxyhyoscyamine (H942815) and 6S-Hydroxyhyoscyamine (H942820). A derivative of Hyoscyamine (H674300).

(R)-(-)-1-Boc-3-(hydroxymethyl)piperidine is used as pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item cod