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Piperidine is used as a solvent and as a base. The same is true for certain derivatives: N-formylpiperidine is a polar aprotic solvent with better hydrocarbon solubility than other amide solvents, and 2,2,6,6-tetramethylpiperidine is a highly sterically hindered base, useful because of its low nucleophilicity and high solubility in organic ...
Piperidine, a cyclic six-membered amine that results from hydrolysis of piperine; Piperic acid, the carboxylic acid also derived from hydrolysis of piperine; Capsaicin, the active piquant chemical in chili peppers; Allyl isothiocyanate, the active piquant chemical in mustard, radishes, horseradish, and wasabi
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.
Piperidine, the parent compound of piperidine alkaloids Piperidine alkaloids are naturally occurring chemical compounds from the group of alkaloids , which are chemically derived from piperidine . Alkaloids with a piperidine building block are widespread and are usually further subdivided according to their occurrence and biogenetic origin.
The chemical is part of the piperidine family, [1] along with many pharmaceuticals and alkaloids such as piperine, which gives black pepper its spicy taste. Trade names include Bayrepel and Saltidin among others. The compound was developed by the German chemical company Bayer in the 1980s [6] and was given the name Bayrepel.
The compounds with the very highest chlorine numbers (e.g. octachlorodibenzo-p-dioxin) are, however, so poorly soluble that this hinders their bioaccumulation. [85] Bioaccumulation is followed by biomagnification. Lipid-soluble compounds are first accumulated to microscopic organisms such as phytoplankton (plankton of plant character, e.g. algae).
POPs have low solubility in water but are easily captured by solid particles, and are soluble in organic fluids (oils, fats, and liquid fuels). POPs are not easily degraded in the environment due to their stability and low decomposition rates. Due to this capacity for long-range transport, POP environmental contamination is extensive, even in ...