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Carvone may be synthetically prepared from limonene by first treating limonene nitrosyl chloride. Heating this nitroso compound gives carvoxime. Treating carvoxime with oxalic acid yields carvone. [14] This procedure affords R-(−)-carvone from R-(+)-limonene. The major use of d-limonene is as a precursor to S-(+)-carvone. The large scale ...
R)-PAC is widely synthesized by fermentation of benzaldehyde and dextrose. In this process, colonies of yeast (in particular, strains such as Candida utilis , Torulaspora delbrueckii , or Saccharomyces cerevisiae ) are cultivated and added to a broth of water, dextrose , and the enzyme pyruvate decarboxylase in a vat.
Thus, the two substrates of this enzyme are (-)-trans-carveol and NADP +, whereas its 3 products are (-)-carvone, NADPH, and H +. This enzyme belongs to the family of oxidoreductases , specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor.
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CAS Number. 362483-06-5 ... C 10 H 12 O 3 Molar mass: 180.20 g/mol ... is a terpenoid formed by metabolism of carvone in humans. [1] References
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[1] [2] It is also used in chemical synthesis as a precursor to carvone and as a renewables-based solvent in cleaning products. [1] The less common (-)- isomer has a piny , turpentine -like odor, and is found in the edible parts of such plants as caraway , dill , and bergamot orange plants.