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  2. Limonene - Wikipedia

    en.wikipedia.org/wiki/Limonene

    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. [3] Limonene takes its name from Italian limone ("lemon"). [4] Limonene is a chiral molecule, and biological sources produce one enantiomer: the principal industrial source, citrus fruit ...

  3. Perillyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Perillyl_alcohol

    Perillyl alcohol and its precursor limonene are naturally occurring monocyclic terpenes derived from the mevalonate pathway in plants. Perillyl alcohol can be found in the essential oils of various plants, such as lavender, lemongrass, sage, and peppermint. [1] It has a number of manufacturing, household, and medical applications.

  4. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    In plants, VirA is a protein histidine kinase which senses certain sugars and phenolic compounds. These compounds are typically found from wounded plants, and as a result VirA is used by Agrobacterium tumefaciens to locate potential host organisms for infection. [95]

  5. Canarium luzonicum - Wikipedia

    en.wikipedia.org/wiki/Canarium_luzonicum

    The constituents include phellandrene, limonene, elemol, elemicin, terpineol, carvone, and terpinolene. The seed kernels are used for food, both raw and cooked. An edible oil can be extracted from the seeds, and the pulp can be stewed but is somewhat insipid. The young shoots can be boiled and eaten as a vegetable. [3]

  6. Monoterpene - Wikipedia

    en.wikipedia.org/wiki/Monoterpene

    Many monoterpenes are volatile compounds and some of them are well-known fragrants found in the essential oils of many plants. [12] For example, camphor, citral, citronellol, geraniol, grapefruit mercaptan, eucalyptol, ocimene, myrcene, limonene, linalool, menthol, camphene and pinenes are used in perfumes and cosmetic products.

  7. File:Limonene Biosynthesis (coloured).svg - Wikipedia

    en.wikipedia.org/wiki/File:Limonene_Biosynthesis...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  8. Plant - Wikipedia

    en.wikipedia.org/wiki/Plant

    In seed plants (gymnosperms and flowering plants), the sporophyte forms most of the visible plant, and the gametophyte is very small. Flowering plants reproduce sexually using flowers, which contain male and female parts: these may be within the same ( hermaphrodite ) flower, on different flowers on the same plant , or on different plants .

  9. Carvone - Wikipedia

    en.wikipedia.org/wiki/Carvone

    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 ...