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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. 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.

  5. Terpene - Wikipedia

    en.wikipedia.org/wiki/Terpene

    These include the C 13-norisoprenoid 3-oxo-α-ionol present in Muscat of Alexandria leaves and 7,8-dihydroionone derivatives, such as megastigmane-3,9-diol and 3-oxo-7,8-dihydro-α-ionol found in Shiraz leaves (both grapes in the species Vitis vinifera) [35] or wine [36] [37] (responsible for some of the spice notes in Chardonnay), can be ...

  6. Here's How to Use the USDA's Plant Hardiness Zone Map - AOL

    www.aol.com/handy-map-tells-plants-thrive...

    The hardiness zone map is not a guarantee your plant will survive. It's important to understand that the USDA hardiness zone is an indication of which plants are most likely to thrive in a location.

  7. 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 ...

  8. Limonin - Wikipedia

    en.wikipedia.org/wiki/Limonin

    Limonin is a limonoid, and a bitter, white, crystalline substance found in citrus and other plants. It is also known as limonoate D-ring-lactone and limonoic acid di-delta-lactone . Chemically, it is a member of the class of compounds known as furanolactones .

  9. Limonoid - Wikipedia

    en.wikipedia.org/wiki/Limonoid

    Limonoids are phytochemicals of the triterpenoid class which are abundant in sweet or sour-scented citrus fruit and other plants of the families Cucurbitaceae, Rutaceae, and Meliaceae. [1] Certain limonoids are antifeedants such as azadirachtin from the neem tree. [2] Chemically, the limonoids consist of variations of the furanolactone core ...