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  2. Limonene - Wikipedia

    en.wikipedia.org/wiki/Limonene

    Limonene (/ ˈ l ɪ m ə n ˌ iː n /) is a colorless liquid aliphatic hydrocarbon classified as a cyclic monoterpene, and is the major component in the essential oil of citrus fruit peels. [1] The (+)- isomer , occurring more commonly in nature as the fragrance of oranges, is a flavoring agent in food manufacturing.

  3. 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 ...

  4. Green solvent - Wikipedia

    en.wikipedia.org/wiki/Green_solvent

    D-Limonene, a terpene. Solvents in a diverse class of natural substances called terpenes are obtained by extraction from certain parts of plants. All terpenes are structurally presented as multiples of isoprene with the gross formula (C 5 H 8) n. D-limonene, a monoterpene, is one of the best known solvents in this class, as is turpentine.

  5. Orange oil - Wikipedia

    en.wikipedia.org/wiki/Orange_oil

    Orange oil, particularly its primary component d-limonene, is registered with the EPA as an active ingredient in products for the extermination of drywood termites, Formosan termites, and other structural pests. [8] It is a common alternative to traditional fumigation methods due to its lower toxicity and the convenience of local chemical ...

  6. D-limonene - Wikipedia

    en.wikipedia.org/?title=D-limonene&redirect=no

    This page was last edited on 13 July 2005, at 13:37 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

  7. Monoterpene - Wikipedia

    en.wikipedia.org/wiki/Monoterpene

    Limonene and perillyl alcohol are used in cleaning products. [13] [14] Many monoterpenes are used as food flavors and food additives, such as bornyl acetate, citral, eucalyptol, menthol, hinokitiol, camphene and limonene. [15] [16] Menthol, hinokitiol and thymol are also used in oral hygiene products. Thymol also has antiseptic and disinfectant ...

  8. Autoignition temperature - Wikipedia

    en.wikipedia.org/wiki/Autoignition_temperature

    The autoignition temperature or self-ignition temperature, often called spontaneous ignition temperature or minimum ignition temperature (or shortly ignition temperature) and formerly also known as kindling point, of a substance is the lowest temperature at which it spontaneously ignites in a normal atmosphere without an external source of ignition, such as a flame or spark. [1]

  9. Pyrophoricity - Wikipedia

    en.wikipedia.org/wiki/Pyrophoricity

    The creation of sparks from metals is based on the pyrophoricity of small metal particles, and pyrophoric alloys are made for this purpose. [2] Practical applications include the sparking mechanisms in lighters and various toys, using ferrocerium; starting fires without matches, using a firesteel; the flintlock mechanism in firearms; and spark testing ferrous metals.