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  2. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    The compound was named heliotropin after the 'cherry pie' notes found in the heliotrope flower's fragrance (even though the chemical is not present in the flower's true aroma). [10] Perfumers began to use the fragrance for the first time by the early 1880s. [ 11 ]

  3. Fragrance extraction - Wikipedia

    en.wikipedia.org/wiki/Fragrance_extraction

    Organic solvent extraction is the most common and most economically important technique for extracting aromatics in the modern perfume industry. Raw materials are submerged and agitated in a solvent that can dissolve the desired aromatic compounds. Commonly used solvents for maceration/solvent extraction include hexane, and dimethyl ether.

  4. Aroma compound - Wikipedia

    en.wikipedia.org/wiki/Aroma_compound

    Fragrance bottles. An aroma compound, also known as an odorant, aroma, fragrance or flavoring, is a chemical compound that has a smell or odor.For an individual chemical or class of chemical compounds to impart a smell or fragrance, it must be sufficiently volatile for transmission via the air to the olfactory system in the upper part of the nose.

  5. Rose oxide - Wikipedia

    en.wikipedia.org/wiki/Rose_oxide

    Rose oxide is an organic compound of the pyran class of monoterpenes.The compound has a cis- and a trans-isomer, each with a (+)- and (−)-stereoisomer, but only the (−)-cis isomer (odor threshold 0.5 ppb) is responsible for the typical rose (floral green) fragrance.

  6. Furaneol - Wikipedia

    en.wikipedia.org/wiki/Furaneol

    Furaneol, or strawberry furanone, is an organic compound used in the flavor and perfume industry. It is formally a derivative of furan. It is a white or colorless solid that is soluble in water and organic solvents. [2]

  7. Farnesol - Wikipedia

    en.wikipedia.org/wiki/Farnesol

    Farnesol is a natural 15-carbon organic compound which is an acyclic sesquiterpene alcohol. Under standard conditions, it is a colorless liquid. It is hydrophobic, and thus insoluble in water, but miscible with oils. As the pyrophosphate ester, farnesol is a precursor to many terpenes and terpenoids. [1]

  8. Nonanal - Wikipedia

    en.wikipedia.org/wiki/Nonanal

    Nonanal is an organic compound with the chemical formula CH 3 (CH 2) 7 CHO. It is one of several isomers, all are colorless oil. The nonanals are classified as aldehydes. The linear nonanal is produced commercially by the hydroformylation of 1-octene. It is used as a fragrance. [2]

  9. Helional - Wikipedia

    en.wikipedia.org/wiki/Helional

    Helional (from heliotropin, from which is it commonly derived) is a chemical compound used as a perfume in soap and laundry detergent. Chemically it is an aldehyde with a hydrocinnamaldehyde motif; a structural element which is present in a number of other important commercial fragrances and odorants.