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Terpenes (basics)

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presentation of terpenes

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Terpenes (basics)

  1. 1. Terpenes By : mohammed kassim mohammed ghassan yahya abd_alkhaliq mostafa monqeth
  2. 2. General information  Terpenes are unsaturated compounds formed by joining together isoprene units.  Terpenes are components of a wide variety of fruit and aromas.  Terpene derivatives are responsible for the special aroma of spices.
  3. 3. Terpenes  The name ‘terpene’ is derived from the Greek word ‘terebinth’.  Terebinth is a type of pine tree from which terpene-containing resins are obtained.
  4. 4. What are terpenes?  Natural organic compounds.  Components of a variety of fruit and and aromas.  Used in perfumes, essential oils and medicines.
  5. 5. Therapeutic Uses of terpenes  Antidepressant – Relieves symptoms of depression.  Antifungal – Inhibits the growth of fungus  Anti-Inflammatory – Reduces inflammation.  Gastro-esophageal Reflux –  Reduces acid reflux.  Immune stimulant –  Stimulates the immune system.
  6. 6. Spices contain terpenes  Terpenes in plants can be oxidized to produce the compounds responsible for the special aroma of spices.  Terpenes containing oxygen or other functional groups are known as ‘terpenoids’.  Common spices containing terpenes include cloves, cinnamon and ginger.
  7. 7. Terpenes are unsaturated  Terpenes are unsaturated compounds.  All terpenes are built up from units of isoprene.
  8. 8. Building terpenes from isoprene Isoprene units can be linked:  1- head to tail to form linear terpenes  2- in rings to form cyclic terpenes.
  9. 9. Isoprene: the main unit to form terpene C CH3 CH2 CH CH2 Head Tail Isoprene (2-methylbuta-1,3-diene) = One isoprene unit contains five carbon atoms Isoprene is the common name for 2-methylbuta-1,3-diene
  10. 10. Types of terpenes  It’s could be monoterpenes or cyclicterpenes or diterpenes  Terpenes can oxidised to a form terpenoid
  11. 11. Myrcene – a linear terpene • Myrcene is a component of plants, including bay, and thyme. Head TailHead Tail C CH3 CH3 CH CH2 C CH2 CH2 CH CH2 Chemical formulaC10H16 uses perfumery industry
  12. 12. Limonene – a cyclic terpene CH2 CH2 C CH CH2 CH C CH2CH3 CH3 Limonene (skin of citrus fruits) Chemical formula C10H16 Uses in cosmetic pro-ducts , in food manufacturing
  13. 13. Menthol – a cyclic terpenoid CH2 CH CH CH2 CH CH2 CH3 OH CH CH3CH3 Menthol (peppermint) This terpene has been oxidised to a terpenoid uses local anesthetic, relieve throat irritation Chemical formulaC10H20O
  14. 14. Absinthe – a cyclic terpenoid CH2 C CH CH C CH2 O CH3 CH CH3CH3 Thujone (Absinthe) This terpene has been oxidised to a terpenoid Chemical formula C10H16O uses Perfumery, Artemisia absinthium L.
  15. 15. Camphor – a cyclic terpenoid CH2 CH2 CH C C C CH2 O CH3 CH3 CH3 Camphor (Camphor tree) Chemical formula C10H16O Side effect Uses anesthetic , antimicrobial Camphor tree
  16. 16. α-Selinene – a cyclic terpene 3 isoprene units 15 carbon atoms CH2 CH2 CH2 CH C CH2 CH3 C C C CH2 CH2 CH2 CH2 CH3 H α-Selinene Chemical formula C15H24 Uses reduce blood pressure
  17. 17. β-carotene – a linear terpene 8 isoprene units 40 carbon atoms CH2 CH2 CH2 C C C CH3CH3 CH CH C CH CH CH C CH CH CH CH C CH CH CH C CH CH C C CH2 CH2 CH2 C CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 β- c a r o t e n e Chemical formula C40H56 Uses decrease asthma symptoms, prevent heart disease
  18. 18. Side effects of terpenes  Terpenes have not any side effect because it’s presence in plants & give it’s the special aromatic odor  However , terpenes like any compound else shouldn’t used excessively because that reduce the advantage of it .
  19. 19. Summary  Terpenes are unsaturated compounds formed by joining together isoprene units.  Terpenes are components in a wide variety of fruit and floral flavours and aromas.  Terpenes can be oxidised within plants to produce the compounds responsible for the distinctive aroma of spices.
  20. 20. Refrences  http://theleafonline.com/c/science/2014/09/terpene- profile-limonene/  https://www.medicaljane.com/category/cannabis- classroom/terpenes/#terpenes-in-cannabis  http://emedicine.medscape.com/article/818675-overview
  21. 21. Done & Done 

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