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Terpenes
By : mohammed kassim
mohammed ghassan
yahya abd_alkhaliq
mostafa monqeth
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.
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.
What are terpenes?
 Natural organic compounds.
 Components of a variety of fruit and
and aromas.
 Used in perfumes, essential oils and
medicines.
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.
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.
Terpenes are unsaturated
 Terpenes are unsaturated compounds.
 All terpenes are built up from units of
isoprene.
Building terpenes from isoprene
Isoprene units can be linked:
 1- head to tail to form linear terpenes
 2- in rings to form cyclic terpenes.
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
Types of terpenes
 It’s could be monoterpenes or
cyclicterpenes or diterpenes
 Terpenes can oxidised to a form
terpenoid
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
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
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
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.
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
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
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
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 .
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.
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
Done & Done 

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Terpenes (basics)

  • 1. Terpenes By : mohammed kassim mohammed ghassan yahya abd_alkhaliq mostafa monqeth
  • 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. 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. What are terpenes?  Natural organic compounds.  Components of a variety of fruit and and aromas.  Used in perfumes, essential oils and medicines.
  • 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. 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. Terpenes are unsaturated  Terpenes are unsaturated compounds.  All terpenes are built up from units of isoprene.
  • 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. 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. Types of terpenes  It’s could be monoterpenes or cyclicterpenes or diterpenes  Terpenes can oxidised to a form terpenoid
  • 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. 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. 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. 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. 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. 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. 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. 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. 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.
  • 21. Done & Done