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Tannins Muhammad Tanveer Khan
Introduction ,[object Object]
Definition ,[object Object],[object Object],[object Object]
Physical Properties ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Chemical properties ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
(i) Precipitation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],(ii) Anti-oxidizing properties Because of accumulation of OH group on small size nucleus, these agents have anti-oxidant nature.
(iii) Astringent ,[object Object],(iv) Carcinogenicity Prolong use of  tannin containing plant material is hazardous because it causes cancer. Habitual use of Areca catechu can cause oral and esophageal cancer.
(v) Reaction with salts (vi) Reaction with potassium ferricyanide and ammonia
Importance of tannins ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Industrial Uses: Ink manufacture Vegetable tanning Preservatives Biological Activities: Inhibition of lipid per oxidation Decrease in blood urea nitrogen content Inhibition of plasmin Lipolysis in fat cells
Chemical Classification ,[object Object],Tannins Hydrolysable tannins Condensed tannins Complex tannins
(i) Hydrolysable tannins ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],Types: Hydrolysable tannins Gallitannins Ellagitannins
* Slowly soluble in water. * Present in plants in open and ring forms as Hexa hydroxy diphenic acid. * Rapidly soluble in water. * Free Gallic acid, in plant, is converted to gluco Gallitannins. Properties Upon acid hydrolysis of Ellagitannins, Ellagic acid is produces. Upon acid hydrolysis of Gallitannins, Gallic acid is produces. Hydrolysis Pomegranate Eucalyptus Rhubarb Clove Hamamelis  Occurrence Ellagitannins Gallitannins
(ii) Condensed tannins ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],Examples: Hamamelis Cinchona Cinnamon When heated with acids, these are self condensated, polymerized and converted to insoluble red colored complexes, called  Phlobaphenes.
(iii) Complex tannins ,[object Object],[object Object],[object Object],[object Object],[object Object]
2nd Classification ,[object Object],[object Object],[object Object],[object Object],Tannins True tannins Pseudo tannins
Molecular weight is less than true tannins. Molecular weight is 1000-5000 Phenolic compounds of plant origin that don't convert animal hide to leather but do give positive Gold beater’s skin test, are called pseudo tannins. Polyhydroxy phenolic compounds which convert animal hide to leather by precipitating proteins and give positive Gold beater’s skin test, are called true tannins.  Pseudo tannins True tannins
Identification tests ,[object Object],[object Object]
Identification tests ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Identification tests ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Identification tests ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Identification tests ,[object Object],[object Object],[object Object],[object Object]
a) Hamamelis ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
b) Catechu ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
c) Nutt gall ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Tannins

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  • 8. (v) Reaction with salts (vi) Reaction with potassium ferricyanide and ammonia
  • 9.
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  • 11.
  • 12.
  • 13. * Slowly soluble in water. * Present in plants in open and ring forms as Hexa hydroxy diphenic acid. * Rapidly soluble in water. * Free Gallic acid, in plant, is converted to gluco Gallitannins. Properties Upon acid hydrolysis of Ellagitannins, Ellagic acid is produces. Upon acid hydrolysis of Gallitannins, Gallic acid is produces. Hydrolysis Pomegranate Eucalyptus Rhubarb Clove Hamamelis Occurrence Ellagitannins Gallitannins
  • 14.
  • 15.
  • 16.
  • 17.
  • 18. Molecular weight is less than true tannins. Molecular weight is 1000-5000 Phenolic compounds of plant origin that don't convert animal hide to leather but do give positive Gold beater’s skin test, are called pseudo tannins. Polyhydroxy phenolic compounds which convert animal hide to leather by precipitating proteins and give positive Gold beater’s skin test, are called true tannins. Pseudo tannins True tannins
  • 19.
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  • 22.
  • 23.
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