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Prepared By :
Jeetendra Yadav Ishant Subedi
Durga Ghimire Kamal Timsina
Kiran Gautam Jayakarna Budha
Introduction : .
Fungicides are chemicals that have the
ability to reduce or prevent the damage caused by
fungi in plants and their products.
Fungicides are
biocidal chemical compounds used to kill parasitic fungi
or their spores.
Classification of fungicides
1. On the basis of use
Protective
Curative
A. Protective fungicides : .
They prevent fungal infection
by sporocidal activity.. E.g. Sulphur
B. Curative fungicides :
It penetrate cuticle and kill
young fungal mycelium growing in the epidermis and
this prevents further development of fungal growth.
E.g. Organomercurials
C. Eradicant fungicides : .
They are agents that make
control of fungus even after the symptoms become
visible and that kill both newly developed spores and
the mycelium.
E.g. Systemic fungicides
2. On the basis of sources of raw material
A. Inorganic fungicides :
It includes sulfur powder, lime
sulfur, copper sulfate, mercuric chloride etc…
B. Organic fungicides :
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Chemistry, use, and mode of action of
1.Carbendazim
2.Carboxin
3.Captan
4.Tridemorph
5.Copper oxychloride
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1. Carbendazim :
IUPAC Name
Methyl 1H-benzimidazol-2-ylcarbamate
Other Names
Mercarzole
Carbendazole
Properties
Chemical formula : C9H9N3O2
Melting Point (M.P) : 302-307˚ C
Uses .
It is used to control plant diseases in cereals, and
fruit including citrus, bananas, strawberries,
pineapple etc..
Mostly used to control Botrytis, Gloeosporium rots,
powdery mildews and apple scab
Mode of action
Carbendazim works by inhibiting the development
of fungi probably by interfering with spindle
formation at mitosis (cell division).
affects the nervous system through their main
metabolite, carbon disulfide.
2. Carboxin : .
IUPAC Name :
6-methyl-N-phenyl-2,3-dihydro-1,4-oxathiine-5-carboxamide
Others Name :
Vitavax
Kisvax
Carbathiin etc…
Properties :
• It is an off-white crystals
• Systemic fungicide and seed protectant.
• soluble in water
Mode of action .
The dioxide analogue of carboxin inhibit
succinate cytochrome C reductase,
succinate co-enzyme Q reductase or
succinate reductase.
Beside this monoxide analogue also
inhibit these enzymes.
3. Captan : .
IUPAC Name :
2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione
Others Name :
Captaf
Hexacap
Captab
Properties .
Odorless
white crystalline powder
Melting point 172.5˚ C
Slightly soluble in ethylene dichloride
Noncorrosive in nature
Uses :
Captan is predominantly used in agriculture as a
fungicide on a wide variety of fruits, vegetables, and
ornamentals on plant seeds, and also on food crop
packaging boxes.
Captan is also used in cosmetics
pharmaceuticals
oil-based paints
wallpaper paste
Plasticizers
rubber stabilizers
textiles etc……
Mode of action .
Captan is non specific thiol rectant with protective
and curative action that works by inhibiting
respiration of numerous species of fungi and
bacteria
The mechanism of action may involve the
degradation of captan in to the short lived thio
phosgene which is highly reactive with thiols and
other functional group
4. Tridemorph .
IUPAC Name
2,6-Dimethyl-4-tridecylmorpholine
Molecular Formula
C19H39NO
Properties
Boiling point : 134˚ C
Yellow oily liquid
Uses : .
fungicide used to control Erysiphe graminis
moderately hazardous
Mode of action
Inhibit protein and RNA synthesis
Inhibit lipid synthesis and
Often inhibit sterol biosynthesis
5. Copper oxychloride .
IUPAC Name
Dicopper Chloride Trihydroxide
Properties
Not flammable
Highly toxic fungicide
Insoluble in water
Uses :
Copper Oxychloride is for the control of fungal and
bacterial diseases in fruit and vegetable crops, citrus,
stone fruit, pome fruit and ornamentals.
Key Features and Benefits .
• Economical control of a wide range of fungal and
bacterial diseases in many crops and situations
• pH neutral product and ultra-fine particle size with
majority of particles less than or equal to 2-micron
diameter
• Free flowing product for easy mixing and
application
• Can be applied in tank mixes with a wide range of
other chemicals and/or fertilisers.
Mode of action : .
Interfers with the enzyme system of
mycelium and spores.
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