INORGANIC INSECTICIDES
Arsenic
compounds:
In an arsenical compound, the total arsenic content and
the water soluble arsenic content are of importance, the water solubility of
arsenic may result in entering the foliage and causing burning injury to
plants, and hence water insoluble compounds are preferred for insect control.
Arsenates are more stable and safe for application on plants then arsenites. Arsenites
are mainly used in poison baits since they are phytotoxic. However arsenates
are less toxic to insects then arsenites. In insects arsenates cause
regurgitation, torpor (sluggishness) and quiescence. Disintegration of
epithelial cells of the midgut and clumping of the chromatin of the nuclei are
the effects noticed in poisoned insects. Slow decrease in oxygen consumption is
also evident and kill of the insect is primarily due to the inhibition of respiratory
enzymes. Water soluble arsenic causes wilting followed by browning and shriveling
of the tissue.
1. Calcium arsenate: It was first used by about
1906 as an insecticide. It is a white flocculent power, formulated as a dust of
25 to 30% metallic arsenic equivalent. Dosage – Calcium arsenate at 0.675 to
1.350 kg with equal quantity of slaked lime in 450 litres of water. LD50.for
mammals oral – 35 to 100. Being a stomach poison it was mainly used for control
of leaf eating insects.
2. Lead arsenate: It
was first used as in insecticide in 1892 for the control of gypsy moth. It is a
stomach poison with little contact action LD50.for rat oral 10-100, dermal 2400
mg/kg. . It is rarely used as dust. 450 g to 1800 g of load arsenate is diluted
with 200-240 litres of water. An equal quantity of hydrated lime is some time
added to prevent phytotoxicity to tender foliage. In baits it is used at 450 or900
g in 1200 g to 45000 g of carrier such as wheat bran or rice husk respectively.
3.
Arsenite: Paris green:It is a double salt of copper acetate and copper
arsenite. It was first used in 1867 for the control of Colorado potato beetle, Leptinotarsa
decemlineata. It is now used as bait for the control of slugs. LD50for rat
oral- 22 mg/kg.Very good against termites.
Flourine Compounds: These
compounds were used since 1890. They are principally stomach poisons and to a
limited extent contact poisons. The kill is more rapid than that of arsenicals.
Their insecticidal properties are related to the fluorine content and
solubility in the digestive juices of insect. Flouride poisoning produces
spasms, regurgitation, flaccid paralysis and death.
1. Sodium fluoride: It
is a white power. Available in 93 to 99% purity in commercial products. It is
highly phytotoxic and used in poison baits used exclusively against cockroaches,
earwigs, cutworms, grasshoppers etc.
Other inorganic compounds
1. Sulphur: It is
primarily fungicide and acaricide. Formulated as fine dust (90 to 95% a.i with
10% inert material. It is also formulated as wettable powders. Effectiveness increases
with fineness of sulphur particles.
2. Lime sulphur: Aqueous
solution of calcium polysulphide. It is prepared by sulphur solution in calcium
hydroxide suspension, preferably under pressure in the absence of air and is
used against scales, mites, aphids besides powdery mildew.
Properties
§
Affect nervous system causing excitement at
lower doses and paralysis at higher concentration.
§
Not phytoloxic
§
Leave no harmful side effects.
§
Mighly toxic to mammals.
§
Disappear rapidly from the treated surface.So
can be used safely before harvest of the produce.
Insecticides
of plant origin (Botanical Pesticides)
The insecticides of plant origin extracted from seeds,
flowers, leaves, stem and roots, are termed as botanical insecticides.
Insecticides of plant origin unlike synthetic organic insecticides are safer to
use but since they are expensive and lack residual toxicity, their use has been
limited in the country.
In nature more than, 2400 plant species are
reported to have pesticidal properties. The important families having
pesticidal properties are
Plant family
|
No. of plant having pesticidal property
|
Meliaceae
|
> 500
|
Myrtaceae
|
72
|
Asteraceae
|
70
|
Euphorbiaceae
|
65
|
Leguminosae
|
60
|
Fabaceae
|
55
|
1)
Neem (Azadirachta indica)
Perennial tree distributed in tropical, subtropical,
semi-arid and arid zones. It posses medicinal, insecticidal, insect repellent,
antifeedant, growth regulatory, nematicidal and antifungal properties. Neem
seed extract and oil contains a number of components such as Azadirachtin,
salannin, nimbin, epinimbin nimbidin that gives insecticidal, insect repellent,
ovicidal, Antifeedant and growth regulator characters. Azadiractitin disrupts
moulting by antagonizing the insect hormone ecdysone.Azadiractitin Acute oral
LD50 for rat is 5000mg/kg, Acute dermal for rabbit is >2000mg/kg.
Preparation of Neem Seed Kernel Extract (NSKE 5%): Take
50 g of powdered neem seed kernels soak it in one litre of water for 8 hours
and stir the contents often. Squeeze the soaked material repeatedly for better
extraction of the azadirachtin in the aquous suspension. Filter the contents
through muslin cloth. Make the filtrate to one litre. Add 1ml teepol or triton
or sandovit or soap water (2%) and spray.
Prepartion
of Neem Cake Suspension
Soak one kilogram of neem cake in 5 liters of water for 2
days and filter It through muslin cloth. Dissolve 200 g of soft soap in the
filtrate and make upto 10 L of water before spraying. This controls tobacco
cutworm, leaf miners of citrus, groundnut, tomato and beans etc. Dried powder
of neem leaves are used against stored grain insect pests. Leaf extracts showed
insecticidal property against,Plutella xylostella,Aproaerema modicella;
Spodoptera litura etc. Desert locust Schistocerca gregaria avoids
feeding on neem leaves. Neem leaves are found as attractants to white grub Holotrichia
adults. Neem seed/ kernel extract showed insecticidal properties against a
number of sucking pest. Neem oil can be used against storage insect pests @ 1
to 2% and field insects @ (0.2 -0.4%, 1 to 2% 5% or 10% neem oil). Neem products
are safer to honey bees, parasitoids, predators.
Commercial
formulations of neem are available in 10000 ppm, 1500 ppm and 300 ppm the
market. Some of the neem formulations are Margosan, Neemark, Neemrich, Achook,
Bioneem, Neemazal, Neemax, Nimbicidine,Vepacide, Margocide , Neemgold etc
2) Nicotine: Nicotine is found in the leaves of Nicotiana
tabacum and N.rusticafrom 2%
to 14%.Nicotine sulphate has been mainly used as a contact
insecticide with marked fumigant action in the control of sucking insect’sviz.,
aphids, thrips, psyllids, leafminers and jassids. Nicotine sulphate is more
stable and less volatile. It is a nerve poison being highly toxic when absorbed
through the cuticle taken in through the tracheae or when ingested. It affects
the ganglian blocking conduction at higher levels. Nicotine sulphate containing
40% alkaloid, is safer and is more convenient to use and the free alkaloid is liberated
by the addition of soap lime or ammonium hydroxide to the spray solution. Dust
formulation of nicotine sulphate releases nicotine in the presence of moisture.
It is also used in aerosols. Tobacco decoction, useful for controlling aphids,
Thrips etc. can be prepared by boiling 1kg of tobacco waste in 10lts of water
for 30 minutes or steep it in cold water for a day. Then make it up to 30
litres and add about 90gm of soap. Addition of soap improves wetting, spreading
and killing properties. Nicotine does not leave any harmful residue on treated
surface. LD50for rat oral- 50-60 mg/kg.
3) Rotenone: It is extracted from the roots of
Derris plant which many contain 4 to 11% rotenone depending on the variety.
Though rotenone is reported from 68 species of leguminous plants, principal
commercial sources are Derris ellipticaD. Malaccensisfrom Malaysia and Lonchocarupus
utilis andD. uruca from S. America. Rotenone occurs in Derris roots
(4-9%), Lonchocarpus (8-11%).
It is oxidized to non-insecticidal compound in the
presence of light and air and hence rotenone residues are difficult to find
after 5 to 10 days in normal sunlight. Insects poisoned with rotenone show a
steady decline in oxygen consumption followed by paralysis and deaths. It is
very specific being highly toxic to fishes and to most insect species but
almost harmless to warm blooded animals except pigs LD50.to white rat oral-130
to 1500. Dust or spray containing 0.5 to 1.0 per cent and 0.001 to 0.002
percentrotenone are used commercially.
4)
Plumbagin:
Plumbagin is naturally occurring napthoquinone of plant
origin from the roots of Plumbago europea L. (Plumbaginaceae) and
named so in 1828 by Bulong d’ Astafort. Plumbagin is known for its medicinal,
antifertility, antimicrobial, molluscicidal, nematicidal and other
pharmacological properties on diverse fauna. The yield of plumbagin ranges
between 0.5-3.000percent on dry weight basis.
The elucidation of structure of plumbagin and its
synthesis in 1936 led to detailed studies. More recently, its IGR properties viz.,
inhibition of chitin synthetase and ecdysteroid titres have been
demonstrated (Kubo et al., 1982) The cold alcoholic extract (5%) of roots of P.
zeylanica L was toxic to Euproctis fraterna larvae as contact spray.
Contact toxicity of 5% petroleum ether extracts of P. zeylanica root
against Spodoptera litura Fab., Dystercus koenigiiFab.,Dipaphis
erysimi Kalt, Dactynops carthami H.R.L, Coccinella septumpunctata
L was also reported.
5) Pyrethrum: It is extracted from dried flower
heads of Chrysanthemum cinerariaefolium (Asteraceae). The actual
chemical ingredients having insecticidal action are identified as five esters.
They are: Pyrethrin I, Pyrethrin II, cinerins -I and cinerin-II and Jasmoline,
which are predominately found in achenes of flowers from 0.7 to 3 %. The esters
are derived from the,
Two acids – Chrysanthemic acid and Pyrethric acid
Three
alcohols – Pyretholone, Cinerolone and Jasmolone
Active
principles/Esters
Pyrethrin
I = Pyrethrolone + Chrysanthemc acid
Pyrethrin
II = Pyrethrolone + Pyrethric acid
Cinerin
I = Cynerolone + Chrysanthemc acid
Cinerin
II = Cynerolone + Pyrethric acid
Jasmolin
II = Jasmolone + Pyrethric acid
Pyrethrum powder is prepared by grinding the flowers. The
powder mixed with a diluent such as talc or clay is known as pyrethrum dust. It
is prepared just before use. Otherwise it gets deteriorated rapidly. It is also
used as emulsions, solutions, and aerosoles. Pyrethrum is unstable to light,
air moisture and alkali. The residues deteriorate very rapidly after
application. Pyrethrins are powerful contact insecticides but appear to be poor
stomach poisons. A characteristic action of Pyrethroid is the rapid paralysis
or ‘knock down’ effect and substantial recovery that follow it. This recovery
is due to rapid enzymatic detoxification in the insect. To bring about
mortality equivalent to knock down effect three times increase in dosage may be
required. Compounds such as piperonyl butoxide, propyl isome and sulfoxide are
known to inhibit the detoxication enzyme and increase the toxicities of
pyrethroids. These synergists are used at 10 parts to 100 part of pyrethroid.
LD50. for white rat oral-200 dermal for rat-1800. Pyrocon E 2/22 (1 part of
pyrethrin + 10 parts of piperonyl butoxide) is used for the control of coconut
red palm weevil. In household sprays and as a repellent against external
parasites of livestock pyrethrum is useful. It is also mixed with grains in
storage to protect from stored grain pests. Its use alone or in combination
with piperonyl butoxide as food packages has been permitted by the food and
Drug Administration in the U.S.A. and no other chemical has been approved.
Properties
i.
Highly unstable in light, moisture and air.
ii.
Have no residual effect.
iii.
Paralyse by more contact.
iv.
Gains entry through spiracle and cuticle.
v.
Act on central nervous system.
vi.
Having rapid knock down effect.
vii.
Practically no mammalian toxicity.
viii.
Good insecticides against household and cattle pests
Sabadilla:
- It is a alkaloid found in seeds of tropical lily Schoenocaulon officinale (fam: Liliaceae)
- The alkaloid mainly, cevadine and veratridine act as nerve poisions
- It is a primarily contact poision.
- It is harmful to pollinator, honey bees
Ryanodine:
- It is a alkaloid derived from woody stems of South American shrub, Ryania speciosa (Fam; Flacourtaceae)
- Activity: It acts as muscular poison by blocking the conversion of ADP to ATP in strated muscle.
- It acts as slow acting stomach poision and causes insects to stop feeding after they eat it.
- It is reportedly effective against thrips and worms.
- It is used as dust (20-40%)
SYNTHETIC ORGANIC INSECTICIDES
I) Chlorinated Hydrocarbons (Organochlorines): The
plant protection in India owes its growth to the chemicals under this group which
have revolutionized the control of pests. The properties which have lead to
their extensive use are high insecticidal efficacy, long residual action, wide
range of insect susceptibility, cheapness per unit area and available in
different formulations.They are also known as chlorinated synthetics or
chlorinated organics or chlorinated hydrocarbons. The important organochlorines
are
1. DDT: DDT was first synthesized in 1874 by Othmar
Zeidler. In 1939 a Swiss entomologist, Paul Muller, found its insecticidal
property for the first time. This discovery brought the `Nobel Prize' for
medicine to Paul Muller in 1948 for the life saving discovery. Dichloro
Diphenyl Trichloroethane (DDT) is stomach and contact insecticide. It has got
long residual action. It is also non-phytotoxic except to cucurbits. It is not
much effective against phytophagous mites. Due to low cost of DDT and
effectiveness against a variety of insects particularly against house flies and
mosquitoes, it is much popularized but due to long residual life and
accumulation, it is banned in several countries. The acute oral LD50 for rats
is 113-118 mg/kg. It does affect the nervous system preventing normal
transmission of nerve impulses. DDT causes a violent excitatory neurotoxic
system in most insects which are having uncoordinated movement and DDT Jitters
(tremor of the entire body).
2. Hexa Chloro Cyclohexane (HCH): It was first
synthesised by Michael Faraday in the year 1825.The gamma-isomer of BHC has the
insecticidal activity. BHC is a stomach and contact insecticide. It has got slight
fumigant action. It is persistent insecticide. It is non-phytotoxic except
cucurbits .It has been extensively used as soil insecticides particularly to
control termites, white grubs and cutworms. Highly purified product containing
99% of gamma isomer of HCH is known as lindane, this name was proposed in 1949
after Vander Linden, a German chemist who isolated this isomer in 1912. Lindane
is more acute neurotoxicant than DDT results in tremors, ataxia, convolutions,
falling prostration and ultimately leading to death.
II)
Cyclodines
Cyclodienes also act as neurotoxicants which disturb the
balance of sodium and potassium ions within the neuron resulting into tremors,
convulsions, prostration and ultimately the death.
The outstanding characteristic of the cyclodienes is their
longer stability in the soil, resulting in more control of soil inhabiting
insect pests. Some of the compound belonging to this group are chlordane
(1945), aldrin and dieldrin (1948), heptachlor (1949), endrin (1951), mirex
(1954), endosulfan (1956) and chlordecone 1958). Among them aldrin, chlordane
and heptachlor were often in use for termite control as they are most
effective, long lasting and economical insecticides but now banned by GOI.
1)
Aldrin
It is persistent and non-systemic soil insecticide. It is
usually recommended for the control of termites throughout India. Two German
chemists Otto Paul Hermann Diels and Kurt Alder first documented the
Diels-Aldernovel reaction in 1928 for which they were awarded the Nobel Prize
in Chemistry in 1950 for their work Formulations: EC 30%, Granule 5% and Dusts
5%
Trade names: Octalene, Aldrex, Aldrosol, and Aldrite.
LD50 value: 67 mg/kg
2)
Dieldrin
It is persistent and non-systemic insecticide used for
mainly soil inhabiting insect pests. It is also not phytotoxic in recommended
doses.
Formulations: Dust 2%
Trade names: Quintox, Alvit
LD50 value: 46 mg/kg
3)
Heptachlor
It is a non-systemic, contact poison with fumigant action.
It is effective against termites, white grubs, grass hoppers etc
Formulations: EC 20%, and Dust 5%
LD50 value: 100-162 mg/kg
4)
Endosulfan:
It is a non-systemic, contact and stomach poison with
slight fumigant action. It is effective against defoliators, borers, sucking
insects and mites but harmless to honey bees at recommended doses for insect
control. It is highly toxic to fish.
Formulations: EC 35%, Granule 4% and Dusts 4%
Trade
names: Thiodan, Endocel, Endodhan, Endotaf
LD50
value: 80-110 mg/kg
III)
Organophosphates
Organophosphate came to limelight during Second World War.
The biological activity of these compounds was first discovered by W. Lange and
Krueger in 1932. OP compounds as insecticides were mainly due to the work of
Gerhard Schrader in 1937 in Germany. First OP compound TEPP (Tetra Ethyl Pyro
Phosphate) followed by parathion and schradan, the first systemic insecticide.
Organophosphate insecticides have two most important properties such as higher
potency and low residual life. The organophosphates (OPs) inhibit the
cholinesterase (Ch E) enzyme leading to blockage of synaptic transmission of nerve impulses and finally
death.
1)
Malathion
It is a non systemic contact and stomach insecticideand
acaricide of low mammalian toxicity. Hence it is recommended on fruits and
vegetables till a few days prior to harvest. It is also recommended for storage
insects and also for external application for parasites on animals.
Formulations: EC 50 and Dusts 40
Trade names: Cythion and Himala
LD50
value: 2800 mg/kg
2)
Methyl parathion:
It is a contact and stomach poison with slight fumigant
action. It is widely used in for sucking insects and foliage feeders.
Formulations: EC 50 and Dusts 2
Trade names: Folidal, Metacid, Paratox, Dhanumar
LD50 value: 13 mg/kg
3)
Diazinon:
It is a contact persistent insecticide with nematicidal
properties. It is very much useful against household insects such as flies and
cockroaches.It has contact, stomach poison and also fumigant action.
Formulations: EC 20 and 5G
Trade names: Basudin
LD50
value: 300-850 mg/kg .
4)
Dichlorvos (Dimethyl Dichloro Vinyl Phosphate - DDVP)
It is contact poison but due to high vapour pressure it
has got strong penetrating power. It is very effective against hidden insects
due to its fumigation action. It is recommended for leaf miners and leaf
webbers. It brings quick knock down effect. It does not leave toxicresidues. It
is highly toxic to bees. It is acontact and stomach poison with fumigant action.
Formulations:
EC 76 and 5G
Trade
names: nuvan, vapona, Doom, Divap
LD50
value: 56 – 108 mg/kg.
5)
Fenitrothion:
It acts as contact and stomach poison with broad spectrum
activity and a selective acaricide. It is effective against sucking pests
including mealy bugs, borer and mites and external parasites of livestock.
Formulations: EC 35, ULV 0.05 – 0.1 and 5 Dusts
Trade
names: Sumithion, Folithion
LD50
value: 50 – 250 mg/kg.
6)
Quinolphos:
It is contact poison having good penetrating power and It
is having acaricidal properties.It is widely used against caterpillars and
borer on cotton, vegetables and other crops.
Formulations: EC 25 and 5 G
Trade names: Ekalux, Shakthi Quick, Quinguard, Quinaltaf,
Smash, Flash
LD50 value: 62–137 mg/kg.
7)
Phosolone:
It is a non systemic contact insecticide and acaricide,
effective against wide spectrum of species.
Formulations: EC 35
Trade names: Zolone
LD50
value: 135 mg/kg
8)
Chlorpyriphos:
It is a non-systemic contact insecticide very effective
against sucking and chewing insects.It is also recommended against house hold
insect pests. It is widely recommended as seed treatment chemical against white
grub and termites.
Formulations: EC 20
Trade names: Dursban, Chloroban, Durmet, Radar
LD50
value: 135-163 mg/kg
9)
Phosphomidon:
It is a systemic insecticide ha ving low contact action.
It is very effective against sap sucking insect pests. On application it is
absorbed in the plant tissues within 1-3 hours and is translocated more towards
the top. It is less toxic to fish and more toxic to bees.
Formulations:
40 SL
Trade
names: Demecron, Sumidon, Chemidan, Hydan, Phamidon
LD50
value: 17-30 mg/kg
10) Monocrotophos:
It is a systemic insecticide and acaricide with contact
action. It has wide range of susceptibility of insects. It is toxic to bees.
Formulations:
36 SL
Trade
names: Monocil, Nuvacron, Monophos, Monochem, Monostar
LD50 value: 14-23 mg/kg
11)
Methyl demeton:
It is contact and systemic insecticide and acaricide.It is
used against soft bodied insects,
which suck the plant sap.
Formulations: 25 EC
Trade names: Metasystox and Dhanusyatax
LD50
value: 57-106 mg/kg
12)
Dimethoate:
It is
systemic insecticide and acaricide .It is widely used against sucking insect
pests on various crops.
Formulations:
30 EC
Trade
names: Rogor, Celgor, Novogor, Tara 909, roxion
LD50
value: 320-380 mg/kg
13)
Triazophos:
It
has insecticidal, acaricidal and nematicidal properties with trnalaminar
action. It is very
effective
against variety of pests particularly Lepidoptera larvae on fruits and vegetables.
Formulations:
40 EC
Trade
names: Hostathion, Trizocel, Truzo, Suthation
LD50
value: mg/kg
14)
Profenophos:
It is
a broad spectrum non-systemic insecticide.It is recommended against pest of vegetables.
It is highly toxic to birds and fish.
Formulations:
50 EC
Trade
names: Curacron, Celcron, Bolero, Carina, Proven
LD50
value: 358 mg/kg
15)
Acephate:
It is
a systemic andcontact poison.It has low toxicity and safe to environment.
Formulations:
75 SP
Trade
names: Arthane, Starthane, Orthene
LD50
value: 866-945 mg/kg
16)
Phorate:
It is a systemic granular insecticide and also possesses
acaricidal properties. It is very effective against sucking insects and also
against maize borers, cut worms, white grubs etc.
Formulations:
10 G
Trade
names: Thimet
LD50
value: 1.6 – 3.7 mg/kg
CARBAMATES
All carbamates are derivatives of carbamic acid. Many
of the carbamic esters are insecticidal and a few are effective molluscicides
Like organophosphates, the carbamate insecticides interfere in cholinergic
transmission. The carbamate enters the synapse and inhibits the
acetylcholine-esterase as a result the acetylcholine contains to depolarize the
post synaptic membrane, causing prolonged stimulation resulting into the failure
of the nerve or effector tissue. Carbamates have an analogous action, carbamylating
rather than phosphorylating the enzyme and the ChE recovers more readily from
carbamates than from organophosphates. Thus, unlike, organophosphates, they are
known as reversible inhibitors.
1.
Carbaryl:
Carbaryl is a contact and stomach insecticide. It is most
popular insecticide because it is effective against a wide range of insects and
possesses very low mammalian toxicity. It is compatible with many pesticides
except Bordeaux mixture lime sulphur and urea. It is not effective against
mites.
Formulations:
WP 50%, Granule 4% and Dusts 5%
Trade
names: Sevin.
LD50
value: 400 mg/kg
2.
Propoxur(Arprocarb)
It is a broad spectrum, contact and stomach poison with
good knock down properties. It is effective in controlling house hold pests
such as cockroaches, crickets, flies etc. It has long residual action.
Formulations:
20% EC, 50% WP
Trade
names: Baygon, Bla ttamen, Saphaer
LD50
value: 90-128 mg/kg
3.
Carbofuran.
It is a plant systemic broad spectrum and long residual
insecticide, miticide and nematicide. It is recommended as soil insecticides
against plant sap sucking and borer
pests.
Formulation: 3G,48F
Trade
names: Furadan
LD50
value: 8-14 mg/kg
4.
Carbosulfan.
It is
a systemic insecticide, and nematicide. It is recommended as seed dresser insecticide
Formulation:
25 DS
Trade
name: Marshal
5.
Thiodicarb
It is
a insecticide with ovicidal properties, and molluscicide.
Formulation:
75 WP
Trade
name: Larvin
6.
Aldicarb
It is systemic pesticide usually applied in soil as seed
furrow, band or broadcast treatments either pre-plant or at planting as well as
post emergence side dress treatments. It has also possessing acaricidal
property and toxic to higher animals. Insecticide of carbamate group which is highly
toxic to mammals.
Formulation:
10 G
Trade
names: Temik
LD50
value: 0.93 mg/kg
5. Methomyl:
It is a systemic with contact and stomach insecticide and
nematicide. It is very effective against a wide variety of pests particularly
army worms, cabbage semilooper, Okra stem fly, fruit borers, leaf defoliators,
cotton boll worms, etc. It is insecticide belonging to carbamate groups that
has ovicidal action against lepidopteran pests (Helicoverpa armigera).
Formulations:
90 WP,12.5 EC, 40 SP
Trade
names: Lannate, Dunnate
LD50
value: 30 mg/kg
SYNTHETIC
PYRETHROIDS AND INSECTICIDES OF OTHER GROUPS
Synthetic pyrethroids have got the properties of
plant derivative pyrethrum as insecticides but areconsiderably more stable in
light and air. Allethrin was first synthetic analogue of pyrethroids.
They act on tiny channel through which sodium is pumped to
cause excitation of neurons and prevent the sodium channels from
closing,resulting in continual nerve trans mission, tremors and eventually
death.
The synthetic pyrethroids have extremely high insecticidal
activity at extremely low doses and are bio-degradable in nature. Their
activity is most pronounced against lepidopterous pests and they are very
effective against beetle, leaf miner and bugs. They are very effective against
eggs, larval and adult stages of insects. They have antifeedant and repellent
properties. They are not readily washed off from the plants by rain due to
lipophilic characters.
These synthetic pyrethroids are very less toxic to mammals
and having a quick knock down activity to insects, the lower toxicity to
mammals and increase safety for the
user.Very low application rate of synthetic pyrethroids as compared to conventional
insecticides brings reduced
environmental pollution.
Limitations
- A major limitation of synthetic pyrethroids is that these are generally not effective as soil insecticide.
- Even at low dosages kill non target species.
- Synthetic pyrethroids cause resurgence of several groups of insect pests especially whiteflies and aphids.
- Rapid development of resistance to synthetic pyrethroids in many insect species. This may be due to high selection pressure exerted by high mortality caused by synthetic pyrethroids
- Synthetic pyrethroids are poor acaricides
First generation: First generation pyrethroids are
considered to be of low toxicity to people and other mammals because they are
rapidly broken down in the body. First generation pyrethroids decompose quickly
in sunlight and air and thus pose little risk in the environment but all
pyrethroids are toxic to aquatic animals.
1)
Allethrin
It is contact, stomach and respiratory action and bring
quick knock down of flies and mosquitoes when applied in combina tion with
Piperonyl butoxide. These are lipophlic compounds. In 1949, the first synthetic
pyrethrum analougue allethrin commercially introduced.
Trade name: Pynamin
LD50 value: rats 572-1100 mg/Kg for rats and Dermal
LD50 >2000 mg/kg
Second generation: Second generation pyrethroids
are not acutely toxic to people or other mammals.These pyrethroids decompose
rapidly in sunlight. They thus pose little threat to the environment, but for
the same reason they are not suitable for agricultural use.
2) Resmethrin
. Approximately 20 times more effective than pyrethrum in
housefly knock down, and is not synergized to any appreciable extent with pyrethrum
synergists.
Trade name: NRDC – 104, SBP-1382, and FMC – 17370
LD50 value Dermal LD50 2000-3000 mg/kg
3) Bioresmethrin
It is stereoisomer of resmethrin. Appeared in 1967.50
times more effective than pyrethrum against normal (susceptible to insects)
houseflies, and also not synergized with pyrethrum synergists. Both resmethrin
& Bioresmethrin decompose fairly rapidly on exposure to air & sunlight,
so never developed for agricultural use.
Trade name: NRDC-107,FMC –18739, and RU-1148
LD50: 8,600 mg/kg (oral) and 10,000 mg/kg (dermal).
4) Bioallethrin
(d-trans –allethrin) introduced in 1969. More potent than
allethrin
and readily synergized, but it is not as effective as resmethrin.
Third generation: Third generation pyrethroids do
not decompose in sunlight and contain some of the most powerful insecticides
known. Third generation pyrethoids are not highly toxic to people or other
mammals mainly because they decompose rapidly in the body.
5)
Fenvalerate:
It is
contact insecticide and of broad spectrum in nature. It is stable in sunlight
and has longer residual toxicity.
Formulations:
20 EC
Trade
names: Fenvel, Bilfen, Belmark, Sumicidin, Pydrin
LD50
value: 300-630 mg/kg
6) Permethrin:
Contact insecticide, light stable, but poor knock down.
First agricultural pyrethroidsbecause of their exceptional insecticidal
activity (0.11 kg a.i/ha) and their photo stability.
Formulations:
25 EC and 5% smoke generation
Trade
names: Ambush , pounce , pramex
LD50
value: Acute oral LD50 : 7000 mg/kg, Dermal LD50: >5100 mg/kg
119
Fourth generation: Offer the most resistance to
exposure to sunlight and air and, therefore, are more persistent. This group is
more toxic to people than other pyrethroids and therefore requires more care in
use. More stable in the environment.
7) Cyhalothrin
Non-systemic insecticide with contact and stomach action,
and repellent properties.gives rapid knockdown and long residual activity. It
is an insecticide and acaricide used to control
a wide range of pests.
Formulations: 2.5 EC, 5% EC
Trade names: Kung-Fu,Reeva, Charge, Excaliber, Grenade,
Hallmark, Karate,
Matador, Samurai and Sentinel.
LD50
value: 56 mg/kg
8)
Cyfluthrin
It is a non-systemic contact and stomach poison,with rapid
knock down effect. It is for control of chewing and sucking insects on crops.
Cyfluthrin is also used in public health situations and for structural pest
control.
Formulations:
5 EC, 10% EC
Trade
names: Contur, Laser, Responsar, Tempo
LD50
value: 869 - 1271 mg/kg
9)
Cypermethrin
It is
stomach and contact insecticide. It is very effective against different types
of pests on various crops.
Formulations:
10 EC, 25 EC
Trade
names: Cyper guard, Ripcord, Cymbush and Cyper kill
LD50
value: ha Oral LD50 303-4123 MG /KG, dermal more than 2400mg/kg
10)
Fenpropathrin
It is contact insecticide and of broad spectrum in
nature.It is extremely toxic to fish, wildlife.and aquatic organisms. It have
acaricidal and miticidal property.
Formulations:
2.4 EC, 10 or 20% EC.
Trade
names: Danitol, Rody and Meothrin
LD50
value:54 mg/kg
11)
Flucythrinate
Flucythrinate is a synthetic pyrethroid used to control
insect pests in apples, cabbage, field corn, head lettuce and pears, and to
control Heliothis spp. in cotton.
Trade
names: AASTAR, AC 222705, Cybolt, Fuching Jujr, OMS 2007, and Pay-Off.
LD50 value: 81 mg/kg .dermal LD50 in rabbits of
greater than 1000 mg/kg
12)
Decamethrin (Deltamethrin)
It is more potent than any other insecticide. It has also
proved effective even against insects resistant to conventional insecticides.It
is contact and stomach insecticide.
Formulations:
2.8 EC, 2.5% WP
Trade
names: Decis, Decaguard, Deltex
LD50
value:135mg/kg
13)
Fluvalinate
It is
a insecticide and acaricide with stomach and contact activity in target
insects. It
is
used as a broad spectrum insecticide.
Formulations:
25 EC
Trade
names: Klartan, Mavrik, Mavrik Aqua Flow, Spur and Yardex
LD50
value: 1,050 to 1,110 mg/kg
14)
Fenfluthrin: It is a very potent recent synthetic pyrethroid against a
various groups of insects and mites. Highly toxic to Daphnia (Aquatic Invertebrate)
Trade
Names: Bayticol, Bayvarol, Baynac
Comments
Post a Comment