CAS Number: 52645-53-1
Formula: C21H20Cl2O3
Molar mass: 391.29 g·mol−1
Permethrin
APPLICATIONS
Permethrin, a pyrethroid, is active against a broad range of pests including lice, ticks, fleas, mites, and other arthropods.
Further, Permethrin is an insecticide in the pyrethroid family.
Permethrin is a synthetic chemical that acts like a natural extract from thflower.
Moreover, Permethrin is used in a number of ways to control insects.
Products containing permethrin may be used in public health mosprograms.
They may be used on food and feed crops, on ornamental lawns, on livestock and pets, in structures and buildings, and on clo
Permethrin may also be used in places where food is handled, such as restaurants.
More to that, Permethrin was first registered with the United States Environmental Protection Agency (U.S. EPA) in 1979, and was re-registe
Permethrin is used as an ectoparasiticide in humans and animals.
Furthermore, Permethrin is used as a nematocide, acaricide, and insecticide.
Permethrin is registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses.
The pyrethroids are the most widely used class of insecticides in wood preservation because of their broad-spectrum activity, high efficacy especially against wood boring beetle, and high resistance to leaching.
Permethrin has a potential application for forest protection and vector control for the control of noxious insects in the household and on cattle, for the control of body lice, and in mosquito nets.
Permethrin is used to treat head lice, tiny insects that infest and irritate your scalp.
Further, Permethrin is also used to help avoid infestation in people who have close contact with someone who has head lice.
Permethrin belongs to a class of drugs known as pyrethrins.
Moreover, Permethrin works by paralyzing and killing lice and their eggs (nits).
Permethrin may also be used for pubic lice.
Permethrin is available under the following different brand names: Nix, Elimite, and Acticin.
Dosage Considerations – Should be Given as Follows:
Scabies
Cream:
Apply from head to toe, leave on for 8-14 hours, rinse; may reapply in 7 days if live mites reappear.
The single application is usually curative.
Head Lice and Nits (Eggs)
Lotion/cream rinse/liquid:
Apply to washed hair, leave on 10 minutes, rinse and comb out nits and eggs; may repeat in 7 days if lice or nits still present.
The single application is usually curative.
Uses of Permethrin:
Insecticide:
In agriculture, to protect crops (a drawback is that it is lethal to bees)
In agriculture, to kill livestock parasites
For industrial and domestic insect control
In the textile industry, to prevent insect attack of woollen products
In aviation, the WHO, IHR and ICAO require arriving aircraft be disinsected prior to embarkation, departure, descent, or deplaning in certain countries. Aircraft disinsection with permethrin-based products is recommended only prior to embarkation.
Prior to departure (after boarding), at the top of descent or on arrival, d-phenothrin-based (1R-trans phenothrin) aircraft insecticides are recommended.
Insect repellent:
As a personal protective measure, permethrin is applied to clothing.
Permethrin is a cloth impregnant, notably in mosquito nets and field wear.
Note that while permethrin may be marketed as an insect repellent, it doesn't prevent insects from landing.
Instead Permethrin works by incapacitating or killing insects before they can bite.
In pet flea preventive collars or treatment (safe for use on dogs but not cats)
In timber treatment:
Pest control / effectiveness and persistence:
In agriculture, permethrin is mainly used on cotton, wheat, maize, and alfalfa crops.
Its use is controversial because, as a broad-spectrum chemical, Permethrin kills indiscriminately; as well as the intended pests, it can harm beneficialinsects, including honey bees, as well as cats and aquatic life.
Permethrin kills ticks and mosquitoes on contact with treated clothing.
A method of reducing deer tick populations by treating rodent vectors involves stuffing biodegradable cardboard tubes with permethrin-treated cotton.
Mice collect the cotton for lining their nests.
Permethrin on the cotton instantly kills any immature ticks feeding on the mice.
Permethrin is used in tropical areas to prevent mosquito-borne disease such as dengue fever and malaria.
Mosquito nets used to cover beds may be treated with a solution of permethrin.
This increases the effectiveness of the bed net by killing parasitic insects before they are able to find gaps or holes in the net.
Personnel working in malaria-endemic areas may be instructed to treat their clothing with permethrin as well.
Permethrin is the most commonly used insecticide worldwide for the protection of wool from keratinophagous insects such as Tineolabisselliella.
Permethrin affects the neuronal membrane by blocking the movement of sodium ions from outside to inside the neuronal cell membrane thereby disrupting the sodium channel current that regulates the polarization of the membrane.
This leads to delayed repolarization and subsequent paralysis of the nervous system.
Permethrin is used to eradicate parasites such as head lice, ticks and scabies from humans and animals.
Medical use of Permethrin:
Permethrin is available for topical use as a cream or lotion.
It is indicated for the treatment and prevention in exposed individuals of head lice and treatment of scabies.
Permethrin has an excellent safety profile; its main drawback is its cost.
For treatment of scabies:
Adults and children older than 2 months are instructed to apply the cream to the entire body from head to the soles of the feet.
Wash off the cream after 8–14 hours.
In general, one treatment is curative.
A single application of permethrin is more effective than a single oral dose of ivermectin for scabies.
In addition permethrin provides more rapid symptomatic relief than ivermectin.
When a second dose of ivermectin is days later, the efficacy between permethrin and ivermectin approach parity.
For treatment of head lice:
Apply to hair, scalp, and neck after shampooing.
Leave in for 10 minutes and rinse.
Avoid contact with eyes.
Permethrin is used in tropical areas to prevent mosquito-borne disease such as dengue fever and malaria.
Mosquito nets used to cover beds may be treated with a solution of permethrin.
This increases the effectiveness of the bed net by killing parasitic insects before they are able to find gaps or holes in the net. Personnel working in malaria-endemic areas may be instructed to treat their clothing with permethrin as well.
Permethrin is the most commonly used insecticide worldwide for the protection of wool from keratinophagous insects such as Tineola bisselliella.
To better protect soldiers from the risk and annoyance of biting insects, the British and US armies are treating all new uniforms with permethrin.
Permethrin (as well as other long-term pyrethroids) is effective over several months, in particular when used indoors.
International studies report that permethrin can be detected in house dust, in fine dust, and on indoor surfaces even years after the application.
The degradation rate of Permethrin under indoor conditions is approximately 10% after 3 months.
Resistance:
Contrary to the most common mechanism of insecticide resistance evolution – selection for preexisting, low-frequency alleles – in Aedes aegypti permethrin resistance has arisen through the mechanism common to pyrethroids and DDT known as "knockdown resistance" (kdr) mutations.
While Permethrin is manmade, it resembles naturally occurring chemicals called pyrethroids that are naturally found in chrysanthemums, which haveinsecticidal properties.
Permethrin kills many different types of insects by paralyzing the nervous system.
Permethrin works when ingested or through direct contact and kills adults, eggs, and larvae.
Further, Permethrin lasts up to 12 weeks post application.
DESCRIPTION
Permethrin is a synthetic broad-spectrum insecticide classified as one of the oldest organic insecticides.
Furthermore, Permethrin is a pyrethroid insecticide commonly used in the treatment of lice infestations and scabies.
Permethrin is an insecticide used to prevent infestation with Sarcoptes scabiei (scabies).
Permethrin is a medication and an insecticide.
As a medication, Permethrin is used to treat scabies and lice.
Permethrin is applied to the skin as a cream or lotion.
As an insecticide, Permethrin can be sprayed onto clothing or mosquito nets to kill the insects that touch them.
Side effects of Permethrin include rash and irritation at the area of use.
Use of Permethrin during pregnancy appears to be safe.
Permethrin is approved for use on and around people over the age of two months.
Permethrin is in the pyrethroid family of medications.
Further, Permethrin works by disrupting the function of the neurons of lice and scabies mites
Permethrin was discovered in 1973.
Permethrin is on the World Health Organization's List of Essential Medicines.
In 2020, Permethrin was the 427th most commonly prescribed medication in the United States, with more than 100 thousand prescriptions.
Permethrin is a widely-used pesticide of the pyrethroid family.
Permethrin interacts with voltage-gated Na+ channels and inhibits their natural deactivation, causing the channels to remain open for a long time and destroying equilibrium of the neuronal system.
More specifically, Permethrin is known to delay channel deactivation of the NaV1.8 channel expressed in X.
Pyrethroids such as Permethrin are also thought to interact with GABA receptors and associated pathways.
Compared to mammalian sodium channels, Permethrin is at least 100 times more potent against insect sodium channels.
This medication is used to treat scabies, a condition caused by tiny insects called mites that infest and irritate your skin.
Permethrin belongs to a class of drugs known as pyrethrins.
Furthermore, Permethrin works by paralyzing and killing the mites and their eggs.
Permethrin is a pale brown liquid.
Moreover, Permethrin is relatively water insoluble.
Permethrin is used as an insecticide.
Permethrin is a synthetic pyrethroid and neurotoxin.
Permethrin affects the neuronal membrane by blocking the movement of sodium ions from outside to inside the neuronal cell membrane thereby disrupting the sodium channel current that regulates the polarization of the membrane.
This leads to delayed repolarization and subsequent paralysis of the nervous system.
Permethrin is used to eradicate parasites such as head lice, ticks and scabies from humans and animals.
Permethrin is a cyclopropanecarboxylate ester in which the esterifying alcohol is 3-phenoxybenzyl alcohol and the cyclopropane ring is substituted with a 2,2-dichlorovinyl group and with gem-dimethyl groups.
Permethrin has a role as a pyrethroid ester insecticide, a pyrethroid ester acaricide, an agrochemical, an ectoparasiticide and a scabicide.
More to that, Permethrin is a member of cyclopropanes and a cyclopropanecarboxylate ester.
Permethrin is functionally related to a 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid.
PROPERTIES
Molecular Weight: 391.3
XLogP3: 6.5
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 7
Exact Mass: 390.0789499
Monoisotopic Mass: 390.0789499
Topological Polar Surface Area: 35.5 Ų
Heavy Atom Count: 26
Formal Charge: 0
Complexity: 521
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 2
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Density: 1.19 g/cm3, solid g/cm3
Melting point: 34 °C (93 °F)
Boiling point: 200 °C (392 °F)
FIRST AID
Description of first aid measures:
General information:
Symptoms of poisoning may even occur after several hours; therefore medical observation for at least 48 hours after the accident.
After inhalation:
Supply fresh air and to be sure call for a doctor.
In case of unconsciousness place patient stably in side position for transportation.
After skin contact:
Immediately wash with water and soap and rinse thoroughly.
After eye contact:
Rinse opened eye for several minutes under running water.
After swallowing:
Immediately call a doctor.
Information for doctor:
Most important symptoms and effects, both acute and delayed:
May cause anemia, cough, CNS depression, drowsiness, headache, heart damage, lassitude
(weakness, exhaustion), liver damage, narcosis, reproductive effects, teratogenic effects.
No further relevant information available.
Indication of any immediate medical attention and special treatment needed:
No further relevant information available
HANDLING AND STORAGE
Handling
Precautions for safe handling:
Thorough dedusting.
Ensure good ventilation/exhaustion at the workplace.
Information about protection against explosions and fires:
No special measures required.
Conditions for safe storage, including any incompatibilities
Storage:
Requirements to be met by storerooms and receptacles:
No special requirements.
Information about storage in one common storage facility:
Not required.
Further information about storage conditions:
Keep receptacle tightly sealed.
Specific end use(s):
No further relevant information available.
SYNONYMS
Permethrin
52645-53-1
Ambush
Transpermethrin
Pounce
Elimite
Imperator
NRDC-143
(3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate
UNII-509F88P9SZ
Hemoglobin atlanta-coventry
(+)-trans-Permethrin
Permethrine
Permetrina
Acticin
Ambushfog
Corsair
Dragnet
Ectiban
Kaleait
Kestrel
Outflank
Perigen
Permasect
Perthrine
Stomoxin
Stomozan
Coopex
Eksmin
Picket
Expar
Kafil
Kavil
Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester
Anomethrin N
Ridect pour-on
CHEBI:34911
509F88P9SZ
1RS cis-Permethrin
52341-32-9
1RS,cis-Permethrin
NCGC00159390-02
1RS-trans-Permethrin
Kudos
Transpermethrin [ISO]
(+-)-cis-Permethrin
DSSTox_CID_2292
3-phenoxybenzyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
trans-(+-)-Permethrin
DSSTox_RID_76537
DSSTox_GSID_22292
3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropane carboxylic acid, (3-phenoxyphenyl) methyl ester
Permethrinum
S-3151
Chinetrin
Ecsumin
Efmethrin
Indothrin
Lyclear
NRDC 146
NRDC 148
Quamlin
Stomoxi
Cosair
Exmin
Exsmin
Ipitox
SBP-1513
(+-)-trans-Permethrin
Permethrine,c&t
(+-)-cis-Fmc 33297
Diffusil H
Insorbcid MP
Stomoxin P
Outflank-stockade
Perigen W
Dragnet FT
Picket G
Permethrin,racemic
[3-(phenyloxy)phenyl]methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
Mitin BC
Permanone 80
Permasect-25EC
FMC 35171
93389-07-2
SMR000778043
Kestrel (pesticide)
LE 79-519
Antiborer 3768
CAS-52645-53-1
Bematin 987
NRDC 143
Permethrinum [Latin]
Permetrin (Hungarian)
Permitrene (Hungarian)
Permetrina [Portuguese]
HSDB 6790
m-Phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
BW-21-Z
S 3151
Cyclopropanecarboxylic acid, 3-(2,2-dichlorovinyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester, (1R-trans)-
OMS 1821
Hb Atlanta-coventry
EINECS 258-067-9
Elimite (TN)
FMC 41655
Hb At-Co
EPA Pesticide Chemical Code 109701
JF 7065
BRN 2063148
WL 43479
AI3-29158
Permethrin (USAN/INN)
CHEMBL1525
SCHEMBL26543
Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester, cis-(+-)-
Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester, trans-(+-)-
MLS001332525
MLS001332526
Permethrin [ANSI:BSI:ISO]
Permethrin cis/trans ~ 1:1
Permethrin, analytical standard
DTXSID8022292
SCHEMBL15218274
HMS2232L22
HMS3264N07
HMS3369D10
Pharmakon1600-01504932
Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester, (1R,3S)-rel-
Cyclopropanecarboxylic acid, 3-(2,2-dichlorovinyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester, (1R-cis)-
HY-B0887
3-Phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
3-Phenoxybenzyl(+-)-cis, trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate
m-Phenoxybenzyl (+-)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
m-Phenoxybenzyl (+1)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
Permethrin 10 microg/mL in Cyclohexane
Permethrin 100 microg/mL in Cyclohexane
(3-Phenoxyphenyl)methyl (+-)-cis,trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
3-(Phenoxyphenyl)methyl (+-)-cis,trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
52341-33-0
Permethrin (isomers), analytical standard
DB-052153
Total Permethrin 100 microg/mL in Acetone
Permethrin, PESTANAL(R), analytical standard
D05443
AB00918441_05
645P531
Q411635
J-523915
Permethrin (25:75), EuropePharmacopoeia (EP) Reference Standard
(1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclo-propanecarboxylate
3-phenoxybenzyl 2-(2,2-dichlorovinyl)3,3-dimethylcyclopropanecarboxylate
3-Phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
(3-phenoxyphenyl)methyl 3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropanecarboxylate
(3-phenoxyphenyl)methyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxyl ate
3-phenoxybenzyl (1RS)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
m-phenoxybenzyl 2,2-dimethyl-3-(2',2'-dichlorovinyl)-cyclopropanecarboxylate
Permethrin for system suitability, EuropePharmacopoeia (EP) Reference Standard
(3-Phenoxyphenyl)methyl (+-)cis,trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
(3-Phenoxyphenyl)methyl (+/-)-cis,trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
Cyclopropanecarboxylic acid, 3-(2,2-dichlorovinyl)-2,2-dimethyl-, 3-phenoxybenzyl ester, (+-)-, (cis,trans)-
Tox21_111627
Tox21_201586
Tox21_300691
(CIS+TRANS)-3-PHENOXYBENZYL 3-(2,2-DICHLOROETHENYL)-2,2-DIMETHYLCYCLOPROPANECARBOXYLATE
3-phenoxybenzyl (1RS)-cis,trans-3-(2,2-dichlorovinyl)- 2,2-dimethylcyclopropanecarboxylate
3-phenoxybenzyl (1RS)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
3-phenoxybenzyl (1RS)-cis-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
[3-(phenoxy)phenyl]methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate
[3-(phenyloxy)phenyl]methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate
Cyclopropanecarboxylic acid *3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methylester
m-phenoxybenzyl (1RS,3RS,1SR,3SR-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
m-Phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
m-phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
Permethrin
permethrin
permethrin (ISO
permethrin (ISO)
(1RS)-cis,trans-3-(2,2-dichlorowinylo)-2,2-dimetylocyklopropanokarboksylan 3-fenoksybenzylu (pl)
(1RS,3RS;1RS,3RS)-3-(2,2-dichlorowinylo)-2,2-dimetylocyklopropanokarboksylan 3-fenoksybenzylu (permetryna) (pl)
(1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-diméthylcyclopropanecarboxylate de 3-phénoxybenzyle (perméthrine) (fr)
(1RS,3RS;1RS,3SR)-3-(2,2-Diclorovinil)-2,2-dimetilciclopropanocarboxilato de 3-fenoxibencilo (permetrina) (es)
(1RS,3RS;1RS,3SR)-3-(2,2-diclorovinil)-2,2-dimetilciclopropanocarboxilato de 3-fenoxibenzilo (permetrina) (pt)
(1RS,3RS;1RS,3SR)-3-(2,2-διχλωροβινυλο)-2,2-διμεθυλοκυκλοπροπανοκαρβοξυλικό 3-φαινοξυβενζύλιο (Permethrin/Περμεθρίνη) (el)
(3-fenoxybenzyl)-3-(2,2-dichlóretenyl)-2,2-dimetylcyklopropánkarboxylát (permetrín) (sk)
3-(2,2-diclorovinil)-2,2-dimetilciclopropancarbossilato di m-fenossibenzile (it)
3-(2,2-diclorovinil)-2,2-dimetilciclopropanocarboxilato de m-fenoxibencilo (es)
3-(2,2-diclorovinil)-2,2-dimetilciclopropanocarboxilato de m-fenoxibenzilo (pt)
3-(2,2-διχλωροβινυλ)-2,2-διμεθυλκυκλοπροπανιοκαρβοξυλικό m-φαινοξυβενζύλιο (el)
3-fenoksibentsyyli-(1RS, 3RS; 1RS, 3SR)-3-(2,2-dikloorivinyyli)-2,2-dimetyylisyklopropaanikarboksylaatti (permetriini) (fi)
3-fenoksibenzil (1RS,3RS;1RS,3SR)-3-(2,2-dichlorvinil)-2,2-dimetilciklopropankarboksilatas (permetrinas) (lt)
3-fenoksibenzil (1RS,3RS;1RS,3SR)-3-(2,2-diklorovinil)-2,2-dimetilciklopropankarboksilat (permetrin) (sl)
3-fenoksibenzil 3-(2,2-diklorovinil)-2,2-dimetilciklopropankarboksilat (sl)
3-Fenoksibenzil(1RS,3RS;1RS,3SR)-3-(2,2-dihlorvinil)-2,2-dimetilciklopropānkarboksilāts (permetrīns) (lv)
3-fenoksübensüül-(1RS,3RS;1RS,3SR)-3-(2,2-diklorovinüül)-2,2-dimetüültsüklopropaankarboksülaat (permetriin) (et)
3-fenossibenzil-(1RS)-cis,trans-3-(2,2-diclorovinile)-2,2 dimetilciclopropano carbossilato (Permetrina) (it)
3-fenoxibensyl-(1RS,3RS;1RS,3SR)-3-(2,2-diklorovinyl)-2,2-dimetylcyklopropankarboxylat (Permetrin) (sv)
3-fenoxibenzil (1RS,3RS;1RS,3SR)-3-(2,2-diclorovinil)-2,2-dimetilciclopropancarboxilat (Permetrin) (ro)
3-fenoxibenzil (1RS,3RS;1RS,3SR)-3-(2,2-diklórvinil)-2,2-dimetil-ciklopropán-karboxilát (Permetrin) (hu)
3-fenoxibenzyl-3-(2,2-diklorvinyl-2-dimetylcyklopropankarbamatoxilat (sv)
3-Fenoxybenzyl(1RS,3RS;1RS,3SR)-3-(2,2-dichloorvinyl)-2,2-dimethylcyclopropaancarboxylaat (permethrin) (nl)
3-fenoxybenzyl(1RS,3RS;1RS,3SR)-3-(2,2-dichlorvinyl)-2,2-dimethylcyklopropankarboxylát (permethrin) (cs)
3-fenoxybenzyl-[3-(2,2-dichlorvinyl)-2,2-dimethylcyklopropan-1-karboxylát] (cs)
3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (Permethrin) (no)
3-Phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorvinyl)-2,2-dimethylcyclopropancarboxylat (Permethrin) (de)
3-phenoxybenzyl-(1RS,3RS;1RS,3SR)-3-(2,2-dichlorvinyl)-2,2-dimethylcyclopropancarboxylat (permethrin) (da)
3-феноксибензилов (1RS,3RS;1RS,3SR)-3-(2,2-дихлоровинил)-2,2-диметилциклопропанкарбоксилат (перметрин) (bg)
m-Fenoksibentsyyli-3-(2,2-dikloorivinyyli)-2,2-dimetyylisyklopropaanikarboksylaatti (fi)
m-fenoksibenzil 3-(2,2-diklorovinil)-2,2-dimetilciklopropankarboksilat (hr)
m-fenoksibenzil-3(2,2-dihlorvinil)-2,2-dimetilciklopropānkarboksilāts (lv)
m-fenoksibenzil-3-(2,2-dichlorvinil)-2,2-dimetilciklopropankarboksilatas (lt)
m-fenoksybenzyl-3-(2,2-diklorvinyl)-2,2-dimetylcyklopropankarboksylat (no)
m-fenoksübensüül-3-(2,2-diklorovinüül)-2,2- dimetüültsüklopropaankarboksülaat (et)
m-Fenossibenżil (1RS,3RS;1RS,3SR)-3-(2,2-diklorovinil)-2,2-dimetilċiklopropankarbossilat (Permetrin) (mt)
m-fenoxibenzil 3-(2,2-diclorovinil)-2,2-dimetilciclopropan-carboxilat (ro)
m-fenoxibenzil-3-(2,2-diklórvinil)-2,2-dimetilciklopropánkarboxilát (hu)
m-fenoxybenzyl-3-(2,2-dichloorvinyl)-2,2-dimethylcyclopropaancarboxylaat (nl)
m-phenoxybenzyl-3-(2,2-dichlorvinyl)-2,2-dimethylcyclopropancarboxylat (da)
m-Phenoxybenzyl-3-(2,2-dichlorvinyl)-2,2-dimethylcyclopropancarboxylat (de)
m-феноксибензил 3-(2,2-дихлоровинил)-2,2-диметилциклопропанкарбоксилат (bg)
O-(3-fenoxybenzyl)-3-(2,2-dichlórvinyl)-2,2-dimetylcyklopropánkarboxylát (sk)
permethrin (ISO) (cs)
permethrin (ISO) (da)
Permethrin (ISO) (de)
permethrin (ISO) (el)
permethrin (ISO) (nl)
permetriin (ISO) (et)
Permetrin (hr)
permetrin (no)
permetrin (ISO) (hr)
permetrin (ISO) (hu)
permetrin (ISO) (ro)
permetrin (ISO) (sl)
permetrin (ISO) (sv)
permetrina (ISO) (es)
permetrina (ISO) (pt)
permetrinas (ISO) (lt)
permetrine (ISO) (it)
permetryna (ISO) (pl)
permetrín (ISO) (sk)
permetrīns (ISO) (lv)
perméthrine (ISO) (fr)
perméthrine (ISO);3-(2,2-dichorovinyl)-2,2-diméthylcyclopropanecarboxylate de m-phénoxybenzyle (fr)
перметрин (ISO) (bg)
Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (3-phenoxyphenyl)methyl ester
