Permethrin
- CAS No.
- 52645-53-1
- Chemical Name:
- Permethrin
- Synonyms
- permethrine;Nix;permetrin;Permetrina;kudos;SPARTAN;Permethrim;-1-carboxylate;DRAGON;Elimite
- CBNumber:
- CB8312237
- Molecular Formula:
- C21H20Cl2O3
- Molecular Weight:
- 391.29
- MDL Number:
- MFCD00041809
- MOL File:
- 52645-53-1.mol
- MSDS File:
- SDS
- TDS File:
- TDS
| Melting point | 34-35°C |
|---|---|
| Boiling point | bp0.05 220° |
| Density | 1.19 |
| vapor pressure | 7×10-5 Pa (20 °C) |
| refractive index | 1.6500 (estimate) |
| Flash point | 10 °C |
| storage temp. | 0-6°C |
| solubility | DMF: 33 mg/ml; DMSO: 16 mg/ml; Ethanol: 14 mg/ml |
| form | Liquid |
| color | Light yellow to yellow |
| Water Solubility | insoluble |
| Merck | 13,7257 |
| BRN | 5765325 |
| Henry's Law Constant | 5.3×100 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) |
| Stability | Stable. Incompatible with strong oxidising agents. |
| Major Application |
agriculture environmental |
| Cosmetics Ingredients Functions | ANTIMICROBIAL |
| InChI | 1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3 |
| InChIKey | RLLPVAHGXHCWKJ-UHFFFAOYSA-N |
| SMILES | CC1(C)C(\C=C(/Cl)Cl)C1C(=O)OCc2cccc(Oc3ccccc3)c2 |
| LogP | 6.500 |
| CAS DataBase Reference | 52645-53-1(CAS DataBase Reference) |
| EWG's Food Scores | 4-5 |
| FDA UNII | 509F88P9SZ |
| ATC code | P03AC04,P03AC54 |
| NIST Chemistry Reference | Permethrin(52645-53-1) |
| IARC | 3 (Vol. 53) 1991 |
| Pesticides Freedom of Information Act (FOIA) | Permethrin |
| EPA Substance Registry System | Permethrin (52645-53-1) |
| UNSPSC Code | 41116107 |
| NACRES | NA.24 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |   GHS07,GHS09 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H302+H332-H317-H410 | |||||||||
| Precautionary statements | P261-P273-P280-P301+P312-P302+P352-P304+P340+P312 | |||||||||
| PPE | dust mask type N95 (US), Eyeshields, Faceshields, Gloves | |||||||||
| Hazard Codes | Xn,N,T,F | |||||||||
| Risk Statements | 20/22-43-50/53-39/23/24/25-23/24/25-11-51/53-36-20/21/22 | |||||||||
| Safety Statements | 13-24-36/37/39-60-61-45-36/37-16-7-26 | |||||||||
| RIDADR | UN1230 3/PG 2 | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | GZ1255000 | |||||||||
| HS Code | 29162090 | |||||||||
| Storage Class | 11 - Combustible Solids | |||||||||
| Hazard Classifications | Acute Tox. 4 Inhalation Acute Tox. 4 Oral Aquatic Acute 1 Aquatic Chronic 1 Skin Sens. 1 |
|||||||||
| Hazardous Substances Data | 52645-53-1(Hazardous Substances Data) | |||||||||
| Toxicity | LD50 orally in female rats: 3801 mg/kg (Metker); LD50 in 8 day old rats, male adult rats (mg/kg): 340.5, 1500.0 orally (Cantalamessa) | |||||||||
| NFPA 704 |
|
Permethrin price More Price(53)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | Y0001741 | Permethrin for system suitability European Pharmacopoeia (EP) Reference Standard | 52645-53-1 | 100 mg | $167 | 2026-04-30 | Buy |
| Sigma-Aldrich | Y0001733 | Permethrin (25:75) European Pharmacopoeia (EP) Reference Standard | 52645-53-1 | 350 mg | $254 | 2026-04-30 | Buy |
| Sigma-Aldrich | 68216 | Permethrin certified reference material, TraceCERT®, mixture of cis and trans isomers, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland | 52645-53-1 | 100 mg | $158 | 2026-04-30 | Buy |
| Sigma-Aldrich | 45614 | Permethrin mixture of cis and trans isomers | 52645-53-1 | 250mg | $58.2 | 2026-04-30 | Buy |
| Sigma-Aldrich | Y0001741 | Permethrin for system suitability European Pharmacopoeia (EP) Reference Standard | 52645-53-1 | 60 mg | $156 | 2025-07-31 | Buy |
Permethrin Chemical Properties,Uses,Production
Description
Yellow-brown to brown liquid, which sometimes tends to crystallize at room temperature (technical grade).
Permethrin, a pyrethroid insecticide with little mammalian toxicity, has been marketed as a tick repellent. Permethrin is the only synthetic pyrethroid that is used worldwide for head lice. The spray formulation is the most widely available form. Once applied to clothing, it is stable through several wash cycles. It is also suitable for treating sleeping bags, tents, and fabric used for insect screening. A liquid concentrate has been used to impregnate fabric for as long as the life of the garment. Permethrin is particularly helpful in the prevention of tick and chigger bites. These crawling arthropods must travel across the treated fabric, whereas flying insects tend to be attracted directly to exposed skin. The combination of a DEET-containing repellent and permethrin-treated clothing is generally highly ffective against a wide range of biting arthropods.
Chemical Properties
Crystalline Solid
Uses
Permethrin is a synthetic pyrethroid active against lice, ticks, mites, and fleas. It acts on neural cellmembranes, delaying repolarization and causing paralysis. The compound has no reported adverse properties, is heat and light stable, has 70% to 80% ovicidal activity, and leaves an active residue on the scalp. Permethrin is 26 times less toxic than lindane and 3 times less toxic than pyrethrins. A 1% permethrin cream rinse (Nix) preparation with a single application was determined to be more effective than treatment with RID. Permethrin-treated military uniforms are effective against human body lice. Apply the cream rinse for 10 minutes and rinse off with water. Localized pruritus may be reported with use of this product.
Uses
Labelled Permethrin (P288500). Synthetic pyrethroid insectide, more stable to light and at least as active as the natural pyrethrins and with low mammalian toxicity.
Uses
For the treatment of infestation with Sarcoptes scabiei (scabies); antihyperlipidemic; cholesterol sequestrant.
Definition
ChEBI: 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.
Indications
Permethrin is a synthetic pyrethroid active against lice, ticks, mites, and fleas. It
acts on neural cellmembranes, delaying repolarization and causing paralysis. The
compound has no reported adverse properties, is heat and light stable, has 70%
to 80% ovicidal activity, and leaves an active residue on the scalp.
Permethrin 0.5% spray kills ticks and repels mosquitoes and stable flies. It is broken
down when applied to skin and, hence, should be applied to clothing, shoes, tents,
and so on. Spray only enough to moisten the material. Spray on clothing at least 2
hours before wearing. One treatment should last through a few washings.
Production Methods
The production of permethrin involves a multi-step chemical synthesis starting with 1,1-dichloro-4-methyl-1,3-pentadiene, which reacts with ethyl diazoacetate in the presence of a copper catalyst to form a cyclopropane intermediate: ethyl (±)-cis,trans-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropane carboxylate. This intermediate is then hydrolysed to yield the corresponding carboxylic acid, which contains both cis- and trans-isomers. To separate these, the mixture is treated with n-hexane, where the cis-isomer dissolves and the trans-isomer precipitates. The trans-isomer is then filtered and esterified with 3-phenoxybenzyl alcohol, producing permethrin as the final product.
brand name
Elimite (Allergan); Nix (GlaxoSmithKline).
General Description
Pale brown liquid. Relatively water insoluble. Used as an insecticide.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
A pyrethroid derivative.
Contact allergens
Pyrethroids, also called pyrethrinoids, are neurotoxic synthetic compounds used as insecticides, with irritant properties. Cypermethrin and fenvalerate have been reported as causing positive allergic patch tests, but only fenvalerate was relevant in an agricultural worker.
Mechanism of action
Broad-spectrum with contact and stomach action. Slight repellant effect. Sodium channel modulator.
Pharmacology
Permethrin is a synthetic pyrethroid that interferes with the influx of sodium through cell membranes, leading to neurologic paralysis and death of the mite. There is minimal percutaneous absorption (<2%), which is rapidly hydrolyzed and excreted in the urine. Permethrin 5% dermal cream (Elimite) is applied for 8 to 12 hours to the entire body from the chin down and is then washed off.
Clinical Use
Permethrin is 3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarboxylicacid (3-phenoxyphenyl)methylester or 3-(phenoxyphenyl)methyl (±)-cis, trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate(Nix). This synthetic pyrethrinoid compound is more stablechemically than most natural pyrethrins and is at least as activeas an insecticide. Of the four isomers present, the1(R),trans and 1(R),cis-isomers are primarily responsiblefor the insecticidal activity. The commercial product is amixture consisting of 60% trans and 40% cis racemic isomers.It occurs as colorless to pale yellow low-melting crystalsor as a pale yellow liquid and is insoluble in water butsoluble in most organic solvents.
Permethrin exerts a lethal action against lice, ticks, mites,and fleas. It acts on the nerve cell membranes of the parasitesto disrupt sodium channel conductance. It is used as apediculicide for the treatment of head lice. A single applicationof a 1% solution effects cures in more than 99% ofcases. The most frequent side effect is pruritus, which occurredin about 6% of the patients tested.
Safety Profile
Poison by inhalation, intravenous, and intracerebral routes. Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. A skin irritant. When heated to decomposition it emits toxic fumes of Cl-. See also ESTERS
Veterinary Drugs and Treatments
Permethrin is synthetic pyrethroid that acts as an adulticide insecticide/miticide. It has knockdown activity against fleas, lice, ticks, and
certain mites (e.g., Cheyletiella, Sarcoptes scabiei) and also has repellant activity. In small animal medicine, it is used primarily for fleas
and ticks on dogs. In large animal and food animal medicine, there are many products (not listed below) available for pour-on, dusting,
and spray use for flies, lice, mites, mosquitoes, ticks and keds.
Permethrin acts by disrupting the sodium channel current in arthropod nerve cell membranes, resulting in paralysis and death.
Environmental Fate
Soil. Permethrin biodegraded rapidly via hydrolysis yielding 3-(2,2-dichloroethenyl)-
2,2-dimethylcyclopropanecarboxylic acid and 3-phenoxybenzyl alcohol (Kaufman et al.,
1981). The reported half-life in soil containing 1.3–51.3% organic matter and pH 4.2–7.7
is <38 days (Worthing and Hance, 1991)
In lake water, permethrin degraded more rapidly than in flooded sediment to transand cis-(dichlorovinyl)dimethylcyclopropanecarboxylic acid. The cis isomer was more
stable toward biological and chemical degradation than the trans isomer (Sharom and
Solom
Plant. Metabolites identified in cotton leaves included trans-hydroxypermethrin, 2′-
hydroxypermethrin, 4′-hydroxypermethrin, dichlorovinyl acid, dichlorovinyl acid conjugates, hydroxydichlorovinyl acid, hydroxydichlorovinyl acid conjugates, phe
Dislodgable residues of permethrin on cotton leaves 0, 24, 48, 72 and 96 hours after
application (1.1 kg/ha) were (cis:trans): 0.26:0.38, 0.24:0.34, 0.22:0.32, 0.16:0.24 and
0.15:0.21 μg/m2, respectively (Buck et al., 1980).
Photolytic. Photolysis of permethrin in aqueous solutions containing various solvents
(acetone, hexane and methanol) under UV light (λ >290 nm) or on soil in sunlight initially
resulted in the isomerization of the cyclopropane moiety and ester cl
Metabolic pathway
Permethrin was one of the first photostable pyrethroids suitable for field
use.It served as a precursor for others such as its α-cyano analogue,
cypermethrin. As it lacks the cyano group it has no chirality at the acarbon
atom and therefore consists of a mixture of only four isomers. It is
hydrolysed more readily than cypermethrin because it is an ester of a
primary alcohol.
Much of the early research on the metabolism of the synthetic, photostable
pyrethroids was conducted by Casida and co-workers on permethrin.
The published results greatly assisted subsequent work on the
analogues. This is stressed because some of the information reported
below will draw on the metabolic schemes given in the cypermethrin
entry.
The environmental fate of permethrin and its metabolism in plants,
insects, animals and fish have been reported. The insecticide is metabolised
by ester cleavage to its constituent acid and alcohol and subsequent
conjugation of these. The primary metabolites are also subject to oxidation
prior to conjugation. Permethrin itself is also subject to oxidation, the cisisomers
more so than the trans-isomers because the former is more slowly
hy droly sed.
Degradation
Permethrin is stable as a solid but it is readily hydrolysed in solution under alkaline conditions; it is most stable at pH 4. It is relatively resistant to photodegradation in the context of field use but it undergoes facile photoisomerism (Holmstead et al., 1978). It can be degraded under laboratory conditions affording DCVA (2) and 3-phenoxybenzyl alcohol (3PBAlc, 3). Under appropriate conditions, trans-permethrin affords 29% trans-DCVA and 13% cis-DCVA. The mechanisms of these reactions have been reviewed in detail by Ruzo (1982). Permethrin is resistant to photo-oxidation; other reactions, such as dechlorination, are of minor importance. The degradation products are shown in Scheme 1.
Toxicity evaluation
Acute oral LD50 for rats: 430-4,000 mg/kg (cis:trans ca. 40:60); ca. 6,000 mg/kg (cis:trans ca. 20:80)
Pesticide Type
Insecticide; Veterinary substance
Permethrin Preparation Products And Raw materials
Raw materials
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Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Hubei Shiteng Chemical Technology Co. LTD | 19086915685 18971850150 | 1273131441@qq.com | China | 4993 | 58 |
| Wuhan Topule | +86-02787215551 19945035818 | 2936752263@qq.com | China | 7985 | 58 |
| Wuhan penglei Biotechnology Co., Ltd | 13554168242 | 445014292@qq.com | China | 281 | 58 |
| J & K SCIENTIFIC LTD. | 18210857532 18210857532 | jkinfo@jkchemical.com | China | 96815 | 76 |
| TAIYUAN RHF CO.,LTD. | +86 351 7031519 | sales@RHFChem.com | China | 2334 | 56 |
| ShangHai DEMO Chemical Co.,Ltd | 400-021-7337 2355568890 | sales@demochem.com | China | 2569 | 57 |
| Pure Chemistry Scientific Inc. | 001-857-928-2050 or 1-888-588-9418 | sales@chemreagents.com | United States | 10174 | 62 |
| Shanghai Hanhong Scientific Co.,Ltd. | 021-54306202 13764082696 | info@hanhongsci.com | China | 42917 | 64 |
| Chemsky（shanghai）International Co.,Ltd. | 021-50135380 | shchemsky@sina.com | China | 32273 | 50 |
| Sichuan Kulinan Technology Co., Ltd | 400-1166-196 18981987031 | cdhxsj@163.com | China | 11674 | 57 |
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View Lastest Price from Permethrin manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2026-09-12 | Permethrin
52645-53-1
|
0.99 | RongNa Biotechnology Co.,Ltd | ||||
 |
2026-09-11 | Permethrin
52645-53-1
|
25kg | 95%TC | 40tons/month | WUHAN FORTUNA CHEMICAL CO., LTD | ||
 |
2026-09-02 | Permethrin
52645-53-1
|
$1.00-6.00 | 1KG | 99% | Henan Fengda Chemical Co., Ltd |
-
- Permethrin
52645-53-1
- 0.99
- RongNa Biotechnology Co.,Ltd
-
- Permethrin
52645-53-1
- 95%TC
- WUHAN FORTUNA CHEMICAL CO., LTD
-
- Permethrin
52645-53-1
- $1.00-6.00
- 99%
- Henan Fengda Chemical Co., Ltd
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