| Identification | More | [Name]
Permethrin | [CAS]
52645-53-1 | [Synonyms]
3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarboxylic acid (3-phenoxyphenyl)methyl ester
3-PHENOXYBENZYL (1RS)-CIS TRANS-3-(2,2-DICHLOROVINYL)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLATE
[3-PHENOXYPHENYL] METHYL-[+]-CIS-TRANS-3-[2,2-DICHLOROETHENYL]-2,2-DIMETHYLCYCLOPROPANE CARBOXYLATE
AMBUSH
ASSITHRIN
CLIPER
COOPEX
CORSAIR
DRAGNET
DRAGON
EKSMIN
KAFIL
m-Phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
PERMETHRIN
PERMETHRINE (CIS/TRANS)
(.+/-.)-3-Phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
(.+/-.)-m-Phenoxybenzyl-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-carboxylate
(+-)-,(cis,trans)-yleste
(3-phenoxyphenyl)methyl3-(2,2-dichlorethenyl)-2,2-dimethylcyclopropanecarbox
(3-Phenoxyphenyl)methyl-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate | [EINECS(EC#)]
258-067-9 | [Molecular Formula]
C21H20Cl2O3 | [MDL Number]
MFCD00041809 | [Molecular Weight]
391.29 | [MOL File]
52645-53-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Crystalline Solid | [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) | [Fp ]
10 °C | [storage temp. ]
0-6°C | [solubility ]
DMF: 33 mg/ml; DMSO: 16 mg/ml; Ethanol: 14 mg/ml | [form ]
neat | [color ]
Light yellow to yellow | [Stability:]
Stable. Incompatible with strong oxidising agents. | [Water Solubility ]
insoluble | [Usage]
Synthetic pyrethroid insectide, more stable to light and at least as active as the natural pyrethrins and with low mammalian toxicity | [Merck ]
13,7257 | [BRN ]
5765325 | [Henry's Law Constant]
5.3×100 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | [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 | [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. | [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) | [IARC]
3 (Vol. 53) 1991 | [NIST Chemistry Reference]
Permethrin(52645-53-1) | [EPA Substance Registry System]
52645-53-1(EPA Substance) |
| Hazard Information | Back Directory | [Chemical Properties]
Crystalline Solid | [Uses]
antihyperlipidemic, cholesterol sequestrant | [Uses]
For the treatment of infestation with Sarcoptes scabiei (scabies). | [Uses]
insecticide | [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. | [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. | [General Description]
Pale brown liquid. Relatively water insoluble. Used as an insecticide. | [Reactivity Profile]
A pyrethroid derivative. | [Air & Water Reactions]
Insoluble in water. | [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.
| [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). | [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. | [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 |
| Safety Data | Back Directory | [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 | [Hazard Codes ]
Xn,N,T,F | [Risk Statements ]
R20/22:Harmful by inhalation and if swallowed .
R43:May cause sensitization by skin contact.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R39/23/24/25:Toxic: danger of very serious irreversible effects through inhalation, in contact with skin and if swallowed .
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
R11:Highly Flammable.
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R36:Irritating to the eyes.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S13:Keep away from food, drink and animal feeding stuffs .
S24:Avoid contact with skin .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37:Wear suitable protective clothing and gloves .
S16:Keep away from sources of ignition-No smoking .
S7:Keep container tightly closed .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [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 | [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 | [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) |
|
| Company Name: |
Wuhan Topule Gold
|
| Telephone: |
+86-02787215551 19945035818 |
| Website: |
http://www.topule.com/ |
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
|