- Cyhalothrin
-
-
2026-01-29
- CAS:91465-08-6
- Min. Order:
- Purity: 0.99
- Supply Ability:
- Cyhalothrin
-
- $1.00 / 200KG
-
2026-01-29
- CAS:91465-08-6
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
- λ-Cyhalothrin
-
- $39.00 / 100mg
-
2026-01-19
- CAS:91465-08-6
- Min. Order:
- Purity: 99.94%
- Supply Ability: 10g
|
| Product Name: | λ-Cyhalothrin | | Synonyms: | L-Cyhalothrin,100 μL/mL in MeOH;Cyhalothrin Solution, 100 ng/ in Acetonitrile;3-(2-Chloro-3,3,3-trifluoro-1-propenyl)2,2-dimethyl cyclopropane carboxylic acid, [1alpha (S*),3 alpha(z)-(+)-Cyano(3-phenoxyphenyl)methyl ester;cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethyl cyclopropanecarboxylate;Cyhalon Kung Fu;ICI A0321;OMS 3021;lambda-Cyhalothrin 100mg [91465-08-6] | | CAS: | 91465-08-6 | | MF: | C23H19ClF3NO3 | | MW: | 449.85 | | EINECS: | 415-130-7 | | Product Categories: | INSECTICIDE;AcaricidesPesticides&Metabolites;Alpha sort;C;Agro-Products;Aromatics;CAlphabetic;CO - CZMethod Specific;Insecticides;Oeko-Tex Standard 100;Pesticides;Pesticides&Metabolites;PesticidesPesticides;Pyrethroids | | Mol File: | 91465-08-6.mol |  |
| | λ-Cyhalothrin Chemical Properties |
| Melting point | 49.2°C | | Boiling point | 187-190°C | | density | 1.3225 (estimate) | | storage temp. | Sealed in dry,2-8°C | | solubility | Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly) | | form | Solid | | color | White to off-white | | Merck | 13,2787 | | Stability: | Light Sensitive | | InChI | 1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3/b19-12-/t17-,18+,20-/m0/s1 | | InChIKey | ZXQYGBMAQZUVMI-GCMPRSNUSA-N | | SMILES | CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)c2cccc(Oc3ccccc3)c2 | | LogP | 7.000 | | CAS DataBase Reference | 91465-08-6(CAS DataBase Reference) | | NIST Chemistry Reference | «LAMBDA»-cyhalothrin(91465-08-6) | | EPA Substance Registry System | .lambda.-Cyhalothrin (91465-08-6) |
| Hazard Codes | T+;N,N,T+,Xn | | Risk Statements | 21-25-26-50/53-20/21/22 | | Safety Statements | 1/2-28-36/37/39-38-45-60-61-13 | | RIDADR | UN 2810 6.1/PG 3 | | WGK Germany | 3 | | RTECS | GZ1227780 | | HazardClass | 6.1 | | PackingGroup | III | | Storage Class | 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials | | Hazard Classifications | Acute Tox. 2 Inhalation
Acute Tox. 3 Dermal
Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1 | | Toxicity | LD50 (technical grade) in male, female rats (mg/kg): 79, 56 orally; 632, 696 dermally (Jutsum) |
| Provider | Language |
|
PP321
| English |
| | λ-Cyhalothrin Usage And Synthesis |
| Description | Cyhalothrin is a broad-spectrum pesticide and acaricide that is used to control a wide range of pests in a variety of applications. It belongs to the pyrethroid, a class of synthetic insecticides which has the similar structure and insecticidal activity of the naturally occurring insecticide pyrethrum, derived from the flowers of chrysanthemums. It is commercially used for controlling insects on non-food crops, greenhouses, hospitals, and crops, such as cotton, cereals, hops, ornamentals, potatoes, vegetables, etc. and it targets various kinds of pests, including aphids, Colorado beetles and butterfly larvae. Besides, it is effective to used in public health applications to control insects identified as potential disease vectors, such as cockroaches, mosquitoes, ticks, and flies.
Registered with the EPA in 1988, Cyhalothrin is often preferred as an active ingredient in insecticides because it is proved to be mostly insoluble in water, which is an unlikely water contaminant. It is also nonvolatile, which makes it remain effective for extended periods of time.
| | References | https://en.wikipedia.org/wiki/Cyhalothrin
http://pmep.cce.cornell.edu/profiles/extoxnet/haloxyfop-methylparathion/lambda-cyhalothrin-ext.html
http://www.toxipedia.org/display/toxipedia/Lambda-Cyhalothrin
| | Chemical Properties | olorless to beige powder; or viscous
yellowish-brown liquid. Mild odor. Liquid formulations
containing organic solvents may be flammable. | | Uses | Insecticide; pyrethrin analog | | Uses | Insecticide. | | Definition | ChEBI: (1S)-cis-(alphaR)-cyhalothrin is a cyclopropanecarboxylate ester. | | Agricultural Uses | Insecticide; acaridide: A U.S. EPA restricted Use Pesticide (RUP). Only cyhalothrin is banned for use in EU; not lamda-isomer; CAS 68085-85-8). Used to control a variety of pests in many crops. Also used in structural pest situations.. | | Trade name | CHARGE®; COMMODORE®; DEMAND®; DEMAND CS®; DOUBLE BARREL®; EXCALIBER®; GRENADE®; HALLMARK®; ICON®; IMPASSE®; KARATE®; MATADOR®; NINJA®; PP321®; RATE®; SABER®; SAMURAI®; SCIMITAR®; SENTINEL®; WARRIOR® | | Synthesis | Taking 3-phenoxy-4-fluorobenzaldehyde as raw material, cis-cis-cyfluthrin was prepared by dropwise addition of dichlorochrysanthemoyl chloride (cis-chloroyl chloride), and then the cis-cis-cyfluthrin was prepared by using cyclohexane, n-heptane and isopropanol as solvents, and diisopropylamine-triethylamine and a new type of metal complex ZnCl2-TPP as catalysts, and the reaction of differential isomerization was carried out. Differential isomerization reaction was carried out to obtain the high efficiency cis-cyfluthrin, and the crude product of the high efficiency cis-isomer was filtered after adjusting ph to neutral, and the crude product was recrystallized by methanol and vacuum dried to obtain the high efficiency cis-cyfluthrin vinegar prodrug [2].
| | Potential Exposure | Pyrethroid insecticide and acaridide
used to control a variety of pests in many crops. Also used
in structural pest situations. A United States Environmental
Protection Agency Restricted Use Pesticide (RUP). Only
cyhalothrin is banned for use in EU; not the lamda-isomer
(CAS 68085-85-8). | | Metabolic pathway | The solution and solid-phase photodecomposition of
cyhalothrin involves E/Z and cis/trans isomerization
reactions and frees radical processes leading to
decarboxylation, ester cleavage, proton abstraction,
oxygen scavenging, and reactions with solvent-
generated radicals. The major degradation products
are decarboxylated analogs which are also
isomerized at the cyclopropyl and vinyl groups. In
vitro incubation of 14C-cyhalothrin with honey bee
mid-guts yields the principal metabolite identified as
4-hydroxy-3-phenoxybenzyl alcohol with a small
amount of 3-phenoxybenzoic acid. In vivo metabolism
with honey bees shows the major metabolites 4'-hydroxy-and 2'-hydroxy-3-phenoxybenzyl alcohols
and 4'-hydroxy-3-phenoxybenzoic acid. Prochloraz
delays the metabolism, detoxication, and excretion of
cyhalothrin by inhibition of microsomal oxidation,
effectively enhancing the toxicity to the honey bee. | | Shipping | UN3349 Pyrethroid pesticide, solid
toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous material.
UN3082 Environmentally hazardous substances, liquid,
n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous
material, Technical Name Required.br UN3077 Environmentally hazardous substances, solid,
n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous
material, Technical Name Required. | | Incompatibilities | May react violently with strong oxidi-
zers, bromine, 90% hydrogen peroxide, phosphorus
trichloride, silver powders, or dust. Incompatible with silver
compounds. Mixture with some silver compounds forms
explosive salts of silver oxalate. Hydrolyzed by water | | Waste Disposal | Incineration would be an
effective disposal procedure where permitted. If an efficient
incinerator is not available, the product should be mixed
with large amounts of combustible material and contact
with the smoke should be avoided. In accordance with
40CFR165, follow recommendations for the disposal of
pesticides and pesticide containers. |
| | λ-Cyhalothrin Preparation Products And Raw materials |
|