CAS Number91465-08-6
SynonymsLAMOH-CYHALOTHRIN; lambda-Cyhalotrin; LAMBDA CYHALOTHRIN; CYHALOTHRIN LAMBDA; α-cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cyclopropanecarboxylate; λ-Cyhalothrin; Cyhalothrin-Lambda(Cyhalothrin); MFCD02181175; lambda-Cyhalothrin; EINECS 415-130-7; Cyhalothrin
Molecular FormulaC23H19ClF3NO3
Molecular Weight899.700
Purity97%
Density1.33
Boiling Point187-190°C
Melting Point49.2°C
Appearanceliquid
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 91465-08-6 |
| Catalog No. | 2A-9011117 |
| Chinese Name | 三氯氟氰菊酯标准溶液 |
| Synonyms | LAMOH-CYHALOTHRIN; lambda-Cyhalotrin; LAMBDA CYHALOTHRIN; CYHALOTHRIN LAMBDA; α-cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cyclopropanecarboxylate; λ-Cyhalothrin; Cyhalothrin-Lambda(Cyhalothrin); MFCD02181175; lambda-Cyhalothrin; EINECS 415-130-7; Cyhalothrin |
| Molecular Formula | C23H19ClF3NO3 |
| Molecular Weight | 899.700 |
| Purity | 97 |
| Density | 1.33 |
| Boiling Point | 187-190°C |
| Melting Point | 49.2°C |
| Appearance | liquid |
| Storage Condition | 2-8°C |
| Packaging | I; II; III |
| Application | λ-Cyhalothrin is a highly effective, broad-spectrum type II synthetic pyrethroid insecticide containing an α-cyano group. λ-Cyhalothrin is used in a variety of applications to control a variety of ins |
| SMILES | CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1 |
| InChI | 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 |
| InChI Key | ZXQYGBMAQZUVMI-DXCJPMOASA-N |
| Hazard Symbols | 6.1 |
| MSDS | msds/11117_2_91465_08_6.pdf |
| Bioactivity | λ-Cyhalothrin is a high efficiency, broad-spectrum type II synthetic pyrethroid insecticide containing α-cyano group. λ-Cyhalothrin is used to control a wide range of pests in a variety of applications. λ-Cyhalothrin is a neurotoxin that targets sodium channels in the membranes of neurons in the central nervous system[1]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Sodium Channel Research Areas >> Endocrinology Research Areas >> Infection Research Areas >> Neurological Disease In Vitro The mechanism of λ-Cyhalothrin toxicity produces delay in sodium channel inactivation, which leads to persistent depolarization of the nerve membrane. λ-Cyhalothrin produces membrane depolarization, calcium ion infl ux, and neurotransmitter release from rat brain synaptosomes[1]. λ-Cyhalothrin possesses estrogenic properties and has an ability to function as a xenoestrogen promoting human breast carcinoma cell proliferation in vitro[1]. λ-Cyhalothrin has found multiple uses in pest (fleas, cockroaches, flies, and ants) control[1]. λ-Cyhalothrin is highly effective against the malaria transmitting species of Anopheles[1]. In Vivo The effect of λ-Cyhalothrin (i.p.) on memory, movement activity, and co-ordination in mice exposed to bilateral clamping of the carotid arteries (BCCA) is investigated. Neither memory nor movement co-ordination are impaired by BCCA or λ-Cyhalothrin. Exploratory locomotor activity is significantly reduced in the BCCA/LCH group. Spontaneous movement activity is significantly reduced in the BCCA/λ-Cyhalothrin group . Exposure to λ-Cyhalothrin coexisting with BCCA decreases motor activity in the mice in 2 subsequent 30-min[1]. References [1]. Barbara Nieradko-Iwanicka, et al. Effect of Lambda-Cyhalothrin on Memory and Movement in Mice After Transient Incomplete Cerebral Ischemia. Ann Agric Environ Med. 2011;18(1):41-5. Chemical & Physical Properties Density 1.33 Boiling Point 187-190°C Melting Point 49.2°C Molecular Formula C23H19ClF3NO3 Molecular Weight 899.700 Flash Point 255.5ºC Exact Mass 898.201111 PSA 118.64000 LogP 13.08800 Index of Refraction 1.574 InChIKey ZXQYGBMAQZUVMI-DXCJPMOASA-N SMILES CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1 Storage condition 2-8°C |
| Use of | λ-Cyhalothrin is a high efficiency, broad-spectrum type II synthetic pyrethroid insecticide containing α-cyano group. λ-Cyhalothrin is used to control a wide range of pests in a variety of applications. λ-Cyhalothrin is a neurotoxin that targets sodium channels in the membranes of neurons in the central nervous system[1]. Properties Name lambda-cyhalothrin Synonym More Synonyms λ-Cyhalothrin Biological Activity Description λ-Cyhalothrin is a high efficiency, broad-spectrum type II synthetic pyrethroid insecticide containing α-cyano group. λ-Cyhalothrin is used to control a wide range of pests in a variety of applications. λ-Cyhalothrin is a neurotoxin that targets sodium channels in the membranes of neurons in the central nervous system[1]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Sodium Channel Research Areas >> Endocrinology Research Areas >> Infection Research Areas >> Neurological Disease In Vitro The mechanism of λ-Cyhalothrin toxicity produces delay in sodium channel inactivation, which leads to persistent depolarization of the nerve membrane. λ-Cyhalothrin produces membrane depolarization, calcium ion infl ux, and neurotransmitter release from rat brain synaptosomes[1]. λ-Cyhalothrin possesses estrogenic properties and has an ability to function as a xenoestrogen promoting human breast carcinoma cell proliferation in vitro[1]. λ-Cyhalothrin has found multiple uses in pest (fleas, cockroaches, flies, and ants) control[1]. λ-Cyhalothrin is highly effective against the malaria transmitting species of Anopheles[1]. In Vivo The effect of λ-Cyhalothrin (i.p.) on memory, movement activity, and co-ordination in mice exposed to bilateral clamping of the carotid arteries (BCCA) is investigated. Neither memory nor movement co-ordination are impaired by BCCA or λ-Cyhalothrin. Exploratory locomotor activity is significantly reduced in the BCCA/LCH group. Spontaneous movement activity is significantly reduced in the BCCA/λ-Cyhalothrin group . Exposure to λ-Cyhalothrin coexisting with BCCA decreases motor activity in the mice in 2 subsequent 30-min[1]. References [1]. Barbara Nieradko-Iwanicka, et al. Effect of Lambda-Cyhalothrin on Memory and Movement in Mice After Transient Incomplete Cerebral Ischemia. Ann Agric Environ Med. 2011;18(1):41-5. Chemical & Physical Properties Exact Mass 898.201111 PSA 118.64000 LogP 13.08800 Index of Refraction 1.574 InChIKey ZXQYGBMAQZUVMI-DXCJPMOASA-N |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Dangerous Regulations for land transport: 2811 International Dangerous Regulations for sea transport: 2811 International Dangerous Regulations for air transport: 2811 14.2 United Nations shipping name European Land Transport Dangerous Regulations: TOXIC SOLID, ORGANIC, N.O.S. (λ-Cyhalothrin) IMDG Code: TOXIC SOLID, ORGANIC, N.O.S. (λ-Cyhalothrin) International air transport hazard regulations: Toxic solid, organic, n.o.s. (λ-Cyhalothrin) 14.3 Transport hazard categories European Land Transport Danger Regulations: 6.1 International Maritime Transport Danger Regulations: 6.1 International Air Transport Danger Regulations: 6.1 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: Yes International Maritime Transport Dangerous Regulations International Air Transport Dangerous Regulations: No Marine Pollutants (Yes/No): Yes 14.6 Special reminder to users No data available |
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