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Merck

36128

Supelco

Cypermethrin

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C22H19Cl2NO3
Número de CAS:
Peso molecular:
416.30
Beilstein/REAXYS Number:
8444118
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

description

mixture of isomers

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.57

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

SMILES string

CC1(C)C(\C=C(\Cl)Cl)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2

InChI

1S/C22H19Cl2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3

InChI key

KAATUXNTWXVJKI-UHFFFAOYSA-N

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General description

Cypermethrin is a synthetic pyrethroid pesticide, which can find applications in pest control for agriculture in the protection of cotton and vegetable crops. It can also be used in sanitary pest control.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 - STOT SE 3

target_organs

Nervous system, Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificados de análisis (COA)

Lot/Batch Number

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Los clientes también vieron

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1 of 3

Biodegradation of cypermethrin by Micrococcus sp. strain CPN 1
Tallur.NP, et al.
Biodegradation, 19, 77-82 (2008)
Carcinogenic and cocarcinogenic potential of cypermethrin on mouse skin
Shukla Y, et al.
Cancer Letters, 182, 33-41 (2002)
Toxicity of cypermethrin on growth, pigments, and superoxide dismutase of Scenedesmus obliquus
Li X, et al.
Ecotox. Environ. Safety, 60, 188-192 (2005)
George P Lahm et al.
Bioorganic & medicinal chemistry letters, 15(22), 4898-4906 (2005-09-17)
A novel class of anthranilic diamides has been discovered with exceptional insecticidal activity on a range of Lepidoptera. These compounds have been found to exhibit their action by release of intracellular Ca2+ stores mediated by the ryanodine receptor. The discovery
Hassane Adakal et al.
Experimental & applied acarology, 59(4), 483-491 (2012-09-13)
Traditional systems account for 95 % of the livestock produced in Burkina Faso. Tick infestation hampers livestock productivity in this area. However, little information exists on tick-control practices used by livestock farmers. We interviewed 60 stockbreeders working in traditional farming systems

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