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36128

Supelco

Cypermethrin

PESTANAL®, analytical standard

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Empirical Formula (Hill Notation):
C22H19Cl2NO3
CAS Number:
52315-07-8
Molecular Weight:
416.30
Beilstein:
8444118
EC Number:
257-842-9
MDL number:
MFCD00055328
UNSPSC Code:
41116107
PubChem Substance ID:
329755278
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Signal Word

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

WGK

WGK 3

Flash Point(F)

212.0 °F

Flash Point(C)

100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品
危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Toxicity of cypermethrin on growth, pigments, and superoxide dismutase of Scenedesmus obliquus
Li X, et al.
Ecotox. Environ. Safety, 60, 188-192 (2005)
Carcinogenic and cocarcinogenic potential of cypermethrin on mouse skin
Shukla Y, et al.
Cancer Letters, 182, 33-41 (2002)
Biodegradation of cypermethrin by Micrococcus sp. strain CPN 1
Tallur.NP, et al.
Biodegradation, 19, 77-82 (2008)
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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