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45495

Supelco

Fenvalerate

PESTANAL®, analytical standard

Sinonimo/i:

α-Cyano-3-phenoxybenzyl α-(4-chlorophenyl)­iso­valerate

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About This Item

Formula empirica (notazione di Hill):
C25H22ClNO3
Numero CAS:
51630-58-1
Peso molecolare:
419.90
Beilstein:
2025982
Numero CE:
257-326-3
Numero MDL:
MFCD00055324
Codice UNSPSC:
41116107
ID PubChem:
329756787
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(Cl)cc3

InChI

1S/C25H22ClNO3/c1-17(2)24(18-11-13-20(26)14-12-18)25(28)30-23(16-27)19-7-6-10-22(15-19)29-21-8-4-3-5-9-21/h3-15,17,23-24H,1-2H3
NYPJDWWKZLNGGM-UHFFFAOYSA-N

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Applicazioni

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

Azioni biochim/fisiol

Type II pyrethroid. Potent inhibitor of calcineurin (protein phosphatase 2B).

Note legali

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

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Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301,H315,H319,H335,H410

Classi di pericolo

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCD3529
BCCC6546
SZBF174XV
SZBE065XV
SZBC345XV

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Terrence L Adelsbach et al.
Reviews of environmental contamination and toxicology, 176, 137-154 (2002-11-22)
Fenvalerate is listed under Class IV of the U.S. Food and Drug Administration (USFDA) Surveillance Index Classification, indicating a low hazard potential to humans from both exposure and toxicological standpoints; thus, minimal monitoring is required (Reed 1981; Eisler 1992). To
Saskia Knillmann et al.
Ecotoxicology (London, England), 21(7), 1857-1866 (2012-05-11)
Competition is a ubiquitous factor in natural populations and has been reported to alter the ecological impact of xenobiotics. We investigated conditions that mirror the natural variation of environmental factors. For this, different treatments were applied to 96 outdoor pond
Nicole Joußen et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(38), 15206-15211 (2012-09-06)
Worldwide, increasing numbers of insects have evolved resistance to a wide range of pesticides, which hampers their control in the field and, therefore, threatens agriculture. Members of the carboxylesterase and cytochrome P450 monooxygenase superfamilies are prominent candidates to confer metabolic
Chris W Coppin et al.
Insect biochemistry and molecular biology, 42(5), 343-352 (2012-02-04)
Esterases have been implicated in metabolic resistance to synthetic pyrethroids in several insect species but little is yet known of the molecular basis for these effects. In this work modern directed evolution technology was used to test to what extent
Xiaohua Gao et al.
Archives of toxicology, 86(9), 1443-1451 (2012-03-23)
Exposure to fenvalerate was demonstrated to be toxic to the male reproductive system. Our previous data revealed that intracellular calcium plays an important role in regulating the above toxicity, through actions on both T-type calcium channels and endoplasmic reticulum calcium
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