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32917

Supelco

Prallethrin

PESTANAL®, analytical standard

Sinonimo/i:

(RS)-2-Methyl-4-oxo-3-prop-2-ynylcyclopent-2-enyl (1RS,3RS;1RS,3SR)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate

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About This Item

Formula empirica (notazione di Hill):
C19H24O3
Numero CAS:
23031-36-9
Peso molecolare:
300.39
Numero CE:
245-387-9
Numero MDL:
MFCD03792792
Codice UNSPSC:
41116107
ID PubChem:
329754385
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

Temperatura di conservazione

2-8°C

Stringa SMILE

C\C(C)=C/C1C(C(=O)OC2CC(=O)C(CC#C)=C2C)C1(C)C

InChI

1S/C19H24O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h1,9,14,16-17H,8,10H2,2-6H3
SMKRKQBMYOFFMU-UHFFFAOYSA-N

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Descrizione generale

Prallethrins are classified under the broad category of pyrethroid insecticides that are utilized in agricultural, domestic and industrial applications. They are typically used for protection against mosquitoes, cockroaches as well as other insects.

Applicazioni

Prallethrin may be used as an analytical reference standard for the determination of the analyte in:
  • Sediment samples by dichloromethane (DMC)-based Soxhlet extraction and high-resolution gas chromatography/high-resolution mass spectrometry (HRGC/HRMS).
  • Domestic wastewater samples by ultrasound-assisted dispersive liquid–liquid microextraction (UA-DLLME) combined with capillary GC.

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

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

H302,H331,H410

Classi di pericolo

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

282.2 °F - closed cup

Punto d’infiammabilità (°C)

139 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCJ4484
BCCD7583
BCBZ9640
BCBW3514

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Pyrethroids, pyrethrins, and piperonyl butoxide in sediments by high-resolution gas chromatography/high-resolution mass spectrometry.
Woudneh MB and Oros DR
Journal of Chromatography A, 1135(1), 71-77 (2006)
C H Schaefer et al.
Journal of the American Mosquito Control Association, 6(4), 621-624 (1990-12-11)
Two new pyrethroids, ETOC and lambdacyhalothrin, showed considerable promise against organophosphorus-resistant adults of Culex tarsalis in laboratory tests. In field trials using nonthermal aerosols, applications of both compounds resulted in effective swaths of up to one-half mile. At the highest
Emmanuel M Bhaskar et al.
Journal of medical toxicology : official journal of the American College of Medical Toxicology, 6(1), 27-30 (2010-03-03)
Pyrethroids are common household insecticides. Even though they are less toxic to humans, reports of accidental and suicidal poisoning are not uncommon. Cardiotoxicity due to pyrethroid poisoning is rare. We report a case of cardiac conduction disturbance due to a
T Seki et al.
The Journal of toxicological sciences, 12(4), 397-428 (1987-11-01)
d.d-T80-prallethrin, a pyrethroid insecticide for sanitary use, was administered to Crj : CD (Sprague Dawley) rats at concentrations of 120, 600 or 3,000 ppm in diet for one year to assess the chronic toxicity potential and the reversibility. The summarized
Y Tomigahara et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(9), 839-852 (1994-09-01)
1. Two major metabolites of 14C-labelled (4S,1R)-trans-Etoc[(S)-2-methyl-4-oxo-3-(2-propynyl)cyclopent-2-enyl (1R)-trans-chrysanthemate] were purified using a combination of chromatographic techniques and identified by spectroanalysis (nmr(HMBC) and FAB-, TSP-MS). These were established as new types of S-linked conjugates (sulphonic acid and mercapturic acid types). 2.
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