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45333

Supelco

Azinphos-methyl

PESTANAL®, analytical standard

Sinonimo/i:

Guthion®, Methyltriazotin

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About This Item

Formula empirica (notazione di Hill):
C10H12N3O3PS2
Numero CAS:
86-50-0
Peso molecolare:
317.32
Beilstein:
280476
Numero CE:
201-676-1
Numero MDL:
MFCD00041814
Codice UNSPSC:
41116107
ID PubChem:
329756655
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

COP(=S)(OC)SCN1N=Nc2ccccc2C1=O

InChI

1S/C10H12N3O3PS2/c1-15-17(18,16-2)19-7-13-10(14)8-5-3-4-6-9(8)11-12-13/h3-6H,7H2,1-2H3
CJJOSEISRRTUQB-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.

Note legali

Guthion is a registered trademark of Makhteshim Chemical Works Ltd.
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

H300 + H330 - H311 - H317 - H410

Classi di pericolo

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 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)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG5166
BCCC6365
BCBV5129
BCBS2969V

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Jianshe Tang et al.
Journal of immunoassay & immunochemistry, 29(4), 356-369 (2008-09-30)
Organophosphorus Pesticides (OPPs) are a group of artificially synthesized substances used in farms to control pests and to enhance agricultural production. Although these compounds show preferential toxicity to insects, they are also toxic to humans and mammals by the same
Silvia Buono et al.
Ecotoxicology (London, England), 21(3), 688-697 (2011-11-22)
The application of many current-use pesticides has increased after the disuse of persistent, bioaccumulative or toxic ones as DDT or chlordane. Many of the used pesticides are considered less dangerous towards the environment for their physico-chemical properties. This study investigated
Luis Claudio Cacciatore et al.
Chemosphere, 88(4), 450-458 (2012-03-23)
In this study, the cholinesterase (ChE) and carboxylesterase (CES) activities present in whole organism homogenates from Planorbarius corneus and their in vitro sensitivity to organophosphorous (OP) pesticides were studied. Firstly, a characterization of ChE and CES activities using different substrates
Jimena Soleño et al.
Pest management science, 68(11), 1451-1457 (2012-06-08)
Resistance to insecticides has been related to application history, genetic factors of the pest and the dynamic within the treated area. The aim of this study was to assess the geographic variation in azinphos-methyl response and the role of esterase
Matthieu Menager et al.
Environmental science & technology, 47(2), 765-772 (2012-12-12)
The photochemical behavior of the pesticide azinphos methyl at the surface of clays (kaolinite, bentonite) and goethite was studied using Suntest setup (λ > 300 nm). The quantum yield on the clays was found to be roughly three times lower
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Protocolli

US EPA Method 8141: GC Analysis of Organophosphorus Pesticides (OP-Pest) on Equity®-5, NPD Detection

analytical standard; Tokuthion, technical grade, pkg of 50 mg; Crotoxyphos; Phorate; Azinphos-ethyl; Diazinon; Azinphos-methyl; Demeton-O; Dimethoate; Chlorpyrifos-methyl

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