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36184

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Oxamyl

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C7H13N3O3S
Numero CAS:
23135-22-0
Peso molecolare:
219.26
Beilstein:
2212753
Numero CE:
245-445-3
Numero MDL:
MFCD00055334
Codice UNSPSC:
41116107
ID PubChem:
329755326
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

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

Impurezze

≤0.5% water (Karl Fischer)

Punto di fusione

95-101 °C

Compatibilità

passes test for identity (NMR)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CNC(=O)O\N=C(/SC)C(=O)N(C)C

InChI

1S/C7H13N3O3S/c1-8-7(12)13-9-5(14-4)6(11)10(2)3/h1-4H3,(H,8,12)/b9-5-
KZAUOCCYDRDERY-UITAMQMPSA-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

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H300 + H330,H312,H410

Classi di pericolo

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 4 Dermal - 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)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCM4176
BCCH2759
BCBZ3973
SZBE083XV
SZB9110XV

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T J Strathmann et al.
Environmental science & technology, 35(12), 2461-2469 (2001-07-04)
The degradation of two oxime carbamate pesticides, oxamyl and methomyl, was investigated in anoxic solutions containing various metal ions and reducing agents. In reagent-free solutions, these carbamates degrade slowly via base-catalyzed elimination. Rates of carbamate degradation are accelerated by Fe(II)
Patrick Chris Wilson et al.
Environmental toxicology and chemistry, 26(2), 201-207 (2007-08-24)
Pesticide export from citrus production areas is a concern in the Indian River Lagoon drainage basin (Florida, USA). These studies evaluated nontarget deposition and losses of the insecticide oxamyl from typical flatwoods citrus production areas in South Florida. Deposition was
V Fayez et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 18(1), 155-159 (1992-01-01)
The effects of single acute oral doses of 1, 2.1, and 3.5 mg/kg oxamyl (a carbamate insecticide) on selected biochemical parameters in male Sprague-Dawley rats were investigated. The animals exhibited significantly decreased weight gain when compared to control animals. The
Rachel K Osborn et al.
Pest management science, 66(3), 253-261 (2009-10-29)
The potential for enhanced degradation of the carbamoyloxime nematicides aldicarb and oxamyl and the organophosphate fosthiazate was investigated in 35 UK agricultural soils. Under laboratory conditions, soil samples received three successive applications of nematicide at 25 day intervals. The second
E Grauer et al.
Toxicology, 242(1-3), 1-6 (2007-10-13)
Severe poisoning by inhibitors of cholinesterase (ChE) enzymes is often associated with prolonged central or peripheral neuronal damage. Oxotremorine is a cholinergic agonist known to induce acute hypothermia. Central and peripheral cholinergic signaling is involved in the induction of hypothermia
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