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36184

Supelco

Oxamyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C7H13N3O3S
CAS Number:
Molecular Weight:
219.26
Beilstein:
2212753
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

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

impurities

≤0.5% water (Karl Fischer)

mp

95-101 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

SMILES string

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-

InChI key

KZAUOCCYDRDERY-UITAMQMPSA-N

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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

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
Kara C Sorensen et al.
Environmental and molecular mutagenesis, 46(3), 174-181 (2005-05-28)
Pesticides are toxic agents intentionally released into the environment; their use raises public health and environmental concerns. In recent years there has been much attention to the biotic degradation of pesticides. Abiotic mechanisms in the soil can contribute to pesticide

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