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Merck

36184

Oxamyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C7H13N3O3S
CAS Number:
23135-22-0
Molecular Weight:
219.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755326
EC Number:
245-445-3
Beilstein/REAXYS Number:
2212753
MDL number:
MFCD00055334

Key Documents

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InChI key

KZAUOCCYDRDERY-UITAMQMPSA-N

InChI

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

SMILES string

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

grade

analytical standard

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

Quality Level

100

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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
GHS06,GHS09

signalword

Danger

Hazard Classifications

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

Storage Class

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

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4176
BCCH2759
BCBZ3973

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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
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)
Emmanuel A Tzortzakakis et al.
Pest management science, 59(12), 1311-1320 (2003-12-12)
The root galling index and the densities of eggs in roots and juveniles in soil of the root-knot nematode Meloidogyne javanica (Treub) Chitwood on tomato, and the effect of these on crop yield were assessed in greenhouse experiments applying various
Steven D Linton et al.
Bioorganic & medicinal chemistry letters, 14(10), 2685-2691 (2004-04-28)
Structural modifications were made to a previously described acyl dipeptide caspase inhibitor, leading to the oxamyl dipeptide series. Subsequent SAR studies directed toward the warhead, P2, and P4 regions of this novel peptidomimetic are described herein.
M L Parker et al.
Archives of environmental contamination and toxicology, 39(2), 233-242 (2000-06-28)
The concept of B-esterase buffering against anti-cholinesterase (ChE) insecticide toxicity has been extensively researched in mammalian species. Presumably due to relatively low levels of anti-ChE detoxifying enzyme activity in birds, however, avian species are often more susceptible to the toxic
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