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Merck

PS737

Oxamyl

analytical standard

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About This Item

Empirische Formel (Hill-System):
C7H13N3O3S
CAS-Nummer:
Molekulargewicht:
219.26
Beilstein:
2212753
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:

Qualität

analytical standard

Verpackung

ampule of 250 mg

Hersteller/Markenname

Chem Service, Inc. PS-737

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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-

InChIKey

KZAUOCCYDRDERY-UITAMQMPSA-N

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Anwendung

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

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

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)
Connie Hiers et al.
The Journal of the Arkansas Medical Society, 106(7), 134-136 (2009-12-18)
This is a case report and literature review of a 30.8 pound cystosarcoma phyllodes tumor resected in a 54-year-old female. Starting at age 19, the patient had noted a small breast tumor that continued to grow over the years. Pathology
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
Gerardo A Anguiano et al.
Environmental toxicology, 25(4), 327-332 (2009-05-19)
Acetylcholinesterase (AChE) activity has been used to test the exposure of mollusk bivalves to pesticides and other pollutants. The Pacific oyster Crassostrea gigas is a species with a worldwide distribution, and it has a high commercial value. The use of

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