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36184

Supelco

Oxamyl

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C7H13N3O3S
Numéro CAS:
23135-22-0
Poids moléculaire :
219.26
Numéro Beilstein :
2212753
Numéro CE :
245-445-3
Numéro MDL:
MFCD00055334
Code UNSPSC :
41116107
ID de substance PubChem :
329755326
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

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

Impuretés

≤0.5% water (Karl Fischer)

Pf

95-101 °C

Adéquation

passes test for identity (NMR)

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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-

Clé InChI

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.

Informations légales

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

Pictogrammes

Skull and crossbonesEnvironment
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H300 + H330,H312,H410

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCM4176
BCCH2759
BCBZ3973
SZBE083XV
SZB9110XV

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F Lamberti et al.
Mededelingen (Rijksuniversiteit te Gent. Fakulteit van de Landbouwkundige en Toegepaste Biologische Wetenschappen), 67(3), 699-702 (2003-04-17)
Bunches of 25 g of tomato galled roots containing ca. 270 eggs and juveniles/g of Meloidogyne incognita were buried on 29 September 2001 in gauze bags at the depth of 15, 30 and 45 cm in a sandy loam. The
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
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
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
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)
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