Skip to Content
Merck
All Photos(1)

Documents

36184

Supelco

Oxamyl

PESTANAL®, analytical standard

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

grade

analytical standard

Quality Level

100

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Signal Word

Danger

Hazard Statements

H300 + H330,H312,H410

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM4176
BCCH2759
BCBZ3973
SZBE083XV
SZB9110XV

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 7

1 of 7

Prosulfocarb PESTANAL®, analytical standard

Supelco

31141

Prosulfocarb

Pirimicarb PESTANAL®, analytical standard

Supelco

45627

Pirimicarb

Flusilazole PESTANAL®, analytical standard

Supelco

45753

Flusilazole

Carbofuran 98%

Sigma-Aldrich

426008

Carbofuran

Novaluron PESTANAL®, analytical standard

Supelco

32419

Novaluron

Metalaxyl PESTANAL®, analytical standard

Supelco

32012

Metalaxyl

Phosmet PESTANAL®, analytical standard

Supelco

36195

Phosmet

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
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
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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service