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Merck

36185

Supelco

Oxycarboxine

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C12H13NO4S
Número de CAS:
Peso molecular:
267.30
Beilstein/REAXYS Number:
1432554
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC1=C(C(=O)Nc2ccccc2)S(=O)(=O)CCO1

InChI

1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

InChI key

AMEKQAFGQBKLKX-UHFFFAOYSA-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.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

>212.0 °F - closed cup

flash_point_c

> 100 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Certificados de análisis (COA)

Lot/Batch Number

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Visite la Librería de documentos

[Methods of identifying and determining plantvax and vitavax in water].
N I Kiseleva
Gigiena i sanitariia, (6)(6), 54-55 (1984-06-01)
R H Balasubramanya et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 15(5), 485-505 (1980-01-01)
Pseudomonas aeruginosa capable of utilizing carboxin and oxycarboxin as sole sources of carbon and nitrogen was isolated from red sandy loam soil perfused with the solutions of these fungicides. The bacterium hydrolyzed oxycarboxin via the intermediate compound 2-(vinylsulphonyl) acetanilide liberating
A C Udeogalanya
Beitrage zur tropischen Landwirtschaft und Veterinarmedizin, 22(1), 91-94 (1984-01-01)
Leaf washing after application of benodanil and oxycarboxin reduced the protectant effect more than the eradicant effect. Oxycarboxin penetrated more rapidly than did benodanil . Residues of benodanil (WP) on the leaf surfaces can be absorbed again later in the

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