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Merck

31469

Supelco

Bensulide

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C14H24NO4PS3
Número de CAS:
Peso molecular:
397.51
Beilstein/REAXYS Number:
2164989
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

Quality Level

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

CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1

InChI

1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3

InChI key

RRNIZKPFKNDSRS-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.

Legal Information

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

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pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Certificados de análisis (COA)

Lot/Batch Number

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George F Antonious
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 45(1), 1-10 (2010-04-15)
Environmentally and economically viable agriculture requires the use of cultivation practices that maximize agrochemical efficacy while minimizing their off-site movement. Bensulide [O, O-diisopropyl S-2-phenylsulfonylaminoethyl phosphorodithioate] is one of the few herbicides from the organophosphate group used for control of weeds
Sheshanka Kesani et al.
Journal of separation science, 41(7), 1663-1673 (2017-12-28)
A niobia-based sol-gel organic-inorganic hybrid sorbent carrying a positively charged C18 ligand (Nb2 O5 -C18 (+ve)) was synthesized to achieve enhanced enrichment capability in capillary microextraction of organophosphorus compounds (which include organophosphorus pesticides and nucleotides) before their online analysis by
T Scott Pinkerton et al.
Methods in molecular biology (Clifton, N.J.), 847, 11-23 (2012-02-22)
Organophosphorus hydrolase (OPH, EC 3.1.8.1) provides a novel function as an alternative genetic marker system for use in many types of plant transformations. OPH is a high-capacity hydrolase with multiple organophosphorus substrates, many of which are neurotoxins and thus used
Yi He et al.
Journal of chromatography. A, 1122(1-2), 7-12 (2006-05-24)
Continuous flow microextraction (CFME) combined with high-performance liquid chromatography-ultraviolet (HPLC-UV) detection has been applied to the analysis of five widely used pesticides, simazine, fensulfothion, etridiazole, mepronil and bensulide, present at trace levels in water samples. CFME employs a single organic
Emily B Lisker et al.
Bulletin of environmental contamination and toxicology, 87(4), 355-360 (2011-06-29)
California's surface water monitoring results from 1991 through 2010 were analyzed to determine whether 12 organophosphorus insecticides and herbicides (i.e., azinphos methyl, bensulide, dimethoate, disulfoton, ethoprop, fenamiphos, methamidophos, methidathion, methyl parathion, naled, phorate, and phosmet) and their degradates have been

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