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Documentos

45408

Supelco

Cycloate

PESTANAL®, analytical standard

Sinónimos:

S-Ethyl N-cyclohexyl-N-ethylthiocarbamate

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About This Item

Fórmula empírica (notación de Hill):
C11H21NOS
Número de CAS:
1134-23-2
Peso molecular:
215.36
Beilstein/REAXYS Number:
2937178
EC Number:
214-482-7
MDL number:
MFCD00055341
UNSPSC Code:
41116107
PubChem Substance ID:
329756708
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
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCSC(=O)N(CC)C1CCCCC1

InChI

1S/C11H21NOS/c1-3-12(11(13)14-4-2)10-8-6-5-7-9-10/h10H,3-9H2,1-2H3

InChI key

DFCAFRGABIXSDS-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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

hcodes

H331,H411

Hazard Classifications

Acute Tox. 3 Inhalation - Aquatic Chronic 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ1174
BCBW6197
SZBD120XV
SZB8119XV
SZE8119X

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Berta N Estevinho et al.
Journal of hazardous materials, 338, 85-92 (2017-05-23)
Molinate is a thiocarbamate herbicide used in rice crop protection. As other pesticides, molinate is a recognized environmental pollutant and bio-accumulated by some wildlife forms. Gulosibacter molinativorax ON4
J Czapski et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 18(4-5), 497-503 (1983-08-01)
The influence of cycloate (active component of Ro-Neet 6E) on the biological value and residues in spinach was studied. During the growing season of spinach, cycloate residues decreased rapidly until by harvest time levels 0.0005--0.0008 mg/kg. had been reached. None
T P Suurmeijer et al.
Epilepsia, 42(9), 1160-1168 (2001-10-03)
Part of our research intended to explain "Quality of Life" (QoL) differences between people with epilepsy. To this end, a series of already existing generic and disease-specific health status measures were used. In this study, they were considered as determinants
B Kosinkiewicz et al.
Acta microbiologica Polonica, 33(2), 111-117 (1984-01-01)
The bacteria from Arthrobacter genus isolated from sugar beet rhizosphere were found to produce gallic, protocatechuic, p-hydroxybenzoic, syryngic, vanillic, veratric acids, p-quinone and two unidentified phenolic compounds. The mixture of the bacterial phenolic compounds increased the phytotoxicity of Roneet, inhibiting
Elzbieta G Magnucka et al.
Pest management science, 65(10), 1065-1070 (2009-05-30)
Cycloate inhibits the biosynthesis of very-long-chain fatty acids, the essential constituents of plant waxes and suberin. Fatty acids also serve as precursors of aliphatic carbon chains in resorcinolic lipids, which play a fundamental role in the plant defence system against
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