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Merck
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Key Documents

Otros 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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[Hygienic regulation of the intermediate products of the production of ethsane--cyclohexane hydrochloride and ethylcyclohexylamine hydrochloride in various types of bodies of water].
A K Manenko et al.
Gigiena i sanitariia, (9)(9), 80-81 (1986-09-01)
[Chromatographic analysis of the herbicide cycloate in the soil].
G F Voronova et al.
Gigiena i sanitariia, (8)(8), 46-47 (1989-08-01)
M G Simpson et al.
Neurotoxicology, 26(1), 125-132 (2004-11-06)
The herbicide cycloate (carbamothioic acid, ethyl(cyclohexyl)-S-ethyl ester) given as a single oral dose to rats, caused selective neuronal cell death in two regions in the rat forebrain, the pyramidal neurons of layers II-III throughout the pyriform cortex and in granule
N J Novick et al.
Applied and environmental microbiology, 49(4), 737-743 (1985-04-01)
Low concentrations of propachlor (2-chloro-N-isopropylacetanilide) and alachlor [2-chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide] were not mineralized, cycloate (S-ethyl-N-ethylthiocyclohexanecarbamate) was slowly or not mineralized, and aniline and cyclohexylamine were readily mineralized in sewage and lake water. Propachlor, alachlor, and cycloate were extensively metabolized, but the products
B C Onisko et al.
Biological mass spectrometry, 23(10), 626-636 (1994-10-01)
The metabolism of cycloate, a thiocarbamate herbicide, was investigated in mature radish leaf. Twelve new metabolites were identified by liquid chromatographic/mass spectrometric analysis using fast atom bombardment and packed capillary liquid chromatography columns. Full-scan and tandem mass spectrometric methods were
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