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Merck
CN

N11409

Carbosulfan

analytical standard

Synonym(s):

2,3-Dihydro-2,2-dimethylbenzofuran-7-yl (dibutylaminothio)methylcarbamate

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About This Item

Empirical Formula (Hill Notation):
C20H32N2O3S
CAS Number:
55285-14-8
Molecular Weight:
380.54
UNSPSC Code:
41116107
PubChem Substance ID:
329818501
EC Number:
259-565-9
MDL number:
MFCD00128058

Key Documents

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InChI key

JLQUFIHWVLZVTJ-UHFFFAOYSA-N

InChI

1S/C20H32N2O3S/c1-6-8-13-22(14-9-7-2)26-21(5)19(23)24-17-12-10-11-16-15-20(3,4)25-18(16)17/h10-12H,6-9,13-15H2,1-5H3

SMILES string

CCCCN(CCCC)SN(C)C(=O)Oc1cccc2CC(C)(C)Oc12

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-1063

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

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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.

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup

Regulatory Information

农药列管产品
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N Umetsu et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 15(1), 1-23 (1980-01-01)
The cleavage of the N-S bond in 2,3-dihydro-2,2-dimethyl-7-benzofuranyl (di-n-butylaminosulfenyl) (methyl)carbamate was examined in different buffer solutions (hydrolysis), in buffer solution containing sulfhydryl reagents (thiolysis) and on thin-layer chromatographic plates. In buffer solution and on thin-layer plates, N-S bond cleavage readily
Shuwen Wu et al.
Insect biochemistry and molecular biology, 65, 75-82 (2015-09-13)
Control of Chinese Apolygus lucorum relies heavily on organophosphate insecticides. Here we describe resistance to the organophosphate chlorpyrifos in an A. lucorum strain, BZ-R, which was developed from a field-collected strain (BZ) by selection with chlorpyrifos in the laboratory. BZ-R showed

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