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Merck

426008

Carbofuran

98%

Sinónimos:

2,3-Dihydro-2,2-dimethyl-7-benzofuranol N-methylcarbamate

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About This Item

Fórmula empírica (notación de Hill):
C12H15NO3
Número CAS:
1563-66-2
Peso molecular:
221.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24866678
EC Number:
216-353-0
Beilstein/REAXYS Number:
1428746
MDL number:
MFCD00041819

Nombre del producto

Carbofuran, 98%

InChI key

DUEPRVBVGDRKAG-UHFFFAOYSA-N

InChI

1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)

SMILES string

CNC(=O)Oc1cccc2CC(C)(C)Oc12

assay

98%

form

crystals

mp

150-153 °C (lit.)

functional group

amine

Quality Level

100

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General description

Carbofuran is an anticholinesterase carbamate, which is commonly used as a pesticide. Its literature data on toxicity have been reviewed. The effect from exposure to carbofuran has been investigated on acetylcholinesterase (AChE) activity in the brain and muscle of common carp (Cyprinus carpio). Degradation studies using ozone, UV radiation and advanced oxidation processes (AOPs) and by photocatalytic degradation have been investigated. Ultra high performance liquid chromatography (UHPLC) method to determine the carbofuran in water samples have been developed with satisfactory results.

wgk

WGK 3

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 1 Oral - Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1

Clase de almacenamiento

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

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
MKCZ5488
MKCX4322
MKCW0953
MKCT1015
MKCQ8959

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Degradation of carbofuran by using ozone, UV radiation and advanced oxidation processes.
Benitez FJ, et al.
Journal of Hazardous Materials, 89(1), 51-65 (2002)
Photocatalytic degradation of carbofuran using semiconductor oxides.
Mahalakshmi M, et al.
Journal of Hazardous Materials, 143(1), 240-245 (2007)
Luís Pedro de Melo Plese et al.
Chemosphere, 60(2), 149-156 (2005-05-26)
The objectives of this work were estimate the reaction rates of hydrolysis of carbosulfan to carbofuran and subsequent degradation of this last compound in irrigated rice fields, and the respective half life, in aquatic environment and soil solution, by mean
Luz E Vera-Avila et al.
Talanta, 88, 553-560 (2012-01-24)
A selective and simple analytical method for the trace level determination of carbofuran in complex environmental and biological samples was developed based on immunoaffinity extraction (IAE) followed by on-line preconcentration and HPLC/UV analysis of the purified extract. The immunosorbent for
Xia Sun et al.
Sensors (Basel, Switzerland), 11(12), 11679-11691 (2012-01-17)
In this paper, an amperometric immunosensor modified with protein A/deposited gold nanocrystals (DpAu) was developed for the ultrasensitive detection of carbofuran residues. First, DpAu were electrodeposited onto the Au electrode surface to absorb protein A (PA) and improve the electrode
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