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Merck

426008

Sigma-Aldrich

Carbofuran

98%

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C12H15NO3
CAS-Nummer:
Molekulargewicht:
221.25
Beilstein:
1428746
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

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Qualitätsniveau

Assay

98%

Form

crystals

mp (Schmelzpunkt)

150-153 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

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

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)

InChIKey

DUEPRVBVGDRKAG-UHFFFAOYSA-N

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Allgemeine Beschreibung

Carbofuran is an anticholinesterase carbamate, which is commonly used as a pesticide. Its literature data on toxicity have been reviewed.[1] The effect from exposure to carbofuran has been investigated on acetylcholinesterase (AChE) activity in the brain and muscle of common carp (Cyprinus carpio).[2] Degradation studies using ozone, UV radiation and advanced oxidation processes (AOPs)[3] and by photocatalytic degradation have been investigated.[4] Ultra high performance liquid chromatography (UHPLC) method to determine the carbofuran in water samples have been developed with satisfactory results.[5]

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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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
Li A Lu et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(6), 553-561 (2012-04-13)
Carbofuran, one of the most toxic and biorefractory carbamate compounds, is widely used in insecticides in Taiwan (9-18% of total insecticides production per year). In the present study, a central composite design experiment was used to study the effect of

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