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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)
Ahmed S A Harabawy et al.
Ecotoxicology and environmental safety, 103, 61-67 (2014-01-28)
The present work aimed to evaluate the toxic effects of two sublethal concentrations of carbofuran pesticide (0.16 and 0.49mg/L, for 35 days) on hematological and blood biochemical parameters of catfish, Clarias gariepinus, and to evaluate the genotoxic potential of carbofuran
Jorge Morales et al.
Chemosphere, 89(11), 1267-1271 (2012-06-22)
The influence of humic aggregates in water solution upon the chemical stability of carbofuran (CF) and the carbofuran-derivatives, 3-hydroxy-carbofuran (HCF) and 3-keto-carbofuran (KCF), has been investigated in basic media. An inhibition upon the basic hydrolysis of 3-hydroxy-carbofuran and 3-keto-carbofuran (≈
Ratnesh Kumar Sharma et al.
Disease markers, 32(3), 153-163 (2012-03-02)
Various efforts have been made in past in order to predict the underlying mechanism of pesticide-induced toxicity using in vitro and animal models, however, these predictions may or may not be directly correlated with humans. The present study was designed

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