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Carbofuran

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C12H15NO3
CAS Number:
Molecular Weight:
221.25
Beilstein:
1428746
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

150-153 °C (lit.)

application(s)

agriculture
environmental

format

neat

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)

InChI key

DUEPRVBVGDRKAG-UHFFFAOYSA-N

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General description

Carbofuran belongs to N-methylcarbamate class of chemicals used to control soil-dwelling and foliar-feeding insects on agricultural crops. Carbofuran acts by inhibiting cholinesterase enzyme activity.

Application

Carbofuran may be used as a reference standard for the determination of the analyte:
  • In well water samples by high-performance liquid chromatography employing a variable-wavelength ultraviolet detector set.
  • In fruits and vegetables by monoclonal enzyme immunoassay and high-performance liquid chromatography with fluorescence detection.

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Development of monoclonal antibody-based immunoassays to the N-methylcarbamate pesticide carbofuran.
Abad A, et al.
Journal of Agricultural and Food Chemistry, 47(6), 2475- 2485 (1999)
Determination of carbaryl, carbofuran and methiocarb in cucumbers and strawberries by monoclonal enzyme immunoassays and high-performance liquid chromatography with fluorescence detection: An analytical comparison.
Abad A, et al.
Journal of Chromatography A, 833(1), 3-12 (1999)
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
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
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

Protocols

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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