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37895

Supelco

Carbofuran-3-keto

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H13NO4
CAS Number:
16709-30-1
Molecular Weight:
235.24
Beilstein:
1581740
MDL number:
MFCD00155428
UNSPSC Code:
41116107
PubChem Substance ID:
329755711
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

technique(s)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

mp

175-185 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

storage temp.

−20°C

SMILES string

CNC(=O)Oc1cccc2C(=O)C(C)(C)Oc12

InChI

1S/C12H13NO4/c1-12(2)10(14)7-5-4-6-8(9(7)17-12)16-11(15)13-3/h4-6H,1-3H3,(H,13,15)

InChI key

WXNZYYXXILQTKX-UHFFFAOYSA-N

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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.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB1101
BCBR5974V
SZBE097XV
SZBD304XV
SZBA277XV

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Pei Zhou et al.
Science in China. Series C, Life sciences, 48 Suppl 1, 40-47 (2005-08-11)
The DNA damaging effects of the carbamate pesticide carbofuran and its four metabolites (carbofuranphenol, 3-ketocarbofuran, 3-hydrocarbofuran and nitrosocarbofuran) on mice were evaluated by single cell gel electrophoresis (SCGE) assay and micronucleus test. KM mice were exposed to test compounds with
A K Salama
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 33(3), 253-266 (1998-05-30)
Metabolism of carbofuran in pure liquid cultures of A. niger and F. graminearum was investigated. Carbofuran and its metabolites were analyzed by HPLC and TLC. The average recoveries of carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, and 3-ketocarbofuran phenol from fungi media were found
Peter O Otieno et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 45(2), 137-144 (2010-04-15)
This study was undertaken to determine the concentrations of carbofuran residues in water, soil and plant samples from selected sites in the farmlands in Kenya and to demonstrate the impact of Furadan use on the local environment. Soil, water and
M T Ragab et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 18(2), 301-304 (1983-01-01)
Carbofuran was applied over seeded rutabaga cv. York and residues (corrected for recovery) of carbofuran, 3-hydroxy- and 3-ketocarbofuran in the harvested roots averaged 0.15, 0.23 and 0.07 ppm in peel and 0.09, 0.14 and 0.05 ppm in pulp, respectively. Samples
J R Miles et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 16(4), 409-417 (1981-01-01)
In a laboratory study, the persistence of carbofuran and its 3-hydroxy- and 3-keto-metabolites was examined separately over 16 wk in sterile and natural organic (muck) and mineral (loam) soils. Carbofuran was relatively persistent in sterile soils; at 8 wk 77%
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