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Merck

37895

Supelco

Carbofuran-3-keto

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C12H13NO4
CAS-Nummer:
Molekulargewicht:
235.24
Beilstein:
1581740
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Methode(n)

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

mp (Schmelzpunkt)

175-185 °C

Eignung

passes test for identity (NMR)

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

−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)

InChIKey

WXNZYYXXILQTKX-UHFFFAOYSA-N

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Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

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

Piktogramme

Skull and crossbones

Signalwort

Danger

H-Sätze

P-Sätze

Gefahreneinstufungen

Acute Tox. 3 Oral

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Die Dokumentenbibliothek aufrufen

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%
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
Kwang-Hyeon Liu et al.
Pest management science, 58(1), 57-62 (2002-02-13)
The pharmacokinetics of furathiocarb were studied in vivo in male Sprague-Dawley rats following dermal treatment. HPLC and post-column derivatization were used for the analysis of furathiocarb and its metabolites (carbofuran, 3-hydroxycarbofuran and 3-ketocarbofuran). Carbofuran and 3-hydroxycarbofuran were detected in plasma
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
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

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