Pular para o conteúdo
Merck
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Documentos Principais

37895

Supelco

Carbofuran-3-keto

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C12H13NO4
Número CAS:
Peso molecular:
235.24
Beilstein:
1581740
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24
Preço e disponibilidade não estão disponíveis no momento.

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

técnica(s)

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

pf

175-185 °C

adequação

passes test for identity (NMR)

aplicação(ões)

agriculture
environmental

Formato

neat

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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)

chave InChI

WXNZYYXXILQTKX-UHFFFAOYSA-N

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Aplicação

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

Informações legais

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

Pictogramas

Skull and crossbones

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Acute Tox. 3 Oral

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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


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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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