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34087

Supelco

Diethofencarb

PESTANAL®, analytical standard

Sinónimos:

Isopropyl N-(3,4-diethoxyphenyl)carbamate

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About This Item

Fórmula empírica (notación de Hill):
C14H21NO4
Número de CAS:
87130-20-9
Peso molecular:
267.32
EC Number:
403-870-3
MDL number:
MFCD00274591
UNSPSC Code:
41116107
PubChem Substance ID:
329754804
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCOc1ccc(NC(=O)OC(C)C)cc1OCC

InChI

1S/C14H21NO4/c1-5-17-12-8-7-11(9-13(12)18-6-2)15-14(16)19-10(3)4/h7-10H,5-6H2,1-4H3,(H,15,16)

InChI key

LNJNFVJKDJYTEU-UHFFFAOYSA-N

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General description

Diethofencarb is a systemic, phenyl-carbamate fungicide, used for the control of gray mold on fruits and vegetables. Its mode of action involves the inhibition of phospholipids and fatty acid biosynthesis in pathogens.

Application

Diethofencarb may be used as an analytical reference standard for the determination of the analyte in peel and pulp of apples using dispersive liquid-liquid microextraction, followed by high-performance liquid chromatography with diode-array detection (HPLC-DAD).
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

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ5843
BCCB4509
BCBW7229
BCBT7292
SZBC146XV

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D W Hollomon et al.
Antimicrobial agents and chemotherapy, 42(9), 2171-2173 (1998-09-16)
Benzimidazoles are important antitubulin agents used in veterinary medicine and plant disease control. Resistance is a practical problem correlated with single amino acid changes in beta-tubulin and is often linked to greater sensitivity to phenylcarbamates. This negative cross-resistance creates opportunities
M Fujimura et al.
Current genetics, 21(4-5), 399-404 (1992-04-01)
Two MBC-resistant mutants of Neurospora crassa, F914 and F939, were sensitive to diethofencarb at a concentration of 0.1 micrograms/ml, while the wild-type strain and other MBC-resistant mutants showed resistance to diethofencarb at a concentration of 100 micrograms/ml. Genetic analysis suggested
K Saito et al.
Xenobiotica; the fate of foreign compounds in biological systems, 21(5), 575-582 (1991-05-01)
1. Age-related changes in metabolism of diethofencarb (DFC) (isopropyl-1,4-diethoxycarbanilate) and hepatic drug-metabolizing enzyme activities were studied in male Sprague-Dawley rats aged 2, 8, 16 and 21 months. 2. Following a single oral dose of 14C-DFC (500 mg/kg), the major route
Rika Kodaka et al.
Journal of agricultural and food chemistry, 51(26), 7730-7737 (2003-12-11)
The unique nitration of the carbamate fungicide diethofencarb (Powmyl, isopropyl 3,4-diethoxycarbanilate) was examined in 14 Japanese soils and three types of clays under the aerobic conditions using the (14)C-labeled compound. Nitration at the 6-position of the 3,4-diethoxyphenyl ring was a
Jing Cheng et al.
International journal of environmental analytical chemistry, 90(11), 845-855 (2010-09-24)
Dispersive liquid-liquid microextraction (DLLME) has been developed for the extraction and preconcentration of diethofencarb (DF) and pyrimethanil (PM) in environmental water. In the method, a suitable mixture of extraction solvent (50 μL carbon tetrachloride) and dispersive solvent (0.75 mL acetonitrile)
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