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CN

PS2059

Fuberidazole

analytical standard

Synonym(s):

2-(2-Furanyl)-1H-benzimidazole

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About This Item

Empirical Formula (Hill Notation):
C11H8N2O
CAS Number:
Molecular Weight:
184.19
EC Number:
223-404-0
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
153833
MDL number:
Technical Service
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grade

analytical standard

packaging

ampule of 100 mg

manufacturer/tradename

Chem Service, Inc. PS-2059

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

c1ccc2[nH]c(nc2c1)-c3ccco3

InChI

1S/C11H8N2O/c1-2-5-9-8(4-1)12-11(13-9)10-6-3-7-14-10/h1-7H,(H,12,13)

InChI key

UYJUZNLFJAWNEZ-UHFFFAOYSA-N

Application

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


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wgk

WGK 3

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 Inhalation - Skin Sens. 1 - STOT RE 2

target_organs

Heart

Storage Class

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

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

农药列管产品

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Antonia Moral et al.
Analytica chimica acta, 650(2), 207-213 (2009-09-02)
A supramolecular solvent consisting of vesicles, made up of equimolecular amounts of decanoic acid (DeA) and tetrabutylammonium decanoate (Bu4NDe), dispersed in a continuous aqueous phase, is proposed for the extraction of benzimidazolic fungicides (BFs) from fruits and vegetables. Carbendazim (CB)
A Garrido Frenich et al.
Analytical and bioanalytical chemistry, 375(7), 974-980 (2003-04-23)
The application of the generalised rank annihilation method (GRAM) and the trilinear decomposition (TLD) method to the resolution and quantitation of fluorescence excitation-emission matrices of a ternary mixture of pesticides, carbendazim, fuberidazole, and thiabendazole, with overlapped spectra is described. The
Adrian Frank et al.
Basic & clinical pharmacology & toxicology, 96(4), 325-330 (2005-03-10)
During metabolism of the fungicide 2-(2-furyl)benzimidazole (FB) in mammals, an optically active compound, metabolite A, was isolated. This compound, a principal metabolite in the biological degradation of FB, was isolated from the urine of horse and dog. When studied by