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45515

Supelco

Fuberidazole

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C11H8N2O
CAS Number:
3878-19-1
Molecular Weight:
184.19
Beilstein:
153833
EC Number:
223-404-0
MDL number:
MFCD00055496
UNSPSC Code:
41116107
PubChem Substance ID:
329756801
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

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

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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

Signal Word

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 Code

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

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
BCCJ5852
BCBX0840
SZBD178XV
SZB8158XV
SZE8158X

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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
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 Frank et al.
Toxicology letters, 17(3-4), 267-273 (1983-07-01)
The distribution of tritiated 2-(2-furyl)benzimidazole ([3H]FB) in male and pregnant albino mice and male pigmented mice was studied by whole-body autoradiography. The most notable finding was the accumulation of radioactivity in the melanin-containing tissues of the eye, the inner ear
D Picón Zamora et al.
The Analyst, 125(6), 1167-1174 (2000-08-10)
The simultaneous determination of carbendazim, fuberidazole and thiabendazole was accomplished by cross-section (CS) fluorimetry in combination with multivariate calibration algorithms. The total luminescence information of the compounds was used to optimise the linear trajectories of the CS. A comparison between
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