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Parbendazole

VETRANAL®, analytical standard

Synonym(s):

Methyl (5-butyl-1H-benzoimidazol-2-yl)carbamate, Methyl 5(6)-butyl-2-benzimidazolecarbamate

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About This Item

Empirical Formula (Hill Notation):
C13H17N3O2
CAS Number:
14255-87-9
Molecular Weight:
247.29
EC Number:
238-133-3
MDL number:
MFCD18910864
UNSPSC Code:
41116107
PubChem Substance ID:
329754214
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

CCCCc1ccc2nc(NC(=O)OC)[nH]c2c1

InChI

1S/C13H17N3O2/c1-3-4-5-9-6-7-10-11(8-9)15-12(14-10)16-13(17)18-2/h6-8H,3-5H2,1-2H3,(H2,14,15,16,17)

InChI key

YRWLZFXJFBZBEY-UHFFFAOYSA-N

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General description

Parbendazole is a carbamate ester-amine. It finds applications in control or treatment of nematode infestations.

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

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

Pictograms

Exclamation markHealth hazard
GHS07,GHS08

Signal Word

Warning

Hazard Statements

H302 - H361fd

Hazard Classifications

Acute Tox. 4 Oral - Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC0411
BCBT1349
SZBF222XV
SZBD267XV
SZBC146XV

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M Korenaga et al.
Experimental parasitology, 55(3), 358-363 (1983-06-01)
Immunogenicity of adult Strongyloides ratti was studied in rats. Immunization of rats by intraduodenal implantation of adult worms could completely inhibit the egg production and hasten the expulsion of challenged worms which were developed from subcutaneously inoculated L3 or were
J C Havercroft et al.
Journal of cell science, 49, 195-204 (1981-06-01)
We have shown that the benzimidazole carbamate, parbendazole, is a potent inhibitor of microtubule assembly in vitro and in vivo. Radiolabelled parbendazole was shown to bind to purified tubulin. Immunofluorescence studies using antitubulin antibody showed that parbendazole effectively depolymerizes cytoplasmic
D R Hennessy et al.
Journal of veterinary pharmacology and therapeutics, 8(3), 270-275 (1985-09-01)
The ability of parbendazole (PBZ) to potentiate co-administered oxfendazole (OFZ) was investigated. Administration of a range (1.35-36.0 mg/kg) of doses of PBZ with 4.53 mg OFZ/kg demonstrated that significant potentiation occurred at 4.5 mg PBZ/kg. At 4.5 mg PBZ/kg, the
R K Sharma et al.
Veterinary parasitology, 24(3-4), 211-220 (1987-05-01)
Adult Ascaridia galli and Heterakis gallinae obtained from the fowl (Gallus gallus) were treated in vitro with 10(-2) to 10(-5) M parbendazole and piperazine adipate for 10-60 min at 38 degrees C. Both the compounds at 10(-2) M caused mortality
E T Lyons et al.
American journal of veterinary research, 41(1), 123-124 (1980-01-01)
Critical tests were conducted in 11 naturally infected horses to evaluate the anthelmintic activity of parbendazole. Single doses at the rates of 30, 20, 10, 5, or 2.5 mg/kg of body weight were administered by stomach tube to 1, 4
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