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Parbendazole

VETRANAL®, analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C13H17N3O2
Numéro CAS:
14255-87-9
Poids moléculaire :
247.29
Numéro CE :
238-133-3
Numéro MDL:
MFCD18910864
Code UNSPSC :
41116107
ID de substance PubChem :
329754214
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

VETRANAL®

Durée de conservation

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

Température de stockage

2-8°C

Chaîne SMILES 

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)

Clé InChI

YRWLZFXJFBZBEY-UHFFFAOYSA-N

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Description générale

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.

Informations légales

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

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H361fd

Classification des risques

Acute Tox. 4 Oral - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK8981
BCCC0411
BCBT1349
SZBF222XV
SZBD267XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

D R Hennessy et al.
Journal of veterinary pharmacology and therapeutics, 15(1), 10-18 (1992-03-01)
The effect of intraruminal administration of parbendazole (PBZ) on the flow rate of bile and the pharmacokinetic behaviour of oxfendazole (OFZ) was examined in sheep. PBZ given at 18, 9 and 4.5 mg/kg resulted in a dose-related reduction in bile
E Lacey et al.
Molecular and biochemical parasitology, 19(2), 171-181 (1986-05-01)
The binding of tritiated benzimidazoles (BZs)-albendazole, parbendazole, oxibendazole, mebendazole, oxfendazole and fenbendazole-to crude tubulin extracts from BZ-susceptible and -resistant Haemonchus contortus has been examined. For all BZs, the binding was substantially lower in the resistant isolate. The extent of this
Hiroshi Sato et al.
The Journal of veterinary medical science, 65(4), 453-457 (2003-05-09)
Larva migrans caused by the common raccoon ascarid, Baylisascaris procyonis, is a zoonotic disease of critical importance in North America. Recently we encountered the first proven outbreak of this disease in Japan in domestic rabbits (Oryctolagus cuniculus) in a small
N C Sangster et al.
The Journal of parasitology, 71(5), 645-651 (1985-10-01)
Benzimidazole treatment produced greater effects on microtubule-dependent acetylcholinesterase secretion, the presence of microtubules in intestinal cells, and colchicine binding in susceptible compared with benzimidazole-resistant Trichostrongylus colubriformis. In addition, the binding of benzimidazoles was markedly reduced in preparations from the latter
K E Foster et al.
European journal of biochemistry, 163(3), 449-455 (1987-03-16)
The mutant BEN210 of Physarum polycephalum is highly resistant to a number of benzimidazole carbamate agents, including methylbenzimidazole-2-yl-carbamate and parbendazole. The resistance is conferred by the benD210 mutation in a structural gene for beta-tubulin. This mutant allele encodes a beta-tubulin
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