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Merck
CN

34078

Oxyclozanide

VETRANAL®, analytical standard

Synonym(s):

2,3,5-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxybenzamide, 3,3′,5,5′,6-Pentachloro-2′-hydroxysalicylanilide

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About This Item

Empirical Formula (Hill Notation):
C13H6Cl5NO3
CAS Number:
Molecular Weight:
401.46
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
218-904-0
MDL number:
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InChI key

JYWIYHUXVMAGLG-UHFFFAOYSA-N

InChI

1S/C13H6Cl5NO3/c14-4-1-6(16)11(20)8(2-4)19-13(22)9-10(18)5(15)3-7(17)12(9)21/h1-3,20-21H,(H,19,22)

SMILES string

Oc1c(Cl)cc(Cl)cc1NC(=O)c2c(O)c(Cl)cc(Cl)c2Cl

grade

analytical standard

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

Quality Level

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General description

Oxyclozanide is an anthelmintic agent, which can show activity against Fasciola hepatica, a parasitic trematode and hence, can be used in the treatment of liver fluke infections.

Application

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

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Erdal Dinç et al.
Journal of pharmaceutical and biomedical analysis, 28(3-4), 779-788 (2002-05-15)
Four multivariate calibration-prediction techniques, classical least-squares, inverse least-squares, principal component regression and partial least-squares regression were applied to the spectrophotometric multicomponent analysis of a veterinary formulation containing oxfendazole (OXF) and oxyclozanide (OXC) without any separation step. The multivariate calibrations were
B O Fagbemi et al.
Veterinary parasitology, 69(3-4), 231-240 (1997-05-01)
Antigens that were specific to Fasciola gigantica were obtained from the whole worm homogenate of the parasite by immunoaffinity chromatography in cyanogen bromide-activated sepharose 4B columns and used for the production of monoclonal antibodies. The F. gigantica-specific monoclonal antibody was
P F Rolfe et al.
Australian veterinary journal, 64(11), 328-332 (1987-11-01)
Controlled tests were used to assess the efficacy of anthelmintics against immature paramphistomes, predominantly Calicophoron calicophorum, in 127 calves which were exposed to contaminated pasture for 7 weeks, treated and slaughtered. When a combination product of oxyclozanide and levamisole was
S A Spence et al.
Australian veterinary journal, 74(6), 456-459 (1996-12-01)
To determine the effect of treating naturally acquired gastrointestinal nematode and paramphistome infections on milk production in dairy cattle. A field trial. One thousand two hundred and thirty nine dairy cows. Cows were either not treated or treated with 4.5
N A Mohammed-Ali et al.
Journal of veterinary pharmacology and therapeutics, 10(2), 127-133 (1987-06-01)
The pharmacokinetics of oxyclosanide, rafoxanide and closantel were investigated in sheep (n = 5). All three drugs were extensively (greater than 99%) bound to plasma proteins and the plasma concentration/time curve was best described by a tri-exponential equation. Closantel and

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