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Merck
CN

46473

Morantel tartrate hydrate

VETRANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H22N2O6S · xH2O
CAS Number:
26155-31-7
Molecular Weight:
370.42 (anhydrous basis)
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757196
EC Number:
247-481-5
Beilstein/REAXYS Number:
8739506
MDL number:
MFCD01863782

Key Documents

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InChI key

XMDWLUCAURURDF-CIIIEQSVSA-N

InChI

1S/C12H16N2S.C4H6O6.H2O/c1-10-6-9-15-11(10)4-5-12-13-7-3-8-14(12)2;5-1(3(7)8)2(6)4(9)10;/h4-6,9H,3,7-8H2,1-2H3;1-2,5-6H,(H,7,8)(H,9,10);1H2/b5-4+;;/t;1-,2-;/m.1./s1

SMILES string

O.O[C@H]([C@@H](O)C(O)=O)C(O)=O.CN1CCCN=C1\C=C\c2sccc2C

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)

clinical testing

format

neat

Quality Level

200

Related Categories

General description

Chemical structure: tetrahydropyrimidine

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 mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK3796
BCCK0686
BCCG5294
BCCC0974
BCCB8442

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M Várady et al.
Veterinary research communications, 22(5), 299-304 (1998-10-21)
The in vitro activities of thiabendazole, levamisole, pyrantel, morantel and ivermectin against Oesophagostomum spp., the nodular worm of pigs, were determined and compared. The study was carried out using isolates of O. dentatum and O. quadrispinulatum, which had been defined
B Berrag et al.
Journal of helminthology, 72(1), 15-20 (1998-06-26)
A herd of goats naturally infected with lungworm and gastrointestinal nematodes was divided into three groups and treated with either morantel tartrate or fenbendazole at strategic periods, i.e. in June (at pre-mating), in November (at pre-kidding) and in January (at
Beate I Escher et al.
Environmental toxicology and chemistry, 27(4), 909-918 (2008-03-13)
A comparative hazard assessment of the antiparasitics ivermectin, albendazole, and morantel was performed, with a particular focus on bioavailability and uptake into biological membranes. The experimentally determined liposome-water distribution ratio at pH 7 (D(lipw) (pH 7)) of the positively charged
M A Smith et al.
The international journal of biochemistry & cell biology, 31(9), 961-975 (1999-10-26)
(1) The role of fumarate metabolism in the microaerophily of the Campylobacter genus and the effects of therapeutic agents against it were investigated. (2) NMR spectroscopy was employed to determine the properties of Campylobacter fumarase (Fum) and fumarate reductase (Frd).
Seungmae Seo et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 29(27), 8734-8742 (2009-07-10)
We are interested in the positive allosteric modulation of neuronal nicotinic acetylcholine (ACh) receptors and have recently shown that the anthelmintic compound morantel potentiates by enhancing channel gating of the alpha3beta2 subtype. Based on the demonstration that morantel-elicited currents were
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