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46473

Supelco

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)
Beilstein:
8739506
EC Number:
247-481-5
MDL number:
MFCD01863782
UNSPSC Code:
41116107
PubChem Substance ID:
329757196
NACRES:
NA.24

grade

analytical standard

Quality Level

200

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

SMILES string

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

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

InChI key

XMDWLUCAURURDF-CIIIEQSVSA-N

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

Signal Word

Warning

Hazard Statements

H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

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
BCCK3796
BCCK0686
BCCG5294
BCCC0974
BCCB8442

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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).
Diego Rayes et al.
Molecular pharmacology, 71(5), 1407-1415 (2007-02-23)
Nicotinic acetylcholine receptors (nAChRs) are pentameric neurotransmitter-gated ion channels that mediate synaptic transmission throughout the nervous system in vertebrates and invertebrates. Caenorhabditis elegans is a nonmammalian model for the study of the nervous system and a model of parasitic nematodes.
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
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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