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Merck

46473

Supelco

Morantel tartrate hydrate

VETRANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C16H22N2O6S · xH2O
Número de CAS:
Peso molecular:
370.42 (anhydrous basis)
Beilstein/REAXYS Number:
8739506
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

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

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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John Jensen et al.
Environmental toxicology and chemistry, 28(2), 316-323 (2008-09-25)
Soil invertebrates in arable land are potentially exposed to veterinary medicines excreted by husbandry. The toxicity of three widely used pharmaceuticals was therefore investigated with the use of common soil invertebrates exposed in the laboratory in single- or two-species test
M M Martínez-Grueiro
Parasitology research, 88(10), 946-949 (2002-09-05)
Acid phosphatase (AP) activity was detected in 24 h culture media from adult Heligmosomoides polygyrus. Female and male excretion/secretion products showed similar specific activity. For both, the AP had a pH optimum of 4.0 and was inhibited by sodium fluoride
G L Mendz et al.
Archives of biochemistry and biophysics, 321(1), 153-159 (1995-08-01)
The potential of fumarate reductase as a therapeutic target against the human pathogen Helicobacter pylori was investigated by studying the cytotoxicity of morantel, oxantel, and thiabendazole, known to inhibit the enzyme in parasitic worms. Nuclear magnetic resonance spectroscopy was employed
V Raymond et al.
Neuroscience, 101(3), 785-791 (2000-12-13)
Two homomer-forming nicotinic acetylcholine receptor subunits with 47% identity in their amino acid sequences were employed to compare the actions of cholinergic anthelmintics and ivermectin on expressed vertebrate and nematode nicotinic receptors of known molecular composition. Voltage-clamp electrophysiology was used
Christopher T Konek et al.
Journal of the American Chemical Society, 127(45), 15771-15777 (2005-11-10)
It is now known that the untreated discharge of pharmaceuticals into the environment can impact human health and development and lead to increased drug resistance in biota. Here, we present the first direct interface-specific studies that address the mobility of

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