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Merck

31592

Supelco

Amprolium -hydrochlorid

VETRANAL®, analytical standard

Synonym(e):

1-[(4-Amino-2-propyl-5-pyrimidinyl)-methyl]-2-methylpyridiniumchlorid

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About This Item

Lineare Formel:
C14H19N4Cl · HCl
CAS-Nummer:
Molekulargewicht:
315.24
Beilstein:
4118699
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Beschreibung

cationic

Produktlinie

VETRANAL®

Assay

≥98.0% (HPLC)

Haltbarkeit

limited shelf life, expiry date on the label

Mol-Gew.

315.24 g/mol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

clinical testing

Format

neat

SMILES String

[Cl-].Cl[H].CCCc1ncc(C[n+]2ccccc2C)c(N)n1

InChI

1S/C14H19N4.2ClH/c1-3-6-13-16-9-12(14(15)17-13)10-18-8-5-4-7-11(18)2;;/h4-5,7-9H,3,6,10H2,1-2H3,(H2,15,16,17);2*1H/q+1;;/p-1

InChIKey

PJBQYZZKGNOKNJ-UHFFFAOYSA-M

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Anwendung

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

Empfohlene Produkte

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.

Rechtliche Hinweise

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

Piktogramme

Health hazard

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Resp. Sens. 1 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Die Dokumentenbibliothek aufrufen

X Wang et al.
Neuroscience, 144(3), 1045-1056 (2006-12-02)
Thiamine (vitamin B1) deficiency (TD) causes region selective neuronal loss in the brain; it has been used to model neurodegeneration that accompanies mild impairment of oxidative metabolism. The mechanisms for TD-induced neurodegeneration remain incompletely elucidated. Inhibition of protein glycosylation, perturbation
Clara Lemos et al.
European journal of pharmacology, 682(1-3), 37-42 (2012-03-06)
The aim of this study was to characterize the intestinal absorption of thiamine, by investigating the hypothesis of an involvement of Organic Cation Transporter (OCT) family members in this process. [(3)H]-T(+) uptake was found to be: 1) time-dependent, 2) Na(+)-
Studies on the Eimeria of goats at Magadu Dairy Farm SUA, Morogoro, Tanzania.
E N Kimbita et al.
Tropical animal health and production, 41(7), 1263-1265 (2009-02-03)
D Bizon-Zygmańska et al.
Neurochemistry international, 59(2), 208-216 (2011-06-16)
Inhibition of pyruvate (PDHC) and ketoglutarate (KDHC) dehydrogenase complexes induced by thiamine pyrophosphate deficits is known cause of disturbances of cholinergic transmission in the brain, yielding clinical symptoms of cognitive, vegetative and motor deficits. However, particular alterations in distribution of
Mohamed M Ghanem et al.
Preventive veterinary medicine, 84(1-2), 161-170 (2008-02-12)
We compared the therapeutic effect of three anticoccidial drugs (toltrazuril, sulphadimidine and amprolium) in buffalo (Bubalus bubalis) calves experimentally infected with Eimeria bovis (E. bovis) and E. zuernii oocysts (3 x 104oocyst/calf). Buffalo calves (1.5-4 month old, 70-kg body weight)

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