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Merck

33979

Supelco

Robenidin -hydrochlorid

VETRANAL®, analytical standard

Synonym(e):

1,3-Bis-[(4-chlorbenzyliden)-amino]-guanidin -monohydrochlorid

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About This Item

Empirische Formel (Hill-System):
C15H13Cl2N5 · HCl
CAS-Nummer:
Molekulargewicht:
370.66
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

VETRANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

SMILES String

Cl[H].Clc1ccc(cc1)\C=N\NC(=N)N\N=C\c2ccc(Cl)cc2

InChI

1S/C15H13Cl2N5.ClH/c16-13-5-1-11(2-6-13)9-19-21-15(18)22-20-10-12-3-7-14(17)8-4-12;/h1-10H,(H3,18,21,22);1H/b19-9+,20-10+;

InChIKey

LTWIBTYLSRDGHP-HCURTGQUSA-N

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Allgemeine Beschreibung

Robenidine hydrochloride is a coccidiostat and antibiotic, used in controlling coccidiosis.

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Robenidine hydrochloride has been used as a reference standard in the determination of robenidine hydrochloride in eggs using online solid-phase extraction with liquid chromatography coupled with tandem mass spectrometry (SPE-LC-MS/MS).

Rechtliche Hinweise

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

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Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Binh Nguyen et al.
Biophysical journal, 90(4), 1319-1328 (2005-11-22)
The energetics for binding of a diphenyl diamidine antitrypanosomal agent CGP 40215A to DNA have been studied by spectroscopy, isothermal titration calorimetry, and surface plasmon resonance biosensor methods. Both amidines are positively charged under experimental conditions, but the linking group
J E Peeters et al.
Veterinary parasitology, 29(4), 327-331 (1988-10-01)
Caecal samples were collected from 751 domestic rabbits of various origin and from 1229 diarrhoeic rabbits issued from 61 commercial rabbitries. They were screened for coccidiosis. In 1982, the year of introduction of the anticoccidial robenidine in commercial rabbit feeds
Martin Hansen et al.
Environmental pollution (Barking, Essex : 1987), 157(2), 474-480 (2008-11-04)
The antibacterial potency of eight anticoccidial drugs was tested in a soil bacteria bioassay (pour plate method), EC(50)-values between 2.4 and 19.6 microM were obtained; however, one compound, nicarbazin exhibited an EC(50)-value above the maximum tested concentration (21 microM, 9.1
R Brun et al.
Tropical medicine & international health : TM & IH, 6(5), 362-368 (2001-05-12)
CGP 40 215 is an inhibitor of S-adenosylmethionine decarboxylase, a key enzyme in trypanosomal polyamine biosynthesis. It is highly active against Trypanosoma brucei rhodesiense and T. b. gambiense in vitro and in the corresponding rodent models, and therefore was a
Robin Das Gupta et al.
Antimicrobial agents and chemotherapy, 49(7), 2857-2864 (2005-06-28)
The intraerythrocytic development of Plasmodium falciparum correlates with increasing levels of the polyamines putrescine, spermidine, and spermine in the infected red blood cells; and compartmental analyses revealed that the majority is associated with the parasite. Since depletion of cellular polyamines

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