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Olaquindox

VETRANAL®, analytical standard

Synonyme(s) :

N-(2-Hydroxyethyl)-3-methyl-2-quinoxalinecarboxamide 1,4-dioxide

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About This Item

Formule empirique (notation de Hill):
C12H13N3O4
Numéro CAS:
23696-28-8
Poids moléculaire :
263.25
Numéro CE :
245-832-7
Numéro MDL:
MFCD00210341
Code UNSPSC :
41116107
ID de substance PubChem :
329754726
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

VETRANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

Cc1c(C(=O)NCCO)[n+]([O-])c2ccccc2[n+]1[O-]

InChI

1S/C12H13N3O4/c1-8-11(12(17)13-6-7-16)15(19)10-5-3-2-4-9(10)14(8)18/h2-5,16H,6-7H2,1H3,(H,13,17)

Clé InChI

TURHTASYUMWZCC-UHFFFAOYSA-N

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Description générale

Olaquindox is an antibiotic veterinary drug, used as a growth promoter for pig farming.

Application

Olaquindox may be used as a reference standard in the determination of olaquindox in feed samples using matrix solid-phase dispersion extraction (MSPDE) and hydrophilic interaction ultra-high-pressure liquid chromatography (HILIC-UHPLC) with photodiode array detector.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H334

Classification des risques

Acute Tox. 4 Oral - Resp. Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Équipement de protection individuelle

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

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCH1618
BCBW1743
SZBD099XV
SZBA074XV
SZBA074X

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Xian-Ju Huang et al.
Chemico-biological interactions, 185(3), 227-234 (2010-03-02)
Quinoxaline 1,4-dioxides (QdNOs) derivatives, the potent synthetic antibacterial group used in food-producing animals, are assumed to have pro-oxidant properties. However, how oxidative stress mediated their adrenal toxicity is far from clear. The aim of this study was to assess the
Biodegradability of metronidazole, olaquindox, and tylosin and formation of tylosin degradation products in aerobic soil--manure slurries
Ingerslev F and Halling-Sorensen B
Ecotoxicology and Environmental Safety, 48(3), 311-320 (2001)
Xu Wang et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(5), 1068-1079 (2011-01-27)
To investigate the teratogenic potential and reproductive toxicity of cyadox, a growth promoting agent, Wistar rats (F(0)) were fed with diets containing cyadox (0, 50, 150 and 2500 mg/kg) or olaquindox (150 mg/kg), approximately equivalent to cyadox 5, 15, 250
Tianci Xu et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(7), 2540-2546 (2012-04-25)
The interaction between olaquindox (OLA) and bovine serum albumin (BSA) was investigated using fluorescence, UV-vis absorption and circular dichroism (CD) spectroscopy. The results showed that the fluorescence quenching of BSA by OLA was a static quenching process induced by the
Xu Wang et al.
Regulatory toxicology and pharmacology : RTP, 59(2), 324-333 (2010-12-07)
To investigate the chronic toxicity of cyadox, a growth promoting agent, five groups of Wistar rats (30 rats/group/sex) were fed with the diets containing cyadox (0, 100, 400 and 2000 mg/kg) or olaquindox (400 mg/kg) for 78weeks. There were significant
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