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Merck

34004

Supelco

Ipronidazole-OH

VETRANAL®, analytical standard

Sinónimos:

2-(1-Methyl-5-nitro-1H-imidazol-2-yl)propan-2-ol, Hydroxy-ipronidazole, IPZOH

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About This Item

Fórmula empírica (notación de Hill):
C7H11N3O3
Número de CAS:
Peso molecular:
185.18
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)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

SMILES string

Cn1c(cnc1C(C)(C)O)[N+]([O-])=O

InChI

1S/C7H11N3O3/c1-7(2,11)6-8-4-5(9(6)3)10(12)13/h4,11H,1-3H3

InChI key

DTHPMNDYKOSVFR-UHFFFAOYSA-N

General description

Ipronidazole-OH is a metabolite of nitroimidazole antibiotics, used in veterinary medicine to combat anaerobic bacterial and parasitic infections.

Application

Ipronidazole-OH may be used as a reference standard in the determination of nitroimidazole drug and its corresponding hydroxy metabolites in aquaculture tissue by ultra-high performance liquid chromatography coupled to tandem mass spectrometry.
Ipronidazole-OH may be used as an analytical reference standard for the determination of the analyte in:
  • Cosmetics using high-performance liquid chromatography coupled to electrospray ionization-tandem mass spectrometry (HPLC-ESI-MS/MS).
  • Aquaculture tissue using ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS).

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

Recommended products

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.

Legal Information

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

Related product

Referencia del producto
Descripción
Precios

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Journal of Chromatography. B, Biomedical Sciences and Applications, 960(6), 105-115 (2014)
Simultaneous determination of 15 nitroimidazoles in cosmetics by HPLC coupled with electrospray ionization-tandem mass spectrometry.
Meng S-X, et al.
Journal of AOAC (Association of Official Analytical Chemists) International, 97(6), 1538-1545 (2014)
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Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(4), 573-581 (2016-11-15)
Nitroimidazoles are not authorised for the treatment of honey bees in the European Union. However, they can be found in honey largely because they are illegally used in apiculture for the treatment of Nosema. The aim of the study was
Chengfei Wang et al.
Food chemistry, 334, 127598-127598 (2020-07-25)
A multi-residue method has been developed for the identification and quantification of 78 compounds from seven different classes of veterinary drugs in eggs. This method was based on dispersive solid phase extraction where mixed-mode cation exchange sorbent was used to
Anton Kaufmann et al.
Journal of the American Society for Mass Spectrometry, 28(12), 2705-2715 (2017-09-14)
Targeted residue screening requires the use of reference substances in order to identify potential residues. This becomes a difficult issue when using multi-residue methods capable of analyzing several hundreds of analytes. Therefore, the capability of in silico fragmentation based on

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