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O5879

Supelco

Ornidazole

analytical standard

Synonym(s):

1-(3-Chloro-2-hydroxypropyl)-2-methyl-5-nitroimidazole

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About This Item

Linear Formula:
C7H10N3O3Cl
CAS Number:
Molecular Weight:
219.63
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

Cc1ncc(n1CC(O)CCl)[N+]([O-])=O

InChI

1S/C7H10ClN3O3/c1-5-9-3-7(11(13)14)10(5)4-6(12)2-8/h3,6,12H,2,4H2,1H3

InChI key

IPWKIXLWTCNBKN-UHFFFAOYSA-N

Application

Ornidazole has been used as a standard in the determination of traces of ornidazole in samples of aquaculture tissue using ultra high performance liquid chromatography coupled with mass spectrometry (UHPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


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Baljit Singh et al.
Colloids and surfaces. B, Biointerfaces, 82(2), 325-332 (2010-10-05)
In view of the antidiarrheal properties of sterculia gum and ornidazole, an attempt has been made to synthesize novel hydrogels by functionalization of sterculia gum with poly(vinylpyrrolidone) (PVP) for release of the model antidiarrheal drug ornidazole. These hydrogels were characterized
Fehmi Tabak et al.
Liver international : official journal of the International Association for the Study of the Liver, 23(5), 351-354 (2004-01-08)
Metronidazole and ornidazole, synthetic nitroimidazole derivatives, are used in the treatment of infections caused by anaerobic bacteria and protozoa. The drugs are well tolerated and serious side effects are very rarely encountered. Hepatotoxicity is a rare side effect and hitherto
Determination of nitroimidazole residues in aquaculture tissue using ultra high performance liquid chromatography coupled to tandem mass spectrometry
Gadaj A, et al.
Journal of Chromatography. B, Biomedical Applications, 960, 105-115 (2014)
Jie Zhao et al.
Journal of hazardous materials, 229-230, 151-158 (2012-06-22)
Nanoparticle of Bi(5)Nb(3)O(15) doped with Y(3+) was prepared for the first time by the sol-gel method combined with impregnation. The degradation of Ornidazole reacting with Y(3+)-Bi(5)Nb(3)O(15) was investigated to explore the feasibility of using Y(3+)-Bi(5)Nb(3)O(15) to treat antibiotics in wastewater.
Subhash S Vaghani et al.
Carbohydrate research, 347(1), 76-82 (2011-11-22)
In the present study, carboxymethyl chitosan was prepared from chitosan, crosslinked with glutaraldehyde and evaluated in vitro as a potential carrier for colon targeted drug delivery of ornidazole. Ornidazole was incorporated at the time of crosslinking of carboxymethyl chitosan. The

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