Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

69698

Supelco

Ranitidine N-oxide

analytical standard

Synonym(s):

N-{2-{{{5-[(Dimethyloxidoamino)methyl]-2-furanyl}methyl}thio}ethyl}-N′-methyl-2-nitro-1,1-ethenediamine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C13H22N4O4S
CAS Number:
Molecular Weight:
330.40
Beilstein:
8395193
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤10.0% water (calc. from elemental analysis)

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

CN/C(NCCSCC1=CC=C(CN(C)C)O1)=C\[N+]([O-])=O.O

InChI

1S/C13H22N4O4S/c1-14-13(8-16(18)19)15-6-7-22-10-12-5-4-11(21-12)9-17(2,3)20/h4-5,8,14-15H,6-7,9-10H2,1-3H3/b13-8+

InChI key

DFJVUWAHTQPQCV-MDWZMJQESA-N

General description

Ranitidine N-oxide is a metabolite of the histamine antagonist drug ranitidine, which is prescribed for the treatment of duodenal and gastric ulcers.

Application

Ranitidine N-oxide may be used as an analytical reference standard for the determination of the analyte in biological fluids by high-performance liquid chromatography based technique.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Simple and universal HPLC-UV method to determine cimetidine, ranitidine, famotidine and nizatidine in urine: Application to the analysis of ranitidine and its metabolites in human volunteers
Ashiru, Diane AI , et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 860(2), 235-240 (2007)
M S Lant et al.
Journal of chromatography, 323(1), 143-152 (1985-04-17)
Reversed-phase high-performance liquid chromatography systems for the separation of ranitidine and its metabolites ranitidine-N-oxide, ranitidine-S-oxide, and desmethylranitidine have been developed for use in high-performance liquid chromatography-mass spectrometry. A direct liquid introduction-high-performance liquid chromatography-mass spectrometry system to analyse qualitatively and quantitatively
High-performance liquid chromatographic methods for the determination of ranitidine and its metabolites in biological fluids
Carey PF, et al.
Chromatographia, 19(1), 200-205 (1984)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service