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69698

Ranitidine N-oxide

analytical standard

Synonym(s):

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

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About This Item

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


grade

analytical standard

Quality Segment

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.[1]

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This Item
PHR1775PHR1773PHR1774
application(s)

forensics and toxicology
pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

grade

analytical standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

assay

≥95.0% (HPLC)

assay

-

assay

-

assay

-

format

neat

format

neat

format

neat

format

neat

impurities

≤10.0% water (calc. from elemental analysis)

impurities

-

impurities

-

impurities

-


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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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)
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



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