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Merck

PHR1089

Supelco

Cimetidine hydrochloride

Pharmaceutical Secondary Standard; Certified Reference Material

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About This Item

Fórmula empírica (notación de Hill):
C10H16N6S · HCl
Número de CAS:
Peso molecular:
288.80
Beilstein/REAXYS Number:
5668216
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

agency

traceable to Ph. Eur. C2175500
traceable to USP 1134073

API family

cimetidine

CofA

current certificate can be downloaded

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

Cl.CN\C(NC#N)=N/CCSCc1nc[nH]c1C

InChI

1S/C10H16N6S.ClH/c1-8-9(16-7-15-8)5-17-4-3-13-10(12-2)14-6-11;/h7H,3-5H2,1-2H3,(H,15,16)(H2,12,13,14);1H

InChI key

QJHCNBWLPSXHBL-UHFFFAOYSA-N

Gene Information

human ... HRH2(3274)

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General description

Cimetidine is a histamine H2-receptor antagonist, widely used to inhibit gastric acid secretion. It finds application in the treatment of gastric and duodenal ulcers.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

Cimetidine may be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical preparations using gas chromatography technique.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAA7168 in the slot below. This is an example certificate only and may not be the lot that you receive.

related product

Referencia del producto
Descripción
Precios

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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GC Determination of famotidine, ranitidine, cimetidine, and metformin in pharmaceutical preparations and serum using methylglyoxal as derivatizing reagent
Majidano AS, et al.
Chromatographia, 75(21-22), 1311-1317 (2012)
M Tolulope Olaleye et al.
Asian Pacific journal of tropical medicine, 6(3), 200-204 (2013-02-05)
To investigate the restorative effect of Pterocarpus erinaceus (P. erinaceus) and homopterocarpin, an isoflavonoid isolated from it, on indomethacin-induced disruption in gastric homeostasis in rats. Adult rats were divided into five groups and fasted for 48 h before treatment. Group
Hiroshi Satoh et al.
The Journal of pharmacology and experimental therapeutics, 344(1), 189-195 (2012-09-26)
Although nonsteroidal anti-inflammatory drugs often cause ulcers in the duodenum in humans, the role of cyclooxygenase (COX) isoforms in the pathogenesis of duodenal ulcers has not been fully elucidated. We examined in cats the 1) ulcerogenic effects of selective COX-1
Renata Longhini et al.
Journal of anatomy, 222(2), 239-247 (2012-12-04)
It has been demonstrated that histamine interferes with the recruitment, formation and activity of osteoclasts via H(1)- and H(2)-receptors. Cimetidine is a H(2)-receptor antagonist used for treatment of gastric ulcers that seems to prevent bone resorption. In this study, a
Christine Brauckmann et al.
Journal of chromatography. A, 1279, 49-57 (2013-01-29)
Cimetidine has been studied as an additive in cancer chemotherapy. It is claimed to reduce the side effects of Cisplatin. This study focuses on possible interactions between Cisplatin and cimetidine on the molecular level. Due to the fact that cimetidine

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