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Ranitidine

Ranitidine Structure
CAS No.
66357-35-5
Chemical Name:
Ranitidine
Synonyms
RANITIDINE BASE;Trigger;Ranitidin;RND;U1cex;Zantae;Taural;Zantic;Sampep;Sostril
CBNumber:
CB5480252
Molecular Formula:
C13H22N4O3S
Molecular Weight:
314.4
MOL File:
66357-35-5.mol
Modify Date:
2024/4/26 17:21:34

Ranitidine Properties

Melting point 69-70°C
Boiling point 437.1±45.0 °C(Predicted)
Density 1.184±0.06 g/cm3(Predicted)
storage temp. Desiccate at +4°C
solubility H2O: 1.8 mg/mL
form solid
pka pKa 2.19±0.04 (Uncertain)
color tan
Water Solubility 24.7 mg/mL
Stability Hygroscopic
CAS DataBase Reference 66357-35-5(CAS DataBase Reference)
NIST Chemistry Reference Ranitidine(66357-35-5)
EPA Substance Registry System 1,1-Ethenediamine, N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro- (66357-35-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Safety Statements  22-24/25
WGK Germany  2
RTECS  KM6557000
Toxicity LD50 oral in rat: > 5gm/kg

Ranitidine Chemical Properties,Uses,Production

Description

Ranitidine, a H2-receptor agonist, caused contact dermatitis within the pharmaceutical industry.

Uses

Ranitidine (cas# 66357-35-5) was used as a standard for testing the therapeutic effect of brown propolis extract against aspirin and ethanol- induced gastric ulcers.

Indications

Ranitidine (Zantac) is another H2 receptor antagonist that does not have the same antiandrogen side effects as cimetidine. Note that both cimetidine and ranitidine inhibit the cytochrome P-450 microsomal enzyme system.

General Description

Ranitidine, N-[2-[[[5-(dimethylamino)methyl]-2-furanyl]methyl]thiol] ethyl]-N'-methyl-2-nitro-l,1-ethenediamine (Zantac), is a white solid, which inits hydrochloride salt form is highly soluble in water. It is anaminoalkyl furan derivative with pKa values of 2.7 (sidechain) and 8.2 (dimethylamino). Ranitidine is more potentthan cimetidine, but less potent than famotidine. Likeother H2-antagonists, it does not appear to bind to otherreceptors.
Bioavailability of an oral dose of ranitidine is about 50%and is not significantly affected by the presence of food.Some antacids may reduce ranitidine absorption and shouldnot be taken within 1 hour of administration of this drug. Theplasma half-life of the drug is 2 to 3 hours, and it is excretedalong with its metabolites in the urine. Three metabolites, ranitidineN-oxide, ranitidine S-oxide, and desmethyl ranitidine,have been identified. Ranitidine is only a weak inhibitor ofthe hepatic cytochrome isozymes, and recommended doses ofthe drug do not appear to inhibit the metabolism of otherdrugs. However, there have been isolated reports of drug interactions(warfarin, triazolam) that suggest that ranitidinemay affect the bioavailability of certain drugs by someunidentified mechanism, perhaps by pH-dependent effect onabsorption or a change in volume of distribution.
In addition to being available in various dosage forms asthe hydrochloride salt, ranitidine is also available as a bismuthcitrate salt for use with the macrolide antibiotic clarithromycinin treating patients with an active duodenalulcer associated with H. pylori infection. Eradication of H.pylori reduces the risk of duodenal ulcer recurrence.

Biological Activity

Potent, selective and competitive histamine H 2 receptor antagonist (pA 2 = 6.95-7.2). In vivo, inhibits gastric acid secretion induced by histamine, pentagastrin, bethanecol and food. Also inhibits aspirin-induced gastric lesions.

Contact allergens

Ranitidine, an H2-receptor antagonist, can cause contact dermatitis within the pharmaceutical industry and in health care workers, or may induce systemic drug reactions in patients.

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1,1-Ethenediamine, N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro- 1,1-ethenediamine,n-(2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)eth RANITIDINE TIMTEC-BB SBB006527 N’-Methyl-N-[2-[[[5-(dimethylamino)methyl-2-furanyl]methyl]thio]ethyl]-2-nitro-1-ethenediarnine Sostril Taural Terposen U1cex U1tidine Zantae Zantic RANITIDINE USP Ranitidine (Rantadine) HCl RANITIDINE FORM I RANITIDINE FORM II N'-[2-[[5-(Dimethylaminomethyl)-2-furyl]methylsulfanyl]ethyl]-N-methyl-2-nitro-ethene-1,1-diamine hydrochloride 1,1-ethenediamine,n-(2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethy l)-n’-methyl-2-nitro- n-(2-(((-5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-n’-methyl-2-ni N-[2-[[5-[(Dimethylamino)methyl]furfuryl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine N-[2-[[5-[(Dimethylamino)methyl]furfuryl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethylenediamine tro-1,1-ethenediamine yl)-n-methyl-2-nitro- 1-(Methylamino)-1-[[2-[[5-(dimethylaminomethyl)-2-furyl]methylthio]ethyl]amino]-2-nitroethene N-[1-(Methylamino)-2-nitroethenyl]-2-[5-(dimethylaminomethyl)furan-2-ylmethylthio]ethanamine N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethanediaminehydrochloride Ranitidine hydrochloride COS (E)-N-(2-(((5-((diMethylaMino)Methyl)furan-2-yl)Methyl)thio)ethyl)-N-Methyl-2-nitroethene-1,1-diaMine (E)-N1'-[2-[[5-[(dimethylamino)methyl]-2-furanyl]methylthio]ethyl]-N1-methyl-2-nitroethene-1,1-diamine HSDB 3925 Ranitidine hydrochlo RanitidineQ: What is Ranitidine Q: What is the CAS Number of Ranitidine Q: What is the storage condition of Ranitidine Q: What are the applications of Ranitidine Ranitidine hydrochloride HCL form II USP Ranitidin Trigger RANITIDINE BASE {2-[({5-[(dimethylamino)methyl]furan-2-yl}methyl)sulfanyl]ethyl}[(E)-1-(methylamino)-2-nitroethenyl]amine RANITIDINE HYDROCHLORIDE IH Raticina RND Sampep Ranitidine Reference Standard 66357-35-5 C13H16D6N4O3S C13H22N4O3S Cell Signaling Enzymes Application Index Biochemicals and Reagents BioChemical Substrates Xenobiotics and Drug Metabolism Enzymes, Inhibitors, and Substrates API Active Pharmaceutical Ingredients 66357-35-5