
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 73851-70-4 |
| Catalog No. | 2A-9092478 |
| Chinese Name | 雷尼替丁-S-氧化物 |
| Synonyms | References |
| Molecular Formula | C13H22N4O4S |
| Molecular Weight | 330.40 |
| Purity | 96.00% |
| Density | 1.265g/cm3 |
| Boiling Point | 527.5ºC at 760 mmHg |
| Storage Condition | Hygroscopic, -20°C Freezer, Under Inert Atmosphere |
| Application | Ranitidine S-oxide is a metabolite of ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2 receptor antagonist with an IC50 of 3.3 μM, which can inhibit gastric secr |
| PubChem ID | 329823605 |
| SMILES | CNC(=C[N+](=O)[O-])NCCS(=O)Cc1ccc(CN(C)C)o1 |
| InChI | InChI=1S/C13H22N4O4S/c1-14-13(9-17(18)19)15-6-7-22(20)10-12-5-4-11(21-12)8-16(2)3/h4-5,9,14-15H,6-8,10H2,1-3H3/b13-9+ |
| InChI Key | SKHXRNHSZTXSLP-UKTHLTGXSA-N |
| Hazard Symbols | transportation |
| Bioactivity | Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion[1][2]. Related Catalog Research Areas >> Metabolic Disease References [1]. Cross DM, et al. Kinetics of ranitidine metabolism in dog and rat isolated hepatocytes. Xenobiotica. 1995 Apr;25(4):367-75. [2]. Leucuta A, et al. A pharmacokinetic interaction study between omeprazole and the H2-receptor antagonist ranitidine. Drug Metabol Drug Interact. 2004;20(4):273-81. Chemical & Physical Properties Density 1.265g/cm3 Boiling Point 527.5ºC at 760 mmHg Molecular Formula C13H22N4O4S Molecular Weight 330.40300 Flash Point 272.8ºC Exact Mass 330.13600 PSA 122.54000 LogP 2.64520 Index of Refraction 1.577 InChIKey SKHXRNHSZTXSLP-UKTHLTGXSA-N SMILES CNC(=C[N+](=O)[O-])NCCS(=O)Cc1ccc(CN(C)C)o1 Storage condition Hygroscopic, -20°C Freezer, Under Inert Atmosphere |
| Use of | Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion[1][2]. Properties Name Ranitidine S-Oxide Synonym More Synonyms Ranitidine S-Oxide Biological Activity Description Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion[1][2]. Related Catalog Research Areas >> Metabolic Disease References [1]. Cross DM, et al. Kinetics of ranitidine metabolism in dog and rat isolated hepatocytes. Xenobiotica. 1995 Apr;25(4):367-75. [2]. Leucuta A, et al. A pharmacokinetic interaction study between omeprazole and the H2-receptor antagonist ranitidine. Drug Metabol Drug Interact. 2004;20(4):273-81. Chemical & Physical Properties Molecular Formula C13H22N4O4S Exact Mass 330.13600 PSA 122.54000 LogP 2.64520 Index of Refraction 1.577 InChIKey SKHXRNHSZTXSLP-UKTHLTGXSA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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