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· · COA & SDS available for every product · Same-day shipping on in-stock items Esomeprazole Magnesium - ≥98% , Potassium-transporting ATPase inhibitor, CAS No.161973-10-0, Potassium-transporting ATPase inhibitor
Synonyms
DTXCID501477706 | HMS2878H13 | omeprazole magnesium salt | Omeprazole magnesium [USAN:USP] | Prilosec OTC (TN) | AS-75082 | Esomeprazole(magnesium) | MLS001165732 | Esomeprazole magnesium | OMEPRAZOLE MAGNESIUM [USP-RS] | SW220306-1 | HMS3655A20 | Omepraz
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Esomeprazole Magnesium is a proton pump inhibitor to reduce gastric acid secretion.
Specifications Synonyms
DTXCID501477706 | HMS2878H13 | omeprazole magnesium salt | Omeprazole magnesium [USAN:USP] | Prilosec OTC (TN) | AS-75082 | Esomeprazole(magnesium) | MLS001165732 | Esomeprazole magnesium | OMEPRAZOLE MAGNESIUM [USP-RS] | SW220306-1 | HMS3655A20 | Omepraz
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Esomeprazole magnesium(Nexium) is a proton pump inhibitor which reduces gastric acid secretion through inhibition of H+/K+-ATPase in gastric parietal cells. By inhibiting the functioning of this enzyme, the drug prevents formation of gastric acid.
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Potassium-transporting ATPase inhibitor
Names and Identifiers Pubchem Sid 504757002 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504757002 Canonical Smiles CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[Mg+2] IUPAC Name magnesium;5-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]benzimidazol-1-ide InChIKey KWORUUGOSLYAGD-UHFFFAOYSA-N INCHI 1S/2C17H18N3O3S.Mg/c2*1-10-8-18-15(11(2)16(10)23-4)9-24(21)17-19-13-6-5-12(22-3)7-14(13)20-17;/h2*5-8H,9H2,1-4H3;/q2*-1;+2 Isomeric SMILES CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[Mg+2] Molecular Weight 713.12 Reaxy-Rn 11323158 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11323158&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Benzimidazoles Subclass Sulfinylbenzimidazoles Intermediate Tree Nodes Not available Direct Parent Sulfinylbenzimidazoles Alternative Parents Anisoles Methylpyridines Alkyl aryl ethers Imidazoles Heteroaromatic compounds Sulfoxides Sulfinyl compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Molecular Framework Not available Substituents Sulfinylbenzimidazole - Anisole - Alkyl aryl ether - Methylpyridine - Pyridine - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Sulfoxide - Ether - Azacycle - Sulfinyl compound - Organic nitrogen compound - Organic zwitterion - Organic salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as sulfinylbenzimidazoles. These are polycyclic aromatic compounds containing a sulfinyl group attached at the position 2 of a benzimidazole moiety. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility DMSO 143 mg/mL Water Ethanol 143 mg/mL;Water: <1 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble ) Sensitivity Heat sensitive；Air sensitive；Moisture sensitive x_melt_point_char 172 °C Molecular Weight 713.100 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 14 Rotatable Bond Count 10 Exact Mass 712.199 Da Monoisotopic Mass 712.199 Da Topological Polar Surface Area 163.000 Ų Heavy Atom Count 49 Formal Charge 0 Complexity 453.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 2 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 3
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