Rabeprazole sodium - ≥98%(HPLC) , CAS No.117976-90-6

CAS: 117976-90-6 Cat. No.: R138070 Peso molecular: 381.42 Número EC: 629-730-3 PubChem CID: 14720269
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)
Synonyms
Rabeprazole SodiumDR | sodium;2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methylsulfinyl]benzimidazol-1-ide | AS-13338 | FT-0689461 | HMS3373B05 | 3-Ethyl-2-methyl-5-(morpholinomethyl)-6,7-dihydro-1H-indol-4(5H)-one hydrochloride | AKOS015895734 | DTXSI
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25mg
R138070-25mg
3
32,90US$
100mg
R138070-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
94,90US$
250mg
R138070-250mg
1
211,90US$
1g
R138070-1g
2
217,90US$
5g
R138070-5g
2
462,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Rabeprazole SodiumDR | sodium;2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methylsulfinyl]benzimidazol-1-ide | AS-13338 | FT-0689461 | HMS3373B05 | 3-Ethyl-2-methyl-5-(morpholinomethyl)-6, 7-dihydro-1H-indol-4(5H)-one hydrochloride | AKOS015895734 | DTXSI
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Potent and selective irreversible gastric H + /K + ATPase pump inhibitor (IC 50 = 72 nM). Prodrug of sulphenamide. Activates over a greater pH range than omeprazole. Shows antibacterial effects against H. pylori (IC 50 = 290 nM).
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%(HPLC)
Nombres e identificadores
Pubchem Sid504767702
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504767702
Sonrisas canónicasCC1=C(C=CN=C1CS(=O)C2=NC3=CC=CC=C3[N-]2)OCCCOC.[Na+]
IUPAC Namesodium;2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methylsulfinyl]benzimidazol-1-ide
InChIKeyKRCQSTCYZUOBHN-UHFFFAOYSA-N
INCHI1S/C18H20N3O3S.Na/c1-13-16(19-9-8-17(13)24-11-5-10-23-2)12-25(22)18-20-14-6-3-4-7-15(14)21-18;/h3-4,6-9H,5,10-12H2,1-2H3;/q-1;+1
Isómeros SMILES CC1=C(C=CN=C1CS(=O)C2=NC3=CC=CC=C3[N-]2)OCCCOC.[Na+]
WGK Alemania 3
PubChem CID 14720269
Peso molecular 381.42

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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseBenzimidazoles
SubclassSulfinylbenzimidazoles
Intermediate Tree Nodes Not available
Direct ParentSulfinylbenzimidazoles
Alternative Parents Methylpyridines  Alkyl aryl ethers  Benzenoids  Imidazoles  Heteroaromatic compounds  Sulfoxides  Sulfinyl compounds  Dialkyl ethers  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic zwitterions  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Sulfinylbenzimidazole - Alkyl aryl ether - Methylpyridine - Pyridine - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Sulfoxide - Dialkyl ether - Ether - Azacycle - Organic alkali metal salt - Sulfinyl compound - Organic nitrogen compound - Organic zwitterion - Organic salt - Organic sodium salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
DescripciónThis 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 organic sodium salt
Estructura 3D
Modelo de Estructura Química Interactiva





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Homo sapiens (32628 Activities)
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POLI Tchem DNA polymerase iota (116820 Activities)
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ABCC2 Tchem Canalicular multispecific organic anion transporter 1 (1191 Activities)
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KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
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ABCB11 Tchem Bile salt export pump (2311 Activities)
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ABCC3 Tbio Canalicular multispecific organic anion transporter 2 (718 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
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NPC1 Tchem Niemann-Pick C1 protein (18985 Activities)
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GMNN Tbio Geminin (128009 Activities)
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RAB9A Tbio Ras-related protein Rab-9A (22488 Activities)
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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
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ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
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BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
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ABCC4 Tchem Multidrug resistance-associated protein 4 (785 Activities)
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RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
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Objetivos asociados (no humanos)
ampC Beta-lactamase AmpC (62480 Activities)
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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
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Luciferin 4-monooxygenase (66902 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
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SARS-CoV-2 (38078 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot NumberCertificate TypeFechaArticulo
E1905068Certificate of AnalysisJan 18, 2023 R138070
Propiedades químicas y físicas
SolubilidadSolubility in water: Completely soluble; Very soluble in Ethanol,Chloroform; Soluble in Methanol; Insoluble in Ether
SensibilidadHygroscopic,Heat Sensitive
Punto de fusión (°C)150 °C
Peso molecular381.400 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count7
Rotatable Bond Count8
Exact Mass381.112 Da
Monoisotopic Mass381.112 Da
Topological Polar Surface Area81.500 Ų
Heavy Atom Count26
Formal Charge0
Complexity446.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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