The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
· · COA & SDS available for every product · Same-day shipping on in-stock items Mosapride Citrate - ≥98% , CAS No.112885-42-4
Synonyms
AKOS015895400 | DTXCID5026207 | Mosapride citrate - Adooq Bioscience | (+/-)-4-AMINO-5-CHLORO-2-ETHOXY-N-((4-(P-FLUOROBENZYL)-2-MORPHOLINYL)METHYL)BENZAMIDE CITRATE | MOSAPRIDE CITRATE [WHO-DD] | TAK370 | TAK-370 | Mosapride citrate- Bio-X | TAK-370 citra
Shipped In
Ice chest + Ice pads
🧪
Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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.
Overview A selective SR-4 activator and a SR-3 inhibitor.
Specifications Synonyms
AKOS015895400 | DTXCID5026207 | Mosapride citrate - Adooq Bioscience | (+/-)-4-AMINO-5-CHLORO-2-ETHOXY-N-((4-(P-FLUOROBENZYL)-2-MORPHOLINYL)METHYL)BENZAMIDE CITRATE | MOSAPRIDE CITRATE [WHO-DD] | TAK370 | TAK-370 | Mosapride citrate- Bio-X | TAK-370 citra
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Mosapride citrate is a selective SR-4 agonist and SR-3 antagonist. Increases gastric emptying in rats and stimulates gastric motor activity in conscious dogs.Potent and selective 5-HT 4 agonist. Enhances electrically-evoked ileum contractions (EC 50 = 73
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note
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.
Names and Identifiers Canonical Smiles CCOC1=CC(=C(C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(C=C3)F)Cl)N.C(C(=O)O)C(CC(=O)O)(C(=O)O)O IUPAC Name 4-amino-5-chloro-2-ethoxy-N-[[4-[(4-fluorophenyl)methyl]morpholin-2-yl]methyl]benzamide;2-hydroxypropane-1,2,3-tricarboxylic acid InChIKey HUZTYZBFZKRPFG-UHFFFAOYSA-N INCHI 1S/C21H25ClFN3O3.C6H8O7/c1-2-28-20-10-19(24)18(22)9-17(20)21(27)25-11-16-13-26(7-8-29-16)12-14-3-5-15(23)6-4-14;7-3(8)1-6(13,5(11)12)2-4(9)10/h3-6,9-10,16H,2,7-8,11-13,24H2,1H3,(H,25,27);13H,1-2H2,(H,7,8)(H,9,10)(H,11,12) Isomeric SMILES CCOC1=CC(=C(C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(C=C3)F)Cl)N.C(C(=O)O)C(CC(=O)O)(C(=O)O)O Alternate CAS 112885-42-4 MeSH Entry Terms 4-amino-5-chloro-2-ethoxy-N-((4-(4-fluorobenzyl)-2-morpholinyl)methyl)benzamide;AS 4370;AS-4370;mosapride;mosapride citrate;Mosapride UI05MSP015CT Molecular Weight 614.02 Reaxy-Rn 4288606 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4288606&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 Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Tricarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Tricarboxylic acids and derivatives Alternative Parents Aminophenyl ethers Phenylmethylamines Phenoxy compounds Aniline and substituted anilines Benzylamines Alkyl aryl ethers Aralkylamines Fluorobenzenes Chlorobenzenes Alpha hydroxy acids and derivatives Aryl chlorides Aryl fluorides Morpholines Tertiary alcohols Trialkylamines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Carboximidic acids Carboxylic acids Dialkyl ethers Organic oxides Primary amines Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organofluorides Organochlorides Molecular Framework Not available Substituents Aminophenyl ether - Tricarboxylic acid or derivatives - Phenoxy compound - Phenol ether - Phenylmethylamine - Benzylamine - Aniline or substituted anilines - Alkyl aryl ether - Halobenzene - Fluorobenzene - Aralkylamine - Chlorobenzene - Morpholine - Oxazinane - Alpha-hydroxy acid - Monocyclic benzene moiety - Aryl halide - Benzenoid - Aryl fluoride - Hydroxy acid - Aryl chloride - Tertiary alcohol - Tertiary amine - Tertiary aliphatic amine - Oxacycle - Azacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Organoheterocyclic compound - Dialkyl ether - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organopnictogen compound - Amine - Organic oxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Primary amine - Organooxygen compound - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 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 Soluble in DMSO (100 mM), and ethanol (10 mM). Molecular Weight 614.000 g/mol XLogP3 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 13 Rotatable Bond Count 12 Exact Mass 613.184 Da Monoisotopic Mass 613.184 Da Topological Polar Surface Area 209.000 Ų Heavy Atom Count 42 Formal Charge 0 Complexity 749.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Settings Agree All Decline
Shall we send you a message when we have discounts available?
Remind me later Allow
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
G1924231