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 Doxylamine Succinate - 10mM in DMSO , Histamine H1 receptor antagonist, CAS No.562-10-7, Histamine H1 receptor antagonist
GRADE & PURITY 10mM in DMSO
Synonyms
Doxylamine succinate|562-10-7|Decapryn|Gittalun|Unisom|Hoggar N|Doxylamine (succinate)|Doxylamine succinate salt|Doxy-sleep-aid|Evigoa D|Decapryn Succinate|Doxylamine hydrogen succinate|Alsadorm|Mereprine|Sedaplus|A-H Injection|Doxylamine succinate (1:1)|
Shipped In
Dry ice packs + Cold packs
🧪
Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 Doxylamine succinate competitively inhibits histamine at H1 receptors with substantial sedative and anticholinergic effects
Specifications Synonyms
Doxylamine succinate | 562-10-7 | Decapryn | Gittalun | Unisom | Hoggar N | Doxylamine (succinate) | Doxylamine succinate salt | Doxy-sleep-aid | Evigoa D | Decapryn Succinate | Doxylamine hydrogen succinate | Alsadorm | Mereprine | Sedaplus | A-H Injection | Doxylamine succinate (1:1) |
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Doxylamine Succinate is an antihistaminic, sedative, and hypnotic. Doxylamine Succinate is also a H1 histamine receptor antagonist.
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Histamine H1 receptor antagonist
Names and Identifiers Canonical Smiles CC(C1=CC=CC=C1)(C2=CC=CC=N2)OCCN(C)C.C(CC(=O)O)C(=O)O IUPAC Name butanedioic acid;N,N-dimethyl-2-(1-phenyl-1-pyridin-2-ylethoxy)ethanamine InChIKey KBAUFVUYFNWQFM-UHFFFAOYSA-N INCHI 1S/C17H22N2O.C4H6O4/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16;5-3(6)1-2-4(7)8/h4-12H,13-14H2,1-3H3;1-2H2,(H,5,6)(H,7,8) Isomeric SMILES CC(C1=CC=CC=C1)(C2=CC=CC=N2)OCCN(C)C.C(CC(=O)O)C(=O)O WGK Germany 2 RTECS US9275000 Molecular Weight 388.46 Reaxy-Rn 3829474 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3829474&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 Benzenoids Class Benzene and substituted derivatives Subclass Benzylethers Intermediate Tree Nodes Not available Direct Parent Benzylethers Alternative Parents Pyridines and derivatives Dicarboxylic acids and derivatives Heteroaromatic compounds Trialkylamines Dialkyl ethers Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Not available Substituents Benzylether - Dicarboxylic acid or derivatives - Pyridine - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Amine - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as benzylethers. These are aromatic ethers with the general formula ROCR' (R = alkyl, aryl; R'=benzene). External Descriptors organic molecular entity 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 Sensitivity Light sensitive Melt Point(°C) 95-98°C Molecular Weight 388.500 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 9 Exact Mass 388.2 Da Monoisotopic Mass 388.2 Da Topological Polar Surface Area 100.000 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 369.000 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.
