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· · COA & SDS available for every product · Same-day shipping on in-stock items Midodrine hydrochloride - ≥98% , Adrenergic receptor alpha-1 agonist, CAS No.43218-56-0, Adrenergic receptor alpha-1 agonist
Synonyms
HMS1922O03 | SR-05000001847-3 | (+/-)-2-AMINO-N-(beta-HYDROXY-2,5-DIMETHOXYPHENETHYL)ACETAMIDE MONOHYDROCHLORIDE | 2-Amino-N-(2-(2,5-dimethoxyphenyl)-2-hydroxyethyl)acetamide monohydrochloride | Hipertan | MIDODRINE HYDROCHLORIDE [MI] | ST 1085 HYDROCHLOR
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 Information
Midodrine hydrochloride Midodrine hydrochloride is the hydrochloride salt form of midodrine, an adrenergic alpha-1 agonist used as a vasopressor.
Specifications Synonyms
HMS1922O03 | SR-05000001847-3 | (+/-)-2-AMINO-N-(beta-HYDROXY-2, 5-DIMETHOXYPHENETHYL)ACETAMIDE MONOHYDROCHLORIDE | 2-Amino-N-(2-(2, 5-dimethoxyphenyl)-2-hydroxyethyl)acetamide monohydrochloride | Hipertan | MIDODRINE HYDROCHLORIDE [MI] | ST 1085 HYDROCHLOR
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Midodrine hydrochloride is the hydrochloride salt form of midodrine, an adrenergic alpha-1 agonist used as a vasopressor.
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
Adrenergic receptor alpha-1 agonist
Product Properties ALogP -0.166 hba_count 3 HBD Count 3 Rotatable Bond 6
Names and Identifiers Pubchem Sid 488182460 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182460 Canonical Smiles COC1=CC(=C(C=C1)OC)C(CNC(=O)CN)O.Cl IUPAC Name 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]acetamide;hydrochloride InChIKey MGCQZNBCJBRZDT-UHFFFAOYSA-N INCHI 1S/C12H18N2O4.ClH/c1-17-8-3-4-11(18-2)9(5-8)10(15)7-14-12(16)6-13;/h3-5,10,15H,6-7,13H2,1-2H3,(H,14,16);1H Isomeric SMILES COC1=CC(=C(C=C1)OC)C(CNC(=O)CN)O.Cl Alternate CAS 3092-17-9 Molecular Weight 290.74 Reaxy-Rn 6579688 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6579688&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 Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acid amides Alternative Parents Dimethoxybenzenes Phenoxy compounds Anisoles Alkyl aryl ethers Secondary carboxylic acid amides Secondary alcohols Organopnictogen compounds Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Aromatic alcohols Molecular Framework Aromatic homomonocyclic compounds Substituents Alpha-amino acid amide - P-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Ether - Alcohol - Primary amine - Aromatic alcohol - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Hydrochloride - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. External Descriptors hydrochloride 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 Solubility (25°C) In vitro DMSO: 58 mg/mL (199.49 mM); Sensitivity Moisture sensitive DMSO(mg / mL) Max Solubility 58 DMSO(mM) Max Solubility 199.490954117081 Water(mg / mL) Max Solubility -1 Molecular Weight 290.740 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 6 Exact Mass 290.103 Da Monoisotopic Mass 290.103 Da Topological Polar Surface Area 93.800 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 262.000 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
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