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· · COA & SDS available for every product · Same-day shipping on in-stock items Dihydrexidine hydrochloride - ≥98%(HPLC) , CAS No.158704-02-0
Synonyms
( inverted question mark)-trans-10,11-Dihydroxy-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridine hydrochloride | (+/-)-trans-10,11-Dihydroxy-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridinehydrochloride | EU-0100380 | (+/-)-trans-10,11-Dihydroxy-5,6,6a,7,8,12
Storage
Store at 2-8°C,Desiccated
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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 Store at 2-8°C,Desiccated Ships Wet ice 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.
Specifications Synonyms
( inverted question mark)-trans-10, 11-Dihydroxy-5, 6, 6a, 7, 8, 12b-hexahydrobenzo[a]phenanthridine hydrochloride | (+/-)-trans-10, 11-Dihydroxy-5, 6, 6a, 7, 8, 12b-hexahydrobenzo[a]phenanthridinehydrochloride | EU-0100380 | (+/-)-trans-10, 11-Dihydroxy-5, 6, 6a, 7, 8, 12
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
A potent, full efficacy dopamine D1agonist which shows no agonist activity at peripheral D2receptors or adrenoceptors at doses which cause maximal stimulation of D1sites. The compound appears to be fully bioavailable in brain and exhibits profound antipar
Storage
Store at 2-8°C, Desiccated
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1CC2=CC(=C(C=C2C3C1NCC4=CC=CC=C34)O)O.Cl IUPAC Name (6aR,12bS)-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridine-10,11-diol;hydrochloride InChIKey IJYUPBNUPIRQEP-SATBOSKTSA-N INCHI 1S/C17H17NO2.ClH/c19-15-7-10-5-6-14-17(13(10)8-16(15)20)12-4-2-1-3-11(12)9-18-14;/h1-4,7-8,14,17-20H,5-6,9H2;1H/t14-,17-;/m1./s1 Isomeric SMILES C1CC2=CC(=C(C=C2[C@@H]3[C@@H]1NCC4=CC=CC=C34)O)O.Cl Molecular Weight 303.79 Reaxy-Rn 9886887 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9886887&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 Quinolines and derivatives Subclass Benzoquinolines Intermediate Tree Nodes Not available Direct Parent Phenanthridines and derivatives Alternative Parents Tetralins Tetrahydroisoquinolines Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Quaternary ammonium salts Dialkylamines Azacyclic compounds Organooxygen compounds Organic zwitterions Organic chloride salts Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenanthridine - Tetrahydroisoquinoline - Tetralin - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Benzenoid - Quaternary ammonium salt - Secondary aliphatic amine - Azacycle - Organic chloride salt - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Amine - Organic zwitterion - Organic salt - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included. 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 Solvent:water, Max Conc. mg/mL: 3.04, Max Conc. mM: 10; Solvent:DMSO, Max Conc. mg/mL: 15.19, Max Conc. mM: 50 Molecular Weight 303.800 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 0 Exact Mass 303.103 Da Monoisotopic Mass 303.103 Da Topological Polar Surface Area 52.500 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 361.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 Undefined Atom Stereocenter Count 0 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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