5720-26-3

Basic information

• Product Name: 5-HYDROXYDOPAMINE HYDROCHLORIDE
• Synonyms: 5-HYDROXYDOPAMINE HYDROCHLORIDE;3,4,5-TRIHYDROXYPHENETHYLAMINE HYDROCHLORIDE;TIMTEC-BB SBB000447;5-(2-aminoethyl)pyrogallol hydrochloride;HydroxydopaminHCl,5-;5-HYDROXYDOPAMINE HYDROCHLORIDE 99%;5-(2-Aminoethyl)-1,2,3-benzenetriol hydrochloride;5-Hydroxydopamine hydrochloride,99%
• CAS NO: 5720-26-3
• Molecular Formula: C₈H₁₁NO₃*ClH
• Molecular Weight: 205.64
• EINECS: 227-223-8
• Mol File: 5720-26-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 218-220 °C(lit.)
• Boiling Point: 414.5 °C at 760 mmHg
• Flash Point: 204.5 °C
• Appearance: off-white to beige to grey-brown powder
• Density: 1.395 g/cm³
• Vapor Pressure: 1.85E-07mmHg at 25°C
• Storage Temp.: −20°C
• CAS DataBase Reference: 5-HYDROXYDOPAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-HYDROXYDOPAMINE HYDROCHLORIDE(5720-26-3)
• EPA Substance Registry System: 5-HYDROXYDOPAMINE HYDROCHLORIDE(5720-26-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 22-26-36
• WGK Germany: 3
• Hazardous Substances Data: 5720-26-3(Hazardous Substances Data)

Usage

Chemical Properties

off-white to beige to grey-brown powder

Uses

5-Hydroxydopamine hydrochloride was used in the preparation of hydrogen peroxide, superoxide radical and hydroxyl radical.

InChI:InChI=1/C8H11NO3/c9-2-1-5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,1-2,9H2/p+1

Upstream product

• 79831-86-0 methyl 3-(benzyloxy)-4,5-dihydroxybenzoate 
• 70424-94-1 methyl 3,4,5-tris(benzyloxy)benzoate 
• 96372-72-4 2-(3,4,5-tris(benzyloxy)phenyl)acetonitrile 
• 79831-88-2 3,4,5-tribenzyloxybenzyl alcohol 
• 96277-83-7 (((5-(chloromethyl)benzene-1,2,3-triyl)tris(oxy))tris(methylene))tribenzene 
• 79831-90-6 2-(3,4,5-trisbenzyloxyphenyl)ethylamine hydrochloride 

Downstream Products

• 1283741-99-0 1-benzyl-1,2,3,4-tetrahydroisoquinoline-6,7,8-triol 

Relevant articles and documents

Biosynthesis. Part 24. Speculative Incorporation Experiments with 1-Benzylisoquinolines and a Logical Approach via C6-C2 and C6-C3 Precursors to the Biosynthesis of Hasubanonine and Protostephanine

Many possible 1-benzyltetrahydroisoquinolines have been examined as possible advanced precursors of the alkaloids hasubanonine (1) and protostephanine (2) in Stephania japonica plants, but none was incorporated significantly.Administration of various precursor molecules having only one aromatic ring, such as tyrosine, has demonstrated that both alkaloids are derived from two different C6-C2 biogenetic units.The subsequent failure of further 1-benzyltetrahydroisoquinolines and bisphenethylamines to be incorporated suggested the intermediacy of either (a) modified 1-benzylisoquinolines or (b) trioxygenated C6-C2 building blocks.Precursors designed to examine the first possibility, such as 1-benzyl-3,4-dihydroisoquinolines or 1-benzyl-1-carboxytetrahydroisoquinolines, were not incorporated into (1) and (2) whereas two 3',4',5'-trioxygenated 2-phenylethylamines were incorporated.These findings allow further delineation of the requirements for later precursors of the alkaloids (1) and (2).