532-80-9

Upstream product

• 93818-04-3 5-(4-benzyloxy-phenyl)-3-methyl-oxazolidin-2-one 
• 21213-89-8 1-(4-hydroxy-phenyl)-2-methylamino-ethanone 
• 74-89-5 methylamine 
• 532-80-9 synephrine 

Downstream Products

• 2039-58-9 (+/-)-N,N-Dimethyloctopamine 
• 7339-87-9 4-hydroxyphenylacetaldehyde 
• 101102-83-4 1-(3,5-dibromo-4-hydroxy-phenyl)-2-methylamino-ethanol 
• 614-35-7 (-)-Synephrine 
• 77862-54-5 2,2,3,3,3-Pentafluoro-propionic acid 2-[methyl-(2,2,3,3,3-pentafluoro-propionyl)-amino]-1-[4-(2,2,3,3,3-pentafluoro-propionyloxy)-phenyl]-ethyl ester 
• 128441-37-2 (+)-2-methylamino-1-(4-hydroxyphenyl)ethanol (+)-3-bromocamphor-8-sulphonate 
• 128441-37-2 (-)-2-methylamino-1-(4-hydroxyphenyl)ethanol (-)-3-bromocamphorsulphonate 
• 5985-28-4 (+)p-synephrine hydrochloride 
• 86046-45-9 4-(2-Benzo[1,3]dioxol-5-yl-3-methyl-oxazolidin-5-yl)-phenol 
• 2973-77-5 3,5-dibromo-4-hydroxybenzaldehyde 
• 118-79-6 2,4,6-tribromophenol 
• 292144-13-9 rac-N-(4-chlorobenzyl)-2-(((2-hydroxy-2-(4-hydroxyphenyl)ethyl)(methyl)amino)methyl)-7-methyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamide 
• 86046-48-2 [2-(Benzo[1,3]dioxol-5-yl-methoxy-methoxy)-2-(4-hydroxy-phenyl)-ethyl]-methyl-carbamic acid methyl ester 
• 19588-51-3 N-acetylsynephrine 

Relevant academic research and scientific papers

Direct separation and determination of synephrine enantiomers by high- performance liquid chromatography with electrochemical detection

High-performance liquid chromatography (HPLC) with electrochemical detection using a chiral ligand-exchange column (Sumichiral OA-5000) and a mobile aqueous phase containing 1 mM copper(II) acetate and 20 mM ammonium acetate (pH 6.4) was applied to the di

In-situ and one-step preparation of protein film in capillary column for open tubular capillary electrochromatography enantioseparation

In this work, the phase-transitioned BSA (PTB) film using the mild and fast fabrication process adhered to the capillary inner wall uniformly, and the fabricated PTB film-coated capillary column was applied to realize open tubular capillary electrochromatography (OT-CEC) enantioseparation. The enantioseparation ability of PTB film-coated capillary was evaluated with eight pairs of chiral analytes including drugs and neurotransmitters, all achieving good resolution and symmetrical peak shape. For three consecutive runs, the relative standard deviations (RSD) of migration time for intra-day, inter-day, and column-to-column repeatability were in the range of 0.3%–3.5%, 0.2%–4.9% and 2.1%–7.7%, respectively. Moreover, the PTB film-coated capillary column ran continuously over 300 times with high separation efficiency. Therefore, the coating method based on BSA self-assembly supramolecular film can be extended to the preparation of other proteinaceous capillary columns.

Facile one-pot preparation of chiral monoliths with a well-defined framework based on the thiol-ene click reaction for capillary liquid chromatography

A novel chiral cyclodextrin (CD) monolith was easily prepared via a one-pot process based on the thiol-ene click reaction of allyl-β-CD with pentaerythritol tetra-(3-mercaptopropionate) in a fused-silica capillary. The effects of both the composition of prepolymerization solution and reaction temperature on the morphology, permeability, and selectivity of the β-CD chiral monolith were investigated in detail. The conditions were optimized to fabricate a homogeneous and permeable chiral monolith. In this study, the β-CD monolith was used as the stationary phase of capillary liquid chromatography for the chiral separation of several pharmaceutical enantiomers including flavanone, flurbiprofen, naproxen, synephrine, isoprenaline sulfate, ketoprofen, and atropine sulfate monohydrate. Compared to the previously reported two-step method, this one-pot method for the preparation of a β-CD chiral monolith is simple and time-saving. Moreover, good resolutions were obtained for chiral isomers in a shorter analysis time compared to that reported in the literatures. These results indicate that the thiol-ene click chemistry provides a simple and robust method for the preparation of a chiral β-CD monolith.

Scavenger assisted combinatorial process for preparing libraries of amides, carbamates and sulfonamides

This invention relates to a novel solution phase process for the preparation of amide, carbamate, and sulfonamide combinatorial libraries. These libraries have utility for drug discovery and are used to form wellplate components of novel assay kits.

Chiral separation of drug enantiomers by capillary electrophoresis using succinyl-β-cyclodextrin

A capillary electrophoretic method for the enantiomeric separation of 11 drugs was developed using an uncoated fused-silica capillary and succinyl β-cyclodextrin as a chiral additive. The effect of the pH of the background electrolyte on selectivity and resolution was studied in the range pH 3.3-9.3. Best results were obtained in a neutral medium. Generally, the presence of a hydroxy group at the chiral C-atom of the analyte seems to be essential because similar compounds without a hydroxy group at the chiral centre did not show chiral resolution. In addition to the enantioselective inclusion into the chiral cavity, hydrogen bondings and formation of ion pairs between the negatively charged selector and cationic analytes can be assumed as mechanisms.

Pharmaceutical formula

The present invention concerns a pharmacological vehicle or carrier system, which makes possible administration of the active ingredient with a high absorption thereof in the blood circulation of the patient treated therewith, in particular also in the case of oral administration. The pharmacological vehicle system according to the invention comprises ultrafine particles of a reaction product of a reactive derivative of an at least dibasic inorganic acid or an alkane-carboxylic acid having 2 or 3 carboxyl groups and optionally one or two hydroxy groups, wherein one bond of the dibasic inorganic acid or one carboxy group of the alkane-carboxylic acid is bonded to a pharmacological active ingredient containing a hydroxy group, SH group and/or a primary or secondary amino group having a ractive hydrogen atom on this group, and the other bond is bonded to the free hydroxy group of a glycerolipid having at least one free hydroxy group on the glycerol. The invention further concerns these reaction products and a process for the preparation of ultrafine particles of these reaction products.