oxyacanthine

CAS No.
548-40-3
Chemical Name:
oxyacanthine
Synonyms
vinetine;Oxycanthine;oxyacanthine;6,6',7-Trimethoxy-2,2'-dimethyloxyacanthan-12'-ol;2H-1,24:12,15-Dietheno-6,10-metheno-16H-pyrido[2',3':17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinolin-9-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aR,16aS)-
CBNumber:
CB0902883
Molecular Formula:
C37H40N2O6
Molecular Weight:
608.72
MDL Number:
MOL File:
548-40-3.mol
Last updated:2022-12-21 16:56:50

oxyacanthine Properties

Melting point 216-217°
alpha D20 +131.5° (chloroform)
Boiling point 655.15°C (rough estimate)
Density 1.1648 (rough estimate)
refractive index 1.5300 (estimate)
pka 9.42±0.20(Predicted)
FDA UNII 5BD0KNF4AT

oxyacanthine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation PXT0002048 OXYACANTHINE 95.00% 548-40-3 5MG $503.9 2021-12-16 Buy
Product number Packaging Price Buy
PXT0002048 5MG $503.9 Buy

oxyacanthine Chemical Properties,Uses,Production

Description

This alkaloid was first obtained by Hesse from Berberis vulgaris and is also a minor constituent of other Berberis and Mahonia species. When recrystallized from EtOH it forms clusters of colourless needles, m.p. 208-214°C, the higher melting point given above being obtained in vacuo. It has [α]D + 131.6° (CHC13), a much higher value of + 279° (CHCI3) being given by Gericke and Bruchhausen. The dihydrochloride forms needles, m.p. 270-1°C (vac.); [α] +29 D+ 188.5° (H20) and is only sparingly soluble in dilute HC1; the hydrobromide has m.p. 273-5°C (dec., vac.) and the nitrate forms colourless needles, m.p. 195- 200°C (dec.). The presence of the phenolic hydroxyl group is indicated by the formation of an O-benzoy1 derivative, a potassium salt and the O-methyl ether, giving a hydrochloride, m.p. 261°C. The structure has been deduced from chem_x0002_ical and spectroscopic data. Various colour reactions have been described, e.g. the alkaloid is not coloured by H2S04, gives a yellow colour with HN03 and with molybdic acid in H2S04 produces a violet colour, slowly changing to yellow-green.

Definition

ChEBI: A macrocycle that is oxyacanthan that is substituted by methoxy groups at positions 6, 6', and 7, methyl groups at positions 2 and 2', and a hydroxy group at the 12' position.

oxyacanthine Preparation Products And Raw materials

Raw materials

Preparation Products

oxyacanthine Suppliers

Global( 1)Suppliers
Supplier Tel Email Country ProdList Advantage
Interbioscreen Ltd. -- screen@ibscreen.chg.ru Finland 6178 60
Supplier Advantage
Interbioscreen Ltd. 60
6,6',7-Trimethoxy-2,2'-dimethyloxyacanthan-12'-ol Oxycanthine oxyacanthine vinetine 2H-1,24:12,15-Dietheno-6,10-metheno-16H-pyrido[2',3':17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinolin-9-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aR,16aS)- 548-40-3