tabernanthine

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Company Name: BOC Sciences
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Products Intro: Product Name:Tabernanthine
CAS:83-94-3
Purity:97.0% Package:1mg Remarks:BOC Sciences also provides custom synthesis services for Tabernanthine.
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Tabernanthine
CAS:83-94-3
Package:1 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: BioBioPha Co., Ltd.  
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Products Intro: Product Name:Tabernanthine
CAS:83-94-3
Purity:97.0% Package:5mg Remarks:BBP04600
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 021-61312847; 18021002903
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Products Intro: Product Name:tabernanthine
CAS:83-94-3
Purity:HPLC≥97% Package:5mg
Company Name: Chengdu Push Bio-Technology Co., Ltd.  
Tel: 028-85370565-229 18080489829
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Products Intro: Product Name:Tabernanthine
CAS:83-94-3
Purity:95% Package:5mg
tabernanthine Basic information
Product Name:tabernanthine
Synonyms:tabernanthine;13-Methoxyibogamine;Ibogamine, 13-methoxy-
CAS:83-94-3
MF:C20H26N2O
MW:310.43
EINECS:
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Mol File:83-94-3.mol
tabernanthine Structure
tabernanthine Chemical Properties
Melting point 213.5-215°
alpha D20 -40° (acetone)
Boiling point 160 °C
density 1.20±0.1 g/cm3(Predicted)
pka6.04 in 80% methylcellosolve
Safety Information
MSDS Information
tabernanthine Usage And Synthesis
DescriptionAn alkaloid which occurs in Tabernanthe iboga BailI. and also in Stem madenia donnell-smithii R. E. Woodson, this base was first given the formula C21H2SON2, later altered to that given above. The alkaloid forms colourless needles or orthorhombic plates from EtOH and is best purified by sublimation. It has [α]D - 35° and gives an ultraviolet spectrum with absorption maxima at 229, 271 and 299 IIlfJ.. The hydrochloride forms colourless crystals from boiling H20, m.p. 275-7°C; [α]25.5D - 66° (MeOH). This salt is freely soluble in CHCI3, contains one methoxyl group and is unsaturated.
When injected intravenously into dogs, the alkaloid is hypotensive, reduces the reflex hypertension induced by occlusion of the carotids, decreases both the rate and amplitude of respiration and, like Ibogaine (q.v.), increases the hypertension produced by injection of adrenaline. It has also been found to prolong the hypotension which results from the injection of acetylcholine.
ReferencesDelourme-Houde., An .. Pharm. Fr., 4, 30 (1946)
Bartlett, Dickel, Taylor.,J. Amer. Chem. Soc., 80, 126 (1958)
Walls, Collera, Sandoval., Tetrahedron, 2, 173 (1958)
Pharmacology: Delourme-Houde., Ann. Pharm. Fr., 4, 30 (1946)
tabernanthine Preparation Products And Raw materials
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