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ABX  advanced biochemical compounds   


Catalogue
Number
Product Order number / Unit

2056 Buprenorphine hydrochloride 2056.0010: 10 mg per vial
Please inquire for customized filling and bulk quantities.

 
Reference standard for 6-O-[11C]-buprenorphine
Controlled substance, license required in most countries.
Molar Mass: 504.10
C29H41NO4 ⋅ HCl
[53152-21-9]
Colourless to off-white crystalline powder packaged in dark glass crimp cap vials.
Purity: > 95 %
Certificates:
CoA; 1H and 13C NMR spectra
Chemical Name:
CA index names: 6,14-Ethenomorphinan-7-methanol, 17-(cyclopropylmethyl)-α-(1,1-dimethylethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α-methyl-, hydrochloride (1:1); 6,14-Ethenomorphinan-7-methanol, 17-(cyclopropylmethyl)-α-(1,1-dimethylethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α-methyl-, hydrochloride, [5α,7α(S)]-; 6,14-Ethenomorphinan-7-methanol, 17-(cyclopropylmethyl)-α-(1,1-dimethylethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α-methyl-, hydrochloride, (αS,5α,7α)-
Synonymes:
Buprederm; Buprenex
Literature:
Luthra S.K. et al. Automated radiosyntheses of [6-O-methyl-11C]-diprenorphine and [6-O-methyl-11C]buprenorphine from 3-O-trityl protected precursors. Appl. Radiat. Isot. 1994, 45, 857-873.
Luthra S.K. et al. Preparation of [11C]buprenorphine - A potential radioligand for the study of the opiate receptor system in vivo. Int. J. Rad. Appl. Instrum. A. 1987, 38, 65-6.
Lever J.R. et al. Facile synthesis of [11C]buprenorphine for positron emission tomographic studies of opioid receptors. J. Rad. Appl. Instrum. A, 1990, 41, 745-52.
Shiue C.Y. et al. A comparison of the brain uptake of N-(cyclopropyl[11C]methyl)norbuprenorphine ([11C]buprenorphine) and N-(cyclopropyl[11C]methyl)nordiprenorphine ([11C]diprenorphine) in baboon using PET. Int. J. Rad. Appl. Instrum. B, 1991, 18, 281-288.
date of product catalogue issue: 10 May 2017

 
 
 

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