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(Methyl-11C)-L-methionine, also known as Methionine C-11 or UNII-ED857BWP29, is a radiopharmaceutical used in positron emission tomography (PET) imaging. It is synthesized via on-column [11C]methylation using a C18 Sep-Pak Plus as a solid-phase support, achieving high radiochemical yield (78% decay-corrected) and purity (>99%). The method is efficient, automated, and adaptable for other [11C]methylation-based radiopharmaceuticals.

60305-58-0

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60305-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60305-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,0 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60305-58:
(7*6)+(6*0)+(5*3)+(4*0)+(3*5)+(2*5)+(1*8)=90
90 % 10 = 0
So 60305-58-0 is a valid CAS Registry Number.

60305-58-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Methionine-methyl-11C

1.2 Other means of identification

Product number -
Other names UNII-ED857BWP29

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60305-58-0 SDS

60305-58-0Downstream Products

60305-58-0Relevant academic research and scientific papers

Methylation of amide and thiol functions with [11C]methyl triflate, as exemplified by [11C]NMSP, [11C]flumazenil and [11C]methionine

Nagren, Kjell,Halldin, Christer

, p. 831 - 841 (1998)

[11C]Methyl triflate was compared with [11C]methyl iodide as a labelled precursor in the synthesis of PET radioligands through 11C- methylation of amide and thiol functions. [11C]NMSP [11C]flumazenil

Highlighting the versatility of the Tracerlab synthesis modules. Part 2: Fully automated production of [11C]-labeled radiopharmaceuticals using a Tracerlab FXC-Pro

Shao, Xia,Hoareau, Raphael,Runkle, Adam C.,Tluczek, Louis J. M.,Hockley, Brian G.,Henderson, Bradford D.,Scott, Peter J. H.

experimental part, p. 819 - 838 (2012/03/27)

The field of radiochemistry is moving toward exclusive use of automated synthesis modules for production of clinical radiopharmaceutical doses. Such a move not only comes with many advantages but also presents radiochemists with the challenge of re-configuring synthesis modules for production of radiopharmaceuticals that require non-conventional radiochemistry while maintaining full automation. Herein, we continue our series of articles showcasing the versatility of the Tracerlab FX synthesis modules by presenting straightforward, fully automated methods for preparing a range of carbon-11 labeled radiopharmaceuticals using a Tracerlab FXC-Pro. Strategies for production of [11C]acetate, [11C]carfentanil, [ 11C]choline, [11C]3-amino-4-[2-[(di(methyl)amino)methyl] phenyl]sulfanylbenzonitrile ([11C]DASB), (+)-a-[11C] dihydroterabenazine ([11C]DTBZ), [11C]flumazenil ([ 11C]FMZ), meta-hydroxyephedrine ([11C]HED), [ 11C]methionine, [11C]PBR28, [11C]Pittsburgh Compound B ([11C]PiB), 1-[11C]methylpiperidin-4-yl propionate ([11C]PMP), and [11C]raclopride are presented.

High efficiency preparation of L-[S-methyl-11C]methionine by on-column [11C]methylation on C18 Sep-Pak

Pascali, Claudio,Bogni, Anna,Iwata, Ren,Decise, Donatella,Crippa, Flavio,Bombardieri, Emilio

, p. 715 - 724 (2007/10/03)

A novel approach to the synthesis of L-[S-methyl-11C]methionine, (11C]MET) is described which involves a commercial C18 Sep-Pak Plus as a solid-phase support material for the [11C]methylation step. The present method, which uses [11C]CH3I produced by the classical LiAlH4/HI route, supplies [11C]MET ready for injection within 11 min from the end of bombardment (EOB) with a radiochemical yield, decay corrected at EOB, of 78% and a radiochemical purity at the end of synthesis (EOS) higher than 99%. The required setup is extremely simple and easy to automate and can be reset for a further synthesis within few minutes. Moreover, due to its versatility, the method can be utilized for the production of other radiopharmaceuticals requiring a simple [11C]methylation.

Supercritical fluid synthesis and on-line preparative supercritical fluid chromatography of 11C-labelled compounds in supercritical ammonia

Jacobson, Gunilla B.,Markides, Karin E.,Langstroem, Bengt

, p. 418 - 425 (2007/10/03)

An automated supercritical fluid synthesis (SFS) system, designed for reaction and on-line preparative supercritical fluid chromatography (SFC) of 11C-labelled (t1/2 = 20.3 min) compounds in supercritical ammonia, is described. The s

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