Description

Buy 5-MAPB Online

 

5-MAPB or 1-(2-benzofuran-5-yl)-N-methylpropan-2-amine is a brand new chemical from the popular benzofuran family. Chemically speaking, 5-MAPB is the N-Methyl analogue of 5-APB. Other members of the benzofuran family include the very popular 6-APB (Benzo Fury) and 6-APDB. Many researchers will be happy to find 5-MAPB is also a selective 2C seretonin agonist. You can buy 5-MAPB direct from us in the hcl salt form.

Full Chemical Name: 1-(benzofuran-5-yl)-N-methylpropan-2-amine
Systematic IUPAC Name: 1-(benzofuran-5-yl)-N-methylpropan-2-amine
CAS Number:1354631-77-8
ChemSpider Number:32078887
Molecular Formula: C12H15N0
Molecular Mass: 225.714 g/mol

What is 5-MAPB used for?
Due to 5-MAPB being an agonist to the 2C receptor it would be appropriate to begin research by using this 2C receptor infused on a synthetic membrane. As 5-MAPB is so new it would be useful to publish the selectivity it has for this receptor by performing a receptor mapping study using a radio labelled version of 5-MAPB. Further studies could include competitive ligand binding assays with other 2C ligands. 5-MAPB may only be used for in vitro (outside living organism) research unless a specific home office licence is held.

5-MAPB may be used for primary reagent testing, as well as a reference sample for analytical libraries, such as GC/MS, HPLC, NMR and FTIR analysis. Toxicologists and forensic scientists may utilize these chemical analyses.

We have secured a source of 5-MAPB from the only current laboratory to synthesis this exclusive chemical and offer it for sale to a very select few vendors. We have tested the sample batch and are very happy to approve this chemical as pure and ready for immediate research.

We offer recorded delivery as standard to all orders of 5-MAPB. This ensures that all orders are delivered, as a tracking number is issued same day.

All orders of 5-MAPB are strictly not for human consumption and must only be used for legitimate research chemical purposes by customers over the age of 18.

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