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ADB-Butinaca
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Home RESEARCH CHEMICALS CANNABINOIDS ADB-Butinaca
7-ADD
7-ADD $27.50
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ADB-Butinaca

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Category: CANNABINOIDS
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Description

What is ADB-BUTINACA?

ADB-BUTINACA is potent indole-based cannabinoid and is an agonist of the CB1 and CB2 receptor with EC50 values of 0.52 nM and 0.88 nM respectively. Has been is closely related to MDMB-BUTINACA and results in laboratory tests show many similar reactions. ADB-Butinaca

Showing its potency in tests ADB-BUTINACA in theory will provide results such as, relaxation, mood enhancement, Euphoria and body lightness.

Always store in a cool, dry place for maximum shelf-life. This product is intended for forensic and research applications only. It is therefore NOT intended for human consumption or in-vivo testing of any kind on animals or any living organism.

Kindly let us know so we can ship discretely to your location without it passing through checks . Always reach out through the inquiry form and note that all payments will be process using any acceptable crypto currency but we recommend using bitcoin, ether, bch

ADB-BINACA is a cannabinoid designer drug that has been found as an ingredient in some synthetic cannabis products. It was originally developed by Pfizer as a potential analgesic, and is a potent agonist of the CB1 receptor with a binding affinity (Ki) of 0.33 nM and an EC50 of 14.7 nM.

ADB-BUTINACA

ADB-BUTINACA
ADB-BUTINACA structure.png
Legal status
Legal status
  • CA: Schedule II
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class B
  • US: Schedule I
Identifiers

IUPAC name
CAS Number
  • 2682867-55-4 check
PubChem CID
  • 155907792
ChemSpider
  • 81407832
Chemical and physical data
Formula C18H26N4O2
Molar mass 330.432 g·mol−1
3D model (JSmol)
  • Interactive image

SMILES

InChI

The analogue with a 1-butyl substitution on the indazole ring rather than 1-benzyl has also been sold as a designer drug under the name ADB-BINACA, but is now more commonly referred to as ADB-BUTINACA to avoid confusion with the benzyl compound. It is a similarly potent CB1 agonist, with an EC50 of 6.36 nM

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