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    AB-CHMINACA

    $250.00$1,200.00

    Buy AB-CHMINACA UK, Europe in our Globalhomemed.com online shop with fast worldwide delivery! The best AB-CHMINACA for sale you will find here!

    AB-CHMINACA

    Product Description
    AB-CHMINACA for sale
    AB-FUBINACA is an indazole-based synthetic cannabinoid (CB) with 10-fold higher affinity relating to the main CB1 receptor (Ki = 0.9 nM) in contrast to JWH 018 .

    AB-FUBINACA was initially synthesized by Pfizer, Inc. as an effective powerful CB1 receptor modulator for possible therapeutic usage, however not too long ago had been discovered together with AB-PINACA in prohibited herbal products.

    AB-CHMINACA is structurally relevant to AB-FUBINACA which includes a cyclohexyl group replaced for the 4-fluorophenyl group. The physical and toxicological attributes associated with the substance haven’t been identified. The product was created for research and forensic purposes.

    This fine research chemical in our laboratory. We can ensure you that when you order from us you will get a high purity research chemical for your research purspose.

    This research chemical is not intended for human consumption. This cannabinoid ship direct from our lab to any country in the world.

    Dosage
    Presumes no tolerance

    Threshold < 1 mg Light 1 – 2 mg

    Common 1 – 3 mg

    Strong 4 – 5 mg

    Heavy > 5 mg

    Duration
    Total 1 – 2 hours
    Onset 0 – 20 minutes
    Peak 30 – 60 minutes
    Offset 10 – 20 minutes
    Afterglow 15 – 30 minutes

     

    AB-CHMINACA is an indazole-based synthetic cannabinoid. It is a potent agonist of the CB₁ receptor and CB₂ receptor and fully substitutes for Δ⁹-THC in rat discrimination studies, while being 16x more potent

    AB-CHMINACA is an indazole-based synthetic cannabinoid. It is a potent agonist of the CB₁ receptor and CB₂ receptor and fully substitutes for Δ⁹-THC in rat discrimination studies, while being 16x more potent

    AB-CHMINACA is structurally relevant to AB-FUBINACA which includes a cyclohexyl group replaced for the 4-fluorophenyl group. The physical and toxicological attributes associated with the substance haven’t been identified. The product was created for research and forensic purposes.

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