BB-22 3-<wbr/>hydroxy<wbr/>quinoline isomer

BB-22 3-hydroxyquinoline isomer

CAT N°: 14505

BB-22 (Item No. 14099) is an analog of the potent synthetic cannabinoid, JWH 018 (Item No. 10900) that is structurally similar to PB-22 (Item No. 14096) and its derivative, 5-fluoro PB-22 (Item No. 14095).{18291,19507} Both BB-22 and PB-22 are distinctive in that an 8-hydroxyquinoline replaces the naphthalene group of JWH 018. BB-22 3-hydroxyquinoline isomer differs from BB-22 structurally by having the hydroxyquinoline group attached at the third carbon instead of through the eighth position of the ring. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.

Territorial Availability: Available through Bertin Technologies only in France

Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.

Special Advice: Please check regulation status before ordering; additionel fees can apply.

  • Synonyms
    • 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid, 3-quinolinyl ester
  • Correlated keywords
    • forensics sciences neurosciences cannabinoids CBs JWHs 018 5-fluoro-PB22 PB-22 isomers CB2 receptors BB22 BBs 22 JWH018 JWH-018 PB22 PB-22 PBs 5-fluoro 8-hydroxyquinoline 8 hydroxyquinolines naphthalenes BB-22 analog potent synthetic structurally similar derivatives replaces groups 3-hydroxyquinoline attached third carbons eighth physiological and toxicological properties research applications analytical references standards QUCHIC
  • Product Overview:
    BB-22 (Item No. 14099) is an analog of the potent synthetic cannabinoid, JWH 018 (Item No. 10900) that is structurally similar to PB-22 (Item No. 14096) and its derivative, 5-fluoro PB-22 (Item No. 14095).{18291,19507} Both BB-22 and PB-22 are distinctive in that an 8-hydroxyquinoline replaces the naphthalene group of JWH 018. BB-22 3-hydroxyquinoline isomer differs from BB-22 structurally by having the hydroxyquinoline group attached at the third carbon instead of through the eighth position of the ring. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.

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