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BB-22 3-carboxyindole metabolite

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    BB-<wbr/>22 3-<wbr/>carboxyindole metabolite
  • BB-<wbr/>22 3-<wbr/>carboxyindole metabolite
Cat No: 14378
Biochemicals - Drugs Of Abuse

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 distinct...


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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.
  • 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid
Correlated keywords:
  • forensics sciences neurosciences cannabinoids CBs JWH 018 5-fluoro-PB22 PB-22 metabolites BB22 BBs 22 BB-22 JWHs 018 JWH-018 JWH018 PB-22 PBs PC22 analogs serum urine potent synthetics derivatives phsychological toxicological toxic research applications 5-flouro 8-hydroxyquinoline carboxyindoles 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-carboxyindole metabolite is expected to be a metabolite of BB-22 that would be detectable both in serum and urine. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
Size 1 mg
Shipping dry ice
CAS Number 858515-71-6
Molecular Formula C16H19NO2
Molecular Weight 257,3
Formulation A crystalline solid
Purity ≥98%
Custom Code 2922.19
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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