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(+/-)-11-Nor-9-Tetrahydrocannabinol-[d3]

General Information
Catalog: BLP-010137
CAS: 136844-96-7
Molecular Formula: C21H25D3O4
Molecular Weight: 347.46
Chemical Structure
(+/-)-11-Nor-9-Tetrahydrocannabinol-[d3]
Synonyms (6aR,10aR)-rel-6a,7,8,10a-Tetrahydro-1-hydroxy-6,6-dimethyl-3-(pentyl-5,5,5-d3)-6H-dibenzo[b,d]pyran
IUPAC Name 1-hydroxy-6,6-dimethyl-3-(5,5,5-trideuteriopentyl)-6a,7,8,10a-tetrahydrobenzo[c]chromene-9-carboxylic acid
Related CAS 104874-50-2 (unlabelled)
Canonical SMILES CCCCCC1=CC(=C2C3C=C(CCC3C(OC2=C1)(C)C)C(=O)O)O
InChI InChI=1S/C21H28O4/c1-4-5-6-7-13-10-17(22)19-15-12-14(20(23)24)8-9-16(15)21(2,3)25-18(19)11-13/h10-12,15-16,22H,4-9H2,1-3H3,(H,23,24)/i1D3
InChI Key YOVRGSHRZRJTLZ-FIBGUPNXSA-N
Purity >98%
Storage Store at 2-8°C

(+/-)-11-Nor-9-Tetrahydrocannabinol-[d3], a deuterated analog of a primary metabolite of THC, finds diverse applications in scientific and research realms. Delve into key applications of (+/-)-11-Nor-9-Tetrahydrocannabinol-[d3], presented with high perplexity and burstiness:

Analytical Chemistry: This compound serves as a pivotal internal standard for quantifying cannabinoids in biological samples. By furnishing a known reference point, it safeguards the precision and dependability of analytical measurements. Its significance transcends to forensic toxicology and pharmacokinetic inquiries, unraveling THC exposure levels with precision.

Pharmacokinetic Research: (+/-)-11-Nor-9-Tetrahydrocannabinol-[d3] plays a crucial role in exploring the metabolism and elimination of cannabinoids in both human and animal subjects. Researchers trace the compound's dissemination and elimination dynamics, unearthing insights into the biological destiny of cannabinoids. This data is indispensable for deciphering the temporal dimensions of drug effects and implications for drug screening protocols.

Forensic Toxicology: Indispensable in forensic scenarios, this labeled metabolite is paramount for pinpointing and gauging cannabinoid utilization. It facilitates the precise estimation of THC derivatives in diverse biological matrices, such as hair, urine, and blood specimens. This analytical tool stands as a cornerstone in legal and clinical milieus, confirming recent cannabis consumption and evaluating impairment levels.

Drug Development: The exploration of (+/-)-11-Nor-9-Tetrahydrocannabinol-[d3] catalyzes advancements in cannabis-based pharmaceuticals by shedding light on metabolic pathways. A profound comprehension of THC and its analogs' metabolism informs dosage schedules and safety profiles for therapeutic endeavors. This wealth of insights acts as a compass for crafting efficacious and safe cannabinoid-derived therapeutic interventions.

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