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D-9-Tetrahydrocannabiphorol (THCP)

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In December 2019, a team of Italian researchers published a paper in Scientific Reports that changed how scientists think about cannabis potency. They had discovered a naturally occurring phytocannabinoid with a seven-carbon side chain — two carbons longer than standard Δ9-THC’s five — and it bound to CB1 receptors with 33 times greater affinity than Δ9-THC in laboratory assays. The compound: delta-9-tetrahydrocannabiphorol (THCP) (Citti et al., 2019).

The discovery immediately triggered both scientific interest and significant consumer hype. Understanding what THCP actually is — and what the “33x stronger” claim does and doesn’t mean — is the purpose of this guide.

What Is THCP?

THCP (Δ9-tetrahydrocannabiphorol) is a naturally occurring phytocannabinoid in Cannabis sativa L. It is a homolog of Δ9-THC in which the standard pentyl (five-carbon) alkyl side chain at the resorcinol ring position is extended to a heptyl (seven-carbon) chain. This two-carbon extension is sufficient to dramatically increase the compound’s fit within the CB1 receptor binding pocket (Citti et al., 2019; Wikipedia contributors, 2025).

THCP was discovered by the same Italian research group (University of Modena and Reggio Emilia) that had previously isolated THC-C4/THCB. They found THCP while conducting detailed mass spectrometry profiling of the FM2 Italian medical cannabis strain. Its natural concentration in cannabis is very low — trace level — meaning it is not a practically significant source of cannabis’s psychoactive effects through normal plant consumption (Citti et al., 2019).

Quick Facts Full name: Δ9-Tetrahydrocannabiphorol (THCP)
Discovered: December 2019 — Citti et al., University of Modena and Reggio Emilia
Published in: Scientific Reports
Side chain: Heptyl (C7) — two carbons longer than Δ9-THC
CB1 receptor Ki: ~1.2 nM (33× greater affinity than Δ9-THC at ~40 nM)
Psychoactive: Yes — full agonist at CB1; more potent than Δ9-THC
Natural abundance: Trace
Legal status: Not internationally scheduled; state laws vary

The 2019 Discovery

The Citti et al. (2019) paper — “A novel phytocannabinoid isolated from Cannabis sativa L. with an in vivo cannabimimetic activity higher than Δ9-tetrahydrocannabinol: Δ9-Tetrahydrocannabiphorol” — was published in Scientific Reports (Nature portfolio). The team isolated THCP from FM2 cannabis, confirmed its structure by stereoselective synthesis and comprehensive spectroscopic methods, and then characterized its pharmacology.

Their key findings: THCP demonstrated CB1 receptor affinity with a Ki of 1.2 nM compared to Δ9-THC’s ~40 nM — approximately a 33-fold difference. In vivo tetrad testing in mice (the standard behavioral assay for CB1 agonism) showed THCP produced “full agonist behavior” at the same 10 mg/kg dose used for Δ9-THC, with cannabimimetic activity described as “far higher” (Citti et al., 2019; ScienceDirect, 2024).

What “33× Greater Binding Affinity” Actually Means

The “33x stronger” figure that dominates THCP marketing requires careful interpretation. The Ki value (1.2 nM vs ~40 nM for Δ9-THC) measures how strongly the compound binds to isolated CB1 receptors in a laboratory assay — not how intense the effect is in a living person. Several factors separate binding affinity from real-world potency:

Binding affinity describes how tightly the molecule fits the receptor. But receptor activation efficiency (efficacy), bioavailability (how much reaches the brain), metabolism rate, and tolerance all determine what someone actually experiences. THCP’s natural concentration in cannabis is trace-level — unlikely to contribute meaningfully to the effects of normal cannabis use. And user reports suggest THCP effects are roughly 5–10× more intense than Δ9-THC in practice — significant, but far below the 33× binding number (Wikipedia contributors, 2025; Canapuff, 2025).

CompoundSide ChainCB1 KiRelative CB1 Affinity
THCV (propyl)C3~75 nM0.5× Δ9-THC
Δ8-THC (pentyl)C5~240 nM~0.2× Δ9-THC
Δ9-THC (pentyl)C5~40 nMReference
THC-C4/THCB (butyl)C415 nM~3× Δ9-THC
THCP (heptyl)C71.2 nM~33× Δ9-THC
High-Potency Safety Warning THCP is significantly more potent than Δ9-THC at CB1 receptors. Consumer THCP products should be approached with extreme caution, especially by those with low THC tolerance. Effects may be unexpectedly intense at doses that would be moderate for standard THC products. Dose responsibly and start at the lowest possible amount.

Frequently Asked Questions

Is THCP 33× stronger than THC?

33× refers to CB1 receptor binding affinity in laboratory assays — not practical potency. In terms of experienced effects, user reports suggest THCP feels roughly 5–10× more intense than standard Δ9-THC, not 33×. Binding affinity is one factor among many that determine a drug’s real-world effect (Citti et al., 2019; Wikipedia contributors, 2025).

Is THCP natural?

Yes — THCP is a naturally occurring phytocannabinoid isolated from cannabis. However, its natural concentration is trace-level (too small to contribute meaningfully to cannabis’s effects from normal use). Consumer THCP products are concentrated or synthetically derived (Citti et al., 2019).

Is THCP legal?

THCP is not internationally scheduled under the Convention on Psychotropic Substances. In the US, its hemp-derived legal status is ambiguous and state-specific. As a structural analogue of Δ9-THC, it may be subject to analogue act provisions in some jurisdictions. Check local laws before purchasing or using THCP products (Recovered.org, 2025).

The Bottom Line

THCP’s discovery in 2019 was a genuine scientific milestone — the first naturally occurring cannabinoid with CB1 binding affinity substantially exceeding that of Δ9-THC, and an important finding for understanding the full pharmacological potential of the cannabis plant. It also raised important questions about cannabis potency: if trace amounts of THCP exist in some strains, they may contribute to the variability in effects that isn’t fully explained by Δ9-THC content alone.

For consumers, THCP products require substantially more caution than standard THC products given their greater potency. The “33× stronger” headline is technically about receptor binding, not subjective experience — but even a practical 5–10× potency multiplier represents a meaningfully higher-risk pharmacological profile than standard cannabis.

Nothing in this article constitutes medical advice. Always consult a qualified healthcare provider before making any decisions about supplementation or treatment.

References

  1. Citti, C., Linciano, P., Russo, F., Luongo, L., Iannotta, M., Maione, S., Laganà, A., Capriotti, A. L., Forni, F., Vandelli, M. A., Gigli, G., & Cannazza, G. (2019). A novel phytocannabinoid isolated from Cannabis sativa L. with an in vivo cannabimimetic activity higher than Δ9-tetrahydrocannabinol: Δ9-Tetrahydrocannabiphorol. Scientific Reports, 9, 20335. https://doi.org/10.1038/s41598-019-56785-1
  2. Canapuff. (2025). THCP vs THC: Is THCP really 33x stronger? Effects, dosing & safety. https://www.canapuff.com/blogs/comparison/thcp-vs-thc
  3. Recovered.org. (2025). Delta-10 THC: Effects, legality, and safety. https://recovered.org/marijuana/delta-10-thc
  4. ScienceDirect. (2024). Δ9-Tetrahydrocannabiphorol: Identification and quantification in recreational products. https://doi.org/10.1016/j.jchromb.2024.124054
  5. Wikipedia contributors. (2025). Tetrahydrocannabiphorol. Wikipedia, The Free Encyclopedia. https://en.wikipedia.org/wiki/Tetrahydrocannabiphorol

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Dale Hewett

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Dale Hewett is the owner and founder of New Phase Blends. He discovered his passion for natural supplements use after suffering from injuries sustained while on Active Duty in the US Army. His number one priority is introducing the same products that he himself uses to others who can benefit from them.

Dale holds a Master Degree of Science, and is the inventor of the popular, CBD-based sleep aid known as ‘Sleep.’ He’s given multiple lectures on CBD and other supplements to institutions such as Cornell’s MBA student program, and Wharton’s School of Business.

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