THC
Δ9-THC
(−)-trans-Δ9-Tetrahydrocannabinol
Molecular Formula
C21H30O2
Molecular Weight
314.46 g/mol
CAS Number
1972-08-3
Boiling Point
157°C
Overview
THC is the main reason cannabis produces a high. It's the most abundant psychoactive compound in most cannabis products, and when you see a percentage on a dispensary label, that number almost always refers to THC. Everything from the euphoria to the munchies to the occasional anxiety at higher doses traces back to this one molecule. It's been studied more thoroughly than any other cannabinoid, and it's the compound against which every regulated cannabis product is measured.
The Chemistry
THC is fat-soluble, which has two practical effects: it doesn't mix with water (explaining why oil-based formats like edibles and tinctures work), and it stores in body fat for days to weeks (explaining why it shows up on drug tests long after effects have faded). THC also degrades over time into CBN — another cannabinoid — which is why properly stored, fresh cannabis is more potent than old or poorly stored product.
Where It Comes From
THC isn't actually in the cannabis plant as THC — it starts as THCA, the raw acid form. Heat triggers a chemical conversion called decarboxylation, turning non-intoxicating THCA into psychoactive THC. This is why eating raw cannabis doesn't get you high, but smoking, vaping, or cooking with it does. Every time you light a bowl or bite into an edible, decarboxylation either happened in the moment or during production.
How It Works in Your Body
THC activates CB1 receptors in the brain — part of the endocannabinoid system, a built-in network that regulates mood, appetite, pain, memory, and sleep. When THC binds to CB1 receptors in the brain's reward and emotion centers, you get euphoria. In memory areas, short-term recall becomes hazy. In appetite centers, you get the munchies. THC is essentially mimicking signaling molecules your brain already produces — just more powerfully and for longer.
What to Expect
Most people experience euphoria, relaxation, altered time perception, heightened senses, and increased appetite. Effects vary widely by dose, product type, and individual biology. High doses — especially from edibles — can cause anxiety, racing heartbeat, and paranoia. The method of consumption matters enormously:
- Inhaled (flower, vape): Onset in minutes, peak at 15–30 minutes, lasts 1–3 hours
- Edibles and capsules: Onset 30–90 minutes, peak at 2–3 hours, lasts 4–8 hours
- Tinctures (under the tongue): Onset 15–45 minutes, lasts 2–4 hours
Tolerance builds quickly with regular use. New consumers should start very low, especially with edibles.
Evidence tier: Clinical (extensive)
In Cannabis Products
THC is on every legal cannabis product label as a percentage. That number is Total THC — calculated as THC + (0.877 × THCA) — the standard for how potent a product is. Products span a wide range:
- Flower and pre-rolls: The THCA/THC percentage shows potency
- Vape cartridges: Often 70–90% THC concentrate
- Edibles (gummies, chocolates, beverages): Dosed in milligrams; 5–10 mg is a standard starting dose
- Tinctures: Dosed in drops; sublingual absorption is faster than swallowing
- Topicals: Applied to skin, don't enter the bloodstream, won't cause a high
Hemp is federally defined as cannabis with ≤0.3% Total THC — why THCA flower sold in hemp markets occupies a legal gray area.
What Research Shows
THC has more clinical research behind it than any other cannabinoid. There is strong evidence for chronic pain relief, reducing chemotherapy-related nausea and vomiting, and easing muscle spasms from multiple sclerosis. A synthetic version called dronabinol (Marinol) has been FDA-approved since 1985 for those uses. Studies on PTSD, sleep disorders, and anxiety show early promise, with ongoing trials.
Chemical Properties
| Molecular Formula | C21H30O2 |
| Molecular Weight | 314.46 g/mol |
| CAS Number | 1972-08-3 |
| Boiling Point | 157°C |
| Solubility | Lipophilic; insoluble in water, soluble in ethanol, chloroform, and oils |
| Stability | Degrades with prolonged exposure to light, heat, and oxygen; converts to CBN over time |
Receptor Activity
| Receptor | Activity |
|---|---|
| CB1 | Partial Agonist |
| CB2 | Partial Agonist |
| Other | GPR55 agonist |
| Other | TRPV1 activator |
| Other | 5-HT3A antagonist |
Known Effects
- Euphoria
- Relaxation
- Altered time perception
- Increased appetite
- Analgesic
- Anti-nausea
- Anxiety (at high doses)
Common Uses
- Pain management
- Nausea and vomiting (chemotherapy)
- Appetite stimulation (HIV/AIDS wasting)
- Sleep aid
- Muscle spasticity (MS)
Regulatory Status (US)
Federally Schedule I in the United States. Legal for adult recreational use in 24+ states and for medical use in most states. Internationally regulated under the 1971 Convention on Psychotropic Substances.
Regulated Industry Relevance
Every legal cannabis product lists Total THC on the label. That number — calculated as THC + (0.877 × THCA) — is the regulated potency metric in every U.S. state market. Product formats range from flower and vapes to edibles and tinctures, each with different onset times and durations.
Research Status
A synthetic form (dronabinol/Marinol) has been FDA-approved since 1985 for nausea and appetite. Strong clinical evidence for chronic pain, chemotherapy-related nausea, and MS spasticity. Active trials for PTSD and sleep.
Sources
- [1]
Gaoni, Y., Mechoulam, R. (1964). Isolation, Structure, and Partial Synthesis of an Active Constituent of Hashish. Journal of the American Chemical Society.
- [2]
Pertwee, R.G. (2008). The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: Δ9-tetrahydrocannabinol, cannabidiol and Δ9-tetrahydrocannabivarin. British Journal of Pharmacology.
- [3]
National Academies of Sciences, Engineering, and Medicine (2017). The Health Effects of Cannabis and Cannabinoids: The Current State of Evidence and Recommendations for Research. National Academies Press.
Last reviewed: 2025-01-01 · Cannabipedia Editorial Team