FRDD

Forensically-Relevant Drug Database

NPS Discover

Description

Preferred Drug Name

THCP

Brief Description

THCP is a semi-synthetic cannabinoid categorized as a phytocannabinoid and is structurally similar to other phytocannabinoids (e.g., THC, CBD, CBDP). THCP is present at trace amounts in Cannabis sativa; however, drug products purportedly containing synthetically derived THCP have been sold online and in smoke shops in the form of plant materials, edibles, and vapes. THCP was first identified by our laboratory in May 2025 and confirmed after acquiring standard reference material.

Structure


Nomenclature

Formal Name (IUPAC)

3-heptyl-6,6,9-trimethyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol

Synonyms

Δ9-Tetrahydrocannabiphorol, Δ9-THC-C7, Δ9-THC-heptyl

Identifiers

CAS Numbers

54763-99-4

Chemistry

Chemical Formula

C23H34O2

Molecular Mass

342.50

Molecular Ion

342

Exact Mass

343.2632

SMILES

CC1=C[C@]2([H])[C@@](C(C)(C)OC3=C2C(O)=CC(CCCCCCC)=C3)([H])CC1

InChI String

InChI=1S/C23H34O2/c1-5-6-7-8-9-10-17-14-20(24)22-18-13-16(2)11-12-19(18)23(3,4)25-21(22)15-17/h13-15,18-19,24H,5-12H2,1-4H3/t18-,19-/m1/s1

InChI Key

OJTMRZHYTZMJKX-RTBURBONSA-N

GCMS Analytics

Lab

CFSRE (Willow Grove, PA)

Comments

Sample Preparation:

Drug Materials: Dilution in methanol or acid / base extraction

Drug Standards: Dilution in methanol

Instrument:Agilent 5975 Series GC/MSD System
Column:Agilent J&W DB-1 (12 m x 200 µm x 0.33 µm)
Carrier Gas:Helium (Flow: 1.46 mL/min)
Temperatures:

Injection Port: 265 °C

Transfer Line: 300 °C

MS Source: 230 °C

MS Quad: 150 °C

Oven Program: 50 °C for 0 min, 30 °C/min to 340 °C for 2.3 min

Injection Parameters:Injection Type: Splitless, Injection Volume: 1 µL
MS Parameters:Mass Scan Range: 40-550 m/z

 

Images

Fragments

327
342
259
299
243

HRMS Analytics

Lab

CFSRE (Willow Grove, PA)

Comments

Sample Preparation:

Toxicology Samples: Liquid-liquid extraction

Drug Materials: Dilution of sample in mobile phase

Instrument:

Sciex TripleTOF® 5600+, Shimadzu Nexera XR UHPLC

Sciex X500R, Sciex ExionLC

Column:Phenomenex® Kinetex C18 (50 mm x 3.0 mm, 2.6 µm)
Mobile Phase:

A: Ammonium formate (10 mM, pH 3.0)

B: Methanol/acetonitrile (50:50)

Flow rate: 0.4 mL/min

Gradient:Initial: 95A:5B; 5A:95B over 13 min; 95A:5B at 15.5 min
Temperatures:

Autosampler: 15 °C

Column Oven: 30 °C

Source Heater: 600 °C

Injection Parameters: Injection Volume: 10 µL
QTOF Parameters:

TOF MS Scan Range: 100-510 Da

Precursor Isolation: SWATH® acquisition (27 windows)

Fragmentation: Collison Energy Spread (35±15 eV)

MS/MS Scan Range: 50-510 Da

 

Images

Fragments

343.2621
221.1526
287.1994
135.1167
123.0443

Drug Origins and Uses

Drug Origins and Uses

Illicit, Semi-Synthetic

Biological Effects

Biological Effects

Analgesic, Sedative/Hypnotic

Target Receptor or Neurotransmitter

Target Receptor or Neurotransmitter

CB1

Pharmacodynamics

Pharmacodynamics

Agonist

Toxicology Data Clinical Nonfatal

Source

PCN Reports: Psychiatry and Clinical Neurosciences

Title

Psychosis and suicide attempt following a single use of delta-9-tetrahydrocannabiphorol: A case report

Reference Link


Drug Control

US Controlled Substance Schedule

Schedule I

UN Drug Control Scheduling

1961 Convention: Schedule I


Patent Literature

Source

Google Patents

Title

Catalytic cannabinoid processes and precursors

Reference Link


Pharmacology Literature

Source

Scientific Reports

Title

A novel phytocannabinoid isolated from Cannabis sativa L. with an in vivo cannabimimetic activity higher than Δ9-tetrahydrocannabinol: Δ9-Tetrahydrocannabiphorol

Reference Link


Analytical Literature

Source

Journal of Analytical Toxicology

Title

Determination of Cross-Reactivity of Contemporary Cannabinoids with THC Direct Immunoassay (ELISA) in Whole Blood

Reference Link


Source

Psychoactives

Title

The Identification of Synthetic Impurities in a Vape Pen Containing Δ9-Tetrahydrocannabiphorol Using Gas Chromatography Coupled with Mass Spectrometry

Reference Link


Source

Forensic Chemistry

Title

Δ9-Tetrahydrocannabiphorol: Identification and quantification in recreational products

Reference Link


Published January 27, 2026