Mata Hari
23.2%
THC
0.05%
CBD
Top flavors
Terpenes
Mata Hari effects are mostly energizing.
Mata Hari potency is average.
Mata Hari
23.2%
THC
0.05%
CBD
Top flavors
Terpenes
Mata Hari effects are mostly energizing.
Mata Hari potency is average.
Mata Hari is a modern hybrid-indica cultivar derived from a three-way cross between Calizahr, Alpine Rocket, and Purpurea Ticinensis. Developed as a versatile selection for various environments, this strain requires a moderate level of cultivation skill to reach its potential. Growers can anticipate a high yield from this variety, which reaches maturity after a 60-day flowering period.
The chemical expression of Mata Hari is complex, led by a dominant profile of terpinolene, followed closely by myrcene, pinene, and limonene. Beneath these primary notes, the profile incorporates caryophyllene, ocimene, beta-pinene, and humulene. The sequence continues with subtle contributions from linalool, bisabolol, guaiol, alpha-terpinene, nerolidol, and gamma-terpinene. This broad spectrum of compounds creates a distinct aromatic and flavor experience defined by the specific hierarchy of these fourteen terpenes.
As a THC-dominant strain, Mata Hari is sought after for its ability to induce states of relaxation, calm, and mental focus. These therapeutic qualities make it a frequent choice for the management of pain, stress, and sleep-related concerns. The influence of its genetics extends to its progeny, most notably represented by the offspring variety Red Dawn.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| terpinolene | ~60% | herbal | creative · social |
| myrcene | ~28% | earthy | relaxing · solo |
| pinene | ~12% | pine | focus · creative |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
~60%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
Genetic Profile
Indica-dominant
Primarily indica with sativa influence. Relaxing body with some cerebral lift.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Mata Hari.
Ancestry
Great-great-grandparents
Grandparents
Parents
Siblings
Share parents calizahr / alpine rocket / purpurea ticinensis
Offspring — 1 strains bred from Mata Hari
Composite Traits
Where to buy Mata Hari
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
Find which dispensaries near you currently stock Mata Hari.
or enter a city / postcode
Community Reviews
No reviews yet — be the first!
No reviews yet for Mata Hari.
What would Mata Hari × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
Build a cross with Mata Hari →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Mata Hari indica or sativa?
Mata Hari is modeled here as a indica-dominant (primarily indica with sativa influence).
What terpene is dominant in Mata Hari?
Terpinolene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Mata Hari good for daytime use?
Mata Hari is versatile and works across different times of day depending on dose and individual response.
How accurate is this data?
See the "Data confidence" card in the sidebar. Terpene profiles and effects are chemistry-informed estimates — individual responses depend on phenotype, source, and personal chemistry.