Purple Dutch
7.9%
THC
0.01%
CBG
Top flavors
Terpenes
Purple Dutch effects are mostly energizing.
Purple Dutch is lower THC than average.
Purple Dutch
7.9%
THC
0.01%
CBG
Top flavors
Terpenes
Purple Dutch effects are mostly energizing.
Purple Dutch is lower THC than average.
Purple Dutch is a modern, autoflowering variety developed by crossing Purple OG #18 with Ruderalis. Being an autoflowering strain, it is characterized by an efficient 60-day flowering cycle. It is considered easy to cultivate, performing well in both indoor and outdoor environments, though growers should anticipate a low yield.
The chemical profile of Purple Dutch is defined by a complex arrangement of terpenes, led by a dominant presence of terpinolene. This top note is followed by myrcene, caryophyllene, and limonene, with subsequent contributions from pinene, beta-pinene, and ocimene. The remaining aromatic depth is provided by linalool, humulene, nerolidol, and bisabolol, with trace amounts of guaiol, camphene, and isopulegol.
This THC-dominant strain contains approximately 7.9% THC, 0% CBD, and 0.01% CBG. Consumers report that the effects are primarily focused on creating sensations of being relaxed, happy, and uplifted. Its profile makes it a viable candidate for those seeking support for stress, pain, or sleep issues. At this time, there are no recorded instances of notable progeny descending from this specific genetic lineage.
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 |
| caryophyllene | ~12% | spicy | relaxing · social |
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.
~12%
spicy
●●○○
Russo 2011: only terpene that is a selective full CB2 agonist (100 nM); Gertsch et al. 2008: acts as dietary cannabinoid; unique anti-inflammatory and gastric cytoprotective properties.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Autoflower
Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Purple Dutch.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents purple og 18 / ruderalis
Composite Traits
Where to buy Purple Dutch
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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Community Reviews
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What would Purple Dutch × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
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Frequently Asked Questions
Is Purple Dutch indica or sativa?
Purple Dutch is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Purple Dutch?
Terpinolene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Purple Dutch good for daytime use?
Purple Dutch 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.