Rambutan
21.7%
THC
0.23%
CBG
Top flavors
Terpenes
Rambutan effects are mostly calming.
Rambutan potency is average.
Rambutan
21.7%
THC
0.23%
CBG
Top flavors
Terpenes
Rambutan effects are mostly calming.
Rambutan potency is average.
Rambutan is a modern hybrid-sativa strain developed from Maui Waui genetics. This cultivar is characterized by its balanced yet energetic profile, requiring a 90-day flowering period to complete its cycle. Cultivators will find the strain offers a moderate level of difficulty, with the ability to thrive in both indoor and outdoor environments while producing a high yield of finished flower.
The chemical complexity of Rambutan is anchored by a diverse terpene profile, led by a dominant concentration of myrcene, followed by caryophyllene, limonene, linalool, guaiol, humulene, beta-pinene, nerolidol, caryophyllene-oxide, pinene, valencene, borneol, camphene, ocimene, and eucalyptol. This combination creates a precise sensory experience that differentiates the strain through its layered chemical structure.
As a THC-dominant variety with 21.7% THC and 0.23% CBG, Rambutan is primarily utilized to promote creativity, focus, and social engagement. Users frequently experience effects characterized by a distinct sense of uplift and happiness, making it an appropriate choice for tasks requiring mental clarity or interactive environments. Its influence on the broader cannabis landscape is solidified by its role as a parent strain to Hawaiian Pancakes.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| caryophyllene | ~28% | spicy | relaxing · social |
| limonene | ~12% | citrus | social · creative |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
~28%
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.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
creative
morningAssociated with terpinolene/limonene profiles; dopaminergic and serotonergic modulation via limonene 5-HT1A supports divergent thinking.
uplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
happy
anytimeGenetic Profile
Sativa-dominant
Primarily sativa with indica grounding. Uplifting with body relaxation.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Rambutan.
Siblings
Share parent maui waui
Offspring — 1 strains bred from Rambutan
Composite Traits
Where to buy Rambutan
No verified dispensaries on file — find it on Leafly.
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What would Rambutan × ? 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 Rambutan →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Rambutan indica or sativa?
Rambutan is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Rambutan?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Rambutan good for daytime use?
Rambutan 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.