KC 33
Top flavors
Terpenes
KC 33 effects are mostly calming.
KC 33
KC 33 is a modern hybrid strain derived from a Brazilian landrace crossed with a secondary hybrid variety. As a versatile cultivar suitable for both indoor and outdoor cultivation, it reaches maturity after a 53-day flowering period. Growers generally classify the strain as having moderate difficulty, yet it is notable for producing a high yield. Its genetic influence is extensive, serving as a pillar for various offspring including Early Bud, KC 33 x Master Kush, Secret Project Number 1, Spontanica, Sudden Flower, and Tropic Punch.
The aromatic and sensory profile of KC 33 is defined by a complex chemical composition, led by a dominant concentration of nerolidol followed by secondary levels of limonene and caryophyllene. The full terpene spectrum continues with humulene, linalool, myrcene, bisabolol, and beta-pinene, rounded out by trace amounts of caryophyllene-oxide, camphene, terpinolene, and pinene. These compounds combine to provide a distinct profile, moving through nuances of wood and spice underscored by the citrus-forward presence of limonene.
As a THC-dominant variety, KC 33 is primarily utilized for its ability to induce feelings of relaxation, happiness, and an uplifted mood. These therapeutic properties make it a frequent choice for those seeking relief from stress, pain, and sleep-related concerns. Through its wide-ranging genetic reach, the strain remains a significant contributor to modern breeding, establishing a consistent legacy within the cannabis community.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| nerolidol | ~60% | floral | sleep · relaxing |
| limonene | ~28% | citrus | social · creative |
| 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.
Russo 2011: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
~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
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of KC 33.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parent brazil hybrid
Offspring — 5 strains bred from KC 33
Composite Traits
Where to buy KC 33
No verified dispensaries on file — find it on Leafly.
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What would KC 33 × ? 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 KC 33 →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is KC 33 indica or sativa?
KC 33 is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in KC 33?
Nerolidol is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is KC 33 good for daytime use?
KC 33 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.