Double K.C.
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Terpenes
Double K.C. effects are mostly calming.
Double K.C.
Double K.C. is a modern hybrid that serves as a pivotal point in a specific lineage, being both a descendant and a progenitor within a lineage that includes Swiss-xT and Mr. Swiss. This plant is the result of crossing Indica and Sativa genetics, a breeding project that has produced a stable variety suitable for cultivation in both indoor and outdoor environments. Growers can expect a high yield from this strain, which requires a moderate level of expertise and a flowering period of exactly 63 days to reach maturity.
The aromatic and flavor profile of Double K.C. is defined by a specific chemical hierarchy, led by dominant myrcene, followed by secondary caryophyllene and tertiary limonene. This combination shapes the sensory experience, providing a distinct profile that reflects its modern genetic composition. These terpenes work in concert to establish the botanical identity of the strain, grounding the user in a profile that prioritizes earthy, spicy, and citrus-adjacent notes as determined by its verified chemical testing.
In terms of efficacy, Double K.C. is a THC-dominant cultivar known to induce feelings of being relaxed, happy, and uplifted. These effects make it a frequent choice for those seeking relief from stress and pain, or aid for those struggling with sleep. Beyond its immediate user benefits, the strain occupies a notable position in modern breeding, having directly contributed to the development of offspring such as Swiss-xT and Mr. Swiss.
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.
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 Double K.C..
Ancestry
Parents
Siblings
Share parents indica sativa / swiss xt / mr swiss
Offspring — 2 strains bred from Double K.C.
Composite Traits
Where to buy Double K.C.
No verified dispensaries on file — find it on Leafly.
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What would Double K.C. × ? 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 Double K.C. indica or sativa?
Double K.C. is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Double K.C.?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Double K.C. good for daytime use?
Double K.C. 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.