Rhino Krack
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Terpenes
Rhino Krack effects are mostly calming.
Rhino Krack
Rhino Krack is a modern hybrid, established through the crossbreeding of White Rhino, Kaya’s Koffee, and Plum Crazy. This tripartite lineage results in a stable genetic profile that performs effectively across both indoor and outdoor cultivation environments. Growers can expect a high yield from this moderate-difficulty strain, which completes its flowering cycle over a period of 67 days.
The terpene profile of Rhino Krack is a complex sequence starting with myrcene as the primary compound, followed by caryophyllene and limonene. The lesser-represented aromatic nuances include pinene, linalool, beta-pinene, humulene, nerolidol, bisabolol, guaiol, camphene, ocimene, terpinolene, geraniol, and p-cymene. These components combine to dictate the sensory experience of the cultivar, grounding the chemical composition in a diverse range of terpenes that follow this specific order of dominance from primary to tertiary and beyond.
Rhino Krack is a THC-dominant hybrid characterized by its ability to induce effects that are consistently reported as relaxed, happy, and uplifted. These traits make the strain a suitable candidate for users seeking relief from stress, pain, or difficulty with sleep. The genetic legacy of this hybrid is evidenced by its notable offspring, which include Medellin Krack, Subcools Krack, and Unicorn Krack.
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 Rhino Krack.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Parents
Siblings
Share parents white rhino / kayas koffee / plum crazy
Offspring — 3 strains bred from Rhino Krack
Composite Traits
Where to buy Rhino Krack
No verified dispensaries on file — find it on Leafly.
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What would Rhino Krack × ? 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 Rhino Krack indica or sativa?
Rhino Krack is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Rhino Krack?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Rhino Krack good for daytime use?
Rhino Krack 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.