Auto Kerosene Krash
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Terpenes
Auto Kerosene Krash has balanced effects.
Auto Kerosene Krash
Auto Kerosene Krash is a modern autoflowering variety developed from AutoGlueberry OG. This strain is designed for cultivators seeking an accessible growing experience, as it is classified as easy to manage in both indoor and outdoor environments. Growers should anticipate a flowering cycle of 84 days and a low overall yield. Its genetic lineage distinguishes it as a contemporary cross, distinct from landrace or heirloom varieties.
The terpene profile for Auto Kerosene Krash is complex, led by caryophyllene, myrcene, and limonene. These primary constituents are supported by humulene, linalool, bisabolol, and nerolidol, with further notes of beta-pinene, pinene, geraniol, borneol, camphene, terpinolene, and caryophyllene-oxide. This diverse chemical spectrum structures the sensory experience, balancing pungent, spicy undertones with softer floral and citrus aromatic qualities.
This THC-dominant strain is primarily utilized by consumers seeking relief from stress, pain, and sleep difficulties. Users consistently report effects characterized by a sense of relaxation, happiness, and an uplifted mood. Beyond its utility for individual consumers, the strain has contributed to the development of new genetics, specifically serving as the parent of the Wicked Witch Auto.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| myrcene | ~28% | earthy | relaxing · solo |
| 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.
~60%
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: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
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
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 Auto Kerosene Krash.
Ancestry
Great-great-grandparents
Great-grandparents
Siblings
Share parent autoglueberry og
Offspring — 1 strains bred from Auto Kerosene Krash
Composite Traits
Where to buy Auto Kerosene Krash
No verified dispensaries on file — find it on Leafly.
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What would Auto Kerosene Krash × ? 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 Auto Kerosene Krash indica or sativa?
Auto Kerosene Krash is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto Kerosene Krash?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Auto Kerosene Krash good for daytime use?
Auto Kerosene Krash 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.