DDhybrid-indica
Hybrid-IndicaModernTHC-Dominantevening

Double Dalai

Top flavors

earthyherbalspicy
CalmingEnergizing

Double Dalai effects are mostly calming.

Double Dalai is a modern hybrid-indica cultivar derived from a complex lineage of Purple Pakistani Chitral, Burmese, and Hindu Kush. Developed as a high-yielding genetic project, this strain maintains a moderate cultivation difficulty and is suitable for both indoor and outdoor environments. Growers can expect a flowering period of approximately 60 days, during which the plant expresses its hybrid traits consistently. Its genetic influence is foundational to several notable offspring, including Chilake x Double Dalai, Dalai Crisp, Dalai Freeze, Double Dalai F3, and Purple Pono.

The sensory profile of Double Dalai is defined by a cascading terpene expression, led by myrcene, terpinolene, and caryophyllene. This initial aromatic presence is balanced by subsequent notes of pinene, limonene, and beta-pinene, while the deeper complexity is rounded out by ocimene, humulene, linalool, nerolidol, and guaiol. The final finish of the profile includes traces of bisabolol, alpha-terpinene, and gamma-terpinene, creating a nuanced chemical structure that distinguishes the strain.

As a THC-dominant variety, Double Dalai is sought after for its specific physiological impact, which is characterized by a relaxed, calm, and focused state. These effects make the strain a functional choice for addressing pain, stress, and sleep concerns. The combination of its potent cannabinoid profile and its diverse secondary metabolite expression has cemented its utility both for medicinal users and as a stable parent for subsequent breeding lines.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

myrcene ~60%terpinolene ~28%caryophyllene ~12%
TerpeneShare
myrcene~60%
terpinolene~28%
caryophyllene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

earthy

●●●○

Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.

~28%

herbal

●○○○

PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.

~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.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

Primarily indica with sativa influence. Relaxing body with some cerebral lift.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Double Dalai.

Ancestry

Double DalaiFull tree →

Offspring — 1 strains bred from Double Dalai

View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-use

Dispensary Locator

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What would Double Dalai × ? 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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Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Double Dalai indica or sativa?

Double Dalai is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Double Dalai?

Myrcene is shown as the dominant terpene at approximately ~60%. Terpinolene follows as the secondary terpene.

Is Double Dalai good for daytime use?

Double Dalai 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.