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Terpene Atlas · Sesquiterpene alcohol

/bih-SAB-oh-lol/ · (-)-α-Bisabolol (levomenol)

Alpha-Bisabolol

The soft chamomile-and-honey sesquiterpene alcohol · genuinely a recognized skin-care ingredient, which lore then over-reads as an internal calming cure.

ChamomileHoneySoft flowersApplesWoodMild pepper
Formula
C₁₅H₂₆O
Weight
222.37 g/mol
Class
C15 · monocyclic (one ring, one hydroxyl)
Form
Clear and colorless to pale yellow

Meet the molecule

One open chain, not a cage

Molecular class
Sesquiterpene alcohol · C15 · monocyclic (one ring, one hydroxyl)
Formula · weight
C₁₅H₂₆O · 222.37 g/mol
Biosynthetic origin
A monocyclic C15 sesquiterpene alcohol derived from farnesyl diphosphate (FPP).
Structural trait
A six-membered ring with a long hydroxyl-tipped side chain · heavy, oily, and slow to evaporate, the opposite of a light monoterpene top note.

Usually reported as α-bisabolol; the natural (-)-levomenol form is the one most sourced from chamomile and candeia.

Aroma spectrum

A qualitative sensory map

Relative prominence is illustrative, not a measured profile. Aroma is never produced by one molecule alone.

floral fruity woody spice

Physical identity

The isolated compound

Appearance
Clear and colorless to pale yellow.
Texture
Viscous oily liquid.
Volatility
A heavy, low-volatility sesquiterpene alcohol · it lingers as a soft base note long after lighter terpenes have gone.

This describes the isolated chemical. It does not predict whether flower will be dense, sticky, purple, or frosty.

Extreme close-up of the Alpha-Bisabolol resin, its glassy interior in detail The resin, up close

Where it appears in nature

Beyond cannabis

Botanical sources of Alpha-Bisabolol: German chamomile, Candeia, Sage, Poplar
German chamomile A primary natural source. Candeia Brazilian candeia trees. Sage Poplar

grams per mole

222.37

A heavy C15 sesquiterpene alcohol · far heavier and slower to evaporate than the light monoterpenes, which is why it lingers as a soft, skin-friendly base note. PubChem

Evidence ladder

What's known · and how well

Research is ranked by strength, not promised as effects. Isolated-compound findings are separated from whole-cannabis evidence throughout.

Established mechanism1 claim

Bisabolol is a monocyclic C15 sesquiterpene alcohol derived from farnesyl diphosphate · established chemistry.

established isolated terpene PubChem PMC
Brain research1 claim

Preclinical sedative, anxiety-modulating, neuroprotective, and analgesic effects have been reported for isolated bisabolol.

animal isolated terpene reference
Preclinical, isolated-compound findings; not demonstrated for a cannabis product in humans.
Body research1 claim

Anti-inflammatory, skin-soothing, antimicrobial, gastroprotective, and wound-healing activity is under investigation for isolated bisabolol.

animal isolated terpene reference
Under investigation; much is preclinical and topical, not internal cannabis-product evidence.
Recognized non-cannabis use1 claim

Widely incorporated into topical products for sensitive or irritated skin · cosmetics, baby products, after-sun, and dermatologic formulations.

approved use non-cannabis product reference
Unproven / insufficient1 claim

No approved internal treatment exists. Its recognized use is topical skin care, not an internal medicine.

unproven isolated terpene reference

Myth vs evidence

The topical-to-internal leap

The claim

Bisabolol really is a recognized skin-soother in cosmetics, so lore assumes a bisabolol-rich product must calm you from the inside too. That leap is not earned.

The evidence

Bisabolol’s skin-soothing use in topical products is recognized. That a bisabolol-containing cannabis product calms or heals you internally is not established · topical evidence is not internal evidence.

unprovenwhole cannabisreference

Where it sits

Alpha-Bisabolol against the field

Objective chemistry and how often it shows up · not effects. Every authored terpene is plotted on each track; Alpha-Bisabolol is lit, the rest stay faint. The picture fills in as the Atlas grows (10 plotted so far).

Dominant aroma family

Its strongest sensory class, brightest to deepest.

Prevalence in cannabis

How often it leads a profile. Qualitative, not measured.

Volatility · boiling point

Lower boils off sooner, reading as an earlier top note.

Molecular weight

C10 monoterpenes are lighter than the C15 sesquiterpenes.

Read as a table
TerpeneDominant aroma familyPrevalence in cannabisVolatility · boiling pointMolecular weight
Myrcene Earthyvery common167 °C136 g/mol
Limonene Citrusvery common176 °C136 g/mol
Pinene Pinecommon155 °C136 g/mol
Linalool Floralcommon198 °C154 g/mol
Beta-Caryophyllene Spicevery common262 °C204 g/mol
Alpha-Humulene Herbalmoderate270 °C204 g/mol
Terpinolene Freshmoderate186 °C136 g/mol
Ocimene Fruityuncommon177 °C136 g/mol
Alpha-Bisabolol this page Floraluncommon314 °C222 g/mol
Nerolidol Woodyuncommon276 °C222 g/mol

Prevalence is a qualitative ordinal, not a measured concentration. Boiling points are approximate atmospheric-pressure values; the heavier sesquiterpenes are usually distilled under vacuum, so those figures are extrapolated.

Terpene neighborhood

Sensory & structural relatives

Nerolidol A fellow sesquiterpene alcohol with a soft, floral character. α-Bisabolene Its hydrocarbon relative. β-Bisabolene A close structural relative.

On a certificate of analysis

How it shows up on a COA

Name variants a lab may print
Bisabolol · α-Bisabolol · alpha-Bisabolol · Levomenol
Isomer note
Panels list ‘bisabolol’; the natural (-)-levomenol form is most common.
Reading it
Reported as a percentage of product mass; absence from a panel can reflect the lab’s method or detection limit, not true absence. Batch values swing widely.

A terpene’s absence from a panel can reflect the panel’s method or detection limit · not true absence. Values swing batch to batch.

In products

Commonly reported · never guaranteed

Soft, chamomile-leaning chemovars

strainCommonly reported with bisabolol present · but a strain name does not guarantee the profile across growers, harvests, or batches.

Safety & handling

Read this before you trust a label

Pure terpene isolates are concentrated industrial chemicals · not the trace amounts in flower. Do not ingest undiluted isolates or apply them to skin without an appropriate dilution.

safety non-cannabis product reference

A product’s terpene panel cannot reliably predict an individual’s response or calm. Cannabinoid dose, route, tolerance, other medications, and personal biology usually matter more.

safety whole cannabis reference

Bisabolol and its oxides both contribute to chamomile’s softness; heat and air shift the balance between them over time.

established isolated terpene reference
THC and other cannabinoids usually influence intoxication more than any single terpene.
A terpene panel cannot reliably predict an individual patient’s response.
Pure isolates are concentrated industrial chemicals · not the trace amounts in flower.
Oxidation, heat, storage, and processing alter terpene chemistry.
Strain names do not guarantee a stable terpene profile across growers, harvests, or batches.
Discuss any cannabis decision, and other medications, with a qualified clinician.

Explore

Alpha-Bisabolol, three ways

Same molecule, three lenses. The information is identical in every mode.

Keep exploring

Where to next

Sources (3)

Last reviewed 2026-07-22 · TerpAlerts editorial

Educational information only · not medical advice, and not a claim that any cannabis product treats, cures, or prevents any condition. Evidence labels describe the strength and scope of research on the isolated compound. See the full site disclaimer and Privacy Policy.