Myrcene

Aroma chemical · Green / Aromatic

herbal, balsamic, green, resinous — top note.

Aroma illustration for Myrcene: a sprig of herbs, drops of golden resin and green leaves, for its herbal, balsamic, resinous and green notes. It illustrates smell associations, not the material or its source.Skeletal formula of Myrcene (beta-Myrcene), C10H16, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Myrcene smells like (herbal, balsamic, resinous, green), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 31253). Stereochemistry is not shown; the coloured background is decoration.
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By the RUŌOD Lab TeamRevision 1Updated

In short

Myrcene is an acyclic monoterpene found in hops, bay, lemongrass and many other oils. It has a herbal, balsamic odour and is the starting point for many aroma chemicals.

What Myrcene smells like

Myrcene is a light, volatile terpene with a sweet, balsamic-resinous character. Arctander, as quoted by The Good Scents Company, describes it as refreshing, almost citrusy, but warm-balsamic and ethereal-sweet. Suppliers describe a sweet, balsamic, resinous odour with fruity-green and citrus nuances; Takasago a sweet-balsamic, resinous 'gum' odour of poor tenacity; and others herbaceous and woody notes. It is short-lived — under an hour on a blotter.

Leading note
Sweet balsamic-resinous
Supporting facets
Citrus-like freshness, herbaceous
Faint facets
Fruity-green
Character
Light, sweet, ethereal, fleeting
  • herbal
  • balsamic
  • green
  • resinous

What makes Myrcene distinctive

It is a warm, balsamic terpene rather than a sharp one: refreshing and almost citrusy like the citrus terpenes, but with a resinous, gum-like sweetness. It is the main volatile of hop oil.

Where the descriptions disagree: A metallic note appears only in one consumer glossary; supplier and reference descriptions do not mention it.

How Myrcene is used

Used for a fresh, spicy-refreshing lift in citrus and spice colognes, as Arctander notes, and as a starting material for other fragrance chemicals. Its poor tenacity limits it to the top note.

Typical role: modifier (used in small amounts to change the character of a blend).

How Myrcene differs from similar materials

beta-Ocimene
Beta-ocimene is warmer, more floral and herbaceous; myrcene is more balsamic-resinous and citrus-fresh.
Hop Oil
Myrcene is the dominant constituent of hop oil; the oil adds the spicy, woody humulene and caryophyllene notes that make it 'hoppy'.
Juniper Berry Oil
Juniper berry owes part of its peppery warmth to myrcene, inside a sparkling, terpenic, gin-like berry. (compared directly by a cited source)

An asterisk marks a difference that a cited source states directly. The others compare the published descriptions of each material. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

Polymerises and oxidises readily; store cold and use fresh.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Green / Aromatic
Note position
Top note
Physical form at room temperature
Liquid
Also known as
beta-Myrcene, 7-Methyl-3-methyleneocta-1,6-diene
CAS number
123-35-3
Molecular formula
C10H16
Molecular weight
136.23 g/mol
IUPAC name
7-methyl-3-methylideneocta-1,6-diene

The CAS number, formula and molecular weight are taken from PubChem compound 31253, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. Companies notifying the ECHA C&L Inventory classify it (2,180 reports): H226 flammable liquid and vapor (99.8% of reports); H304 may be fatal if swallowed and enters airways (99% of reports); H315 causes skin irritation (85.6% of reports); H319 causes serious eye irritation (85.5% of reports); H412 harmful to aquatic life with long lasting effects (18.7% of reports); H400 very toxic to aquatic life (14.6% of reports). Unless it is harmonised, this is the notifiers' own classification, not a binding one.

This page is general information, not a safety assessment or a specification. Confirm identity, composition, IFRA status and allergen content from your supplier's documents for the lot you hold.

Materials it works with

Myrcene is also suggested as a partner on the pages for alpha-Humulene and beta-Ocimene.

Used in formulas and accords

Used in 4 published formulas

Myrcene is an ingredient in 2 accords and 2 bases in the Formula & Accord Library.

Further reading

Questions about Myrcene

Is Myrcene natural or synthetic?

The molecule occurs in nature. Commercial Myrcene may be made by synthesis or obtained from natural sources, so check the supplier's specification if the distinction matters to you.

What is the CAS number of Myrcene?

123-35-3. It was checked against PubChem on 19 October 2026.

Which published formulas use Myrcene?

Myrcene is used in 4 published formulas in the RUŌOD Lab Formula & Accord Library, including Cannabis Base, Fig Accord and Mango Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

Keep your own record of Myrcene — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.