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DEXTRO-BORNEOL

CAS
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EC
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Material type
synthetic aroma chemical
Canonical source
arctander
Formulation

Usage guidance

Suggested min
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Suggested max
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Cost
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Stock
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Compatibility tags
fougerepine-accordincenseherbalaromaticchypre
How it behaves

Olfactory profile

Family
herbal
Note tendency
Middle
Descriptors
woodyherbaceousmintycamphoraceouspine

Sharp, cool camphoraceous odor with a piney-woody character and a faint peppery-mint facet. Drier and more resinous than levo-borneol, with a clean terpenic freshness that fades to a soft woody-earthy undertone.AI · claude-opus-4-7

Intensity
7 / 10
Tenacity
5 / 10
Volatility
7 / 10
Members

The rest of this material

Composition, IFRA restriction figures, allergen concentrations and where this material is bought are part of Perfume Foundry’s curated library and need an account. Create one or sign in.

chemicals · No. 350

Arctander monograph

Perfume and Flavor Chemicals, page 153.

BASEtenacity · moderatepower · moderateG.R.A.S.FEMA 2157
drycamphoraceouswoodypepperymintyburning
MW
154.25
BP
214°C
MP
204°C
Sp.Gr.
1.01
Refractive n
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Rotation
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Appearance

Hexagonal plates or leaflets.

Solubility

Almost insoluble in water, poorly soluble in propylene glycol, very soluble in alcohol, miscible with most perfume oils.

Odor

Dry-camphoraceous, woody-peppery odor. The dryness is characteristic and constitutes the main difference from the odor of iso-Borneol. The odor of Borneol is often compared to that of a good grade Rosemary oil (in which Borneol is present).

Flavor

Borneol has a woody, somewhat minty and slightly burning taste.

Uses in perfumery

This alcohol blends excellently with Olibanum products for incense type fragrances, and it forms a good background in many herbaceous-camphoraceous fragrances, Lavender- and Citrus cologne types, many types of room-freshener fragrance, Pine odors, etc.

Uses in flavor

Borneol is used in Nut and Spice flavor compositions, usually in mere traces.

Production

Produced by sodium-reduction of d-Camphor. This yields a mixture of d-Borneol and iso-Borneol, or by MPV reduction of Camphor. Yields 50/50 mixture of above, or from Pinene via Pinene hydrochloride to Bornyl acetate to Borneol. Purification by dehydration to which Borneol is resistant.

Identity
Aliases · 7
1,7,7-Trimethyl bicyclo[2.2.1]heptanol-22-Camphanol2-Hydroxy bornane2-Hydroxy camphaneBorneo camphorBornyl alcohold-Camphanol
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).