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Synthetic aroma chemicals

Borneol

Also known as 2-borneol, Bingpian, Bornyl alcohol

CAS 507-70-0Formula C10H18OMolar mass 154.25 g/molEC 208-080-0
GHS signal word: Danger. Pictograms: Flammable 78 suppliers listed Drug substance
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Borneol chemical structure, C10H18O, CAS 507-70-0
2D chemical structure

Key facts

What buyers check first

All properties
Appearance
White to off-white crystals
Melting point
202 °C
Boiling point
212 °C
Density
Leaves from ligroin, MP 206 °C, BP 213 °C, density: 1.011 g/cm³ at 20 °C. Insoluble in w…
Flash point
60 °C
HS code
290619
Category
Synthetic aroma chemicals
UN number
UN 1312
Illustrative photo, colourless crystals beside a jumbo bulk bag in a chemical plant
Typical packagingIllustrative packaging image, not the actual product

What is Borneol?

Plain description, key identifiers and synonyms

Borneol is a bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. It has a role as a metabolite and a volatile oil component.

Borneol is a borneol and stereoisomers.

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
CAS number
507-70-0Other or deprecated CAS: 10385-78-1, 6627-72-1
EC number
208-080-0
Molecular formula
C10H18O
INCI name
BORNEOL
InChIKey
DTGKSKDOIYIVQL-UHFFFAOYSA-N
InChI
InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3
SMILES (canonical and isomeric)
CC1(C2CCC1(C(C2)O)C)C

Synonyms

  • 2-borneol
  • Bingpian
  • Bornyl alcohol
  • Hechenglongnao
  • Camphol
  • Endo-2-camphanol
  • Borneol, dl-
  • Borneolum syntheticum
  • Sumatra camphor
  • Endo-2-hydroxycamphane
  • DL-Borneol
  • Baros camphor
  • Malayan camphor
  • Bhimsaim camphor
  • 2-Hydroxybornane
  • 2-Camphanol
  • 2-Hydroxycamphane
  • Dryobalanops camphor
  • Endo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
  • 2-endo-Bornyl alcohol
  • Camphane, 2-hydroxy-
  • (+-)-borneol
  • endo-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol
  • 1,7,7-Trimethyl-bicyclo(2.2.1)heptan-2-ol, endo-
  • relief patch
Show all 38 synonyms
  • Soothing patch
  • Healing Cream
  • Tendon Sheath Patch
  • Varicose Veins Patch
  • Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, endo-
  • 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
  • 1,7,7-trimethylnorbornan-2-ol
  • DL-Isoborneol
  • Borneo camphor
  • (+/-)-borneol
  • (+/-)-Isoborneol
  • Borneolum
  • endo-Borneol

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
White to off-white crystalsexp.
Odour
Piney, camphor-like odorexp.
Taste
Burning taste somewhat reminiscent of mintexp.
Melting point
202 °Cexp.
Boiling point
212 °Cexp.
Density
Leaves from ligroin, MP 206 °C, BP 213 °C, density: 1.011 g/cm³ at 20 °C. Insoluble in water, very soluble in ethanol, ether, benzene /Borneol, (+/-)-/exp.
Flash point
60 °Cexp.
Solubility
In water, 738 mg/L at 25 °Cexp.
Vapour pressure
5.02 × 10⁻² mm Hg at 25 °Cexp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
154.25 g/molcalc.
Exact mass
154.1358 Dacalc.
LogP (octanol/water)
2.19calc.
Topological polar surface area
20.23 Ųcalc.
Hydrogen bond donors
1calc.
Hydrogen bond acceptors
1calc.
Rotatable bonds
0calc.
Heavy atoms
11calc.
Rings
2calc.
Aromatic rings
0calc.
Fraction sp3 carbons
1calc.
Formal charge
0calc.
Stereocentres
3calc.
Lipinski rule of five
Passes (0 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Murcko scaffold

The ring system that remains when every side chain is removed

Murcko scaffold of this chemical, C1CC2CCC1C2

C1CC2CCC1C2

2 rings, 7 atoms, the Bicyclo(2.2.1)heptane ring system.

2,580 other chemicals share this scaffold

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Danger
GHS02: Flammable
Flammable
220NFPA 704 rating

Hazard statements

  • H228Flammable solid.
Precautionary statements (5)
  • P210Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
  • P240Ground and bond container and receiving equipment.
  • P241Use explosion-proof electrical, ventilating and lighting equipment.
  • P280Wear protective gloves, protective clothing, eye protection and face protection.
  • P370 + P378In case of fire: Use appropriate media to extinguish.
UN number
UN 1312
Transport hazard class
4.1
Packing group
III

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

Borneol suppliers

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All 78 suppliers
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Where suppliers are based

78 suppliers in 15 countries

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Borneol price

Indicative price range per kg from live supplier offers

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Uses and applications

What the substance is used for, by industry and function

In flavors and fragrances, in the manufacture of its esters.

Borneol is used in the reconstitution of the essential oils in which it occurs naturally.

Used in perfumes for soaps and detergents for woody, camphor, and pine notes.

Traditional medicine.

Industrial uses: Fragrance, Other.

Consumer uses: Fragrance.

Use classes: Cosmetics.

Cosmetic ingredient, INCI name BORNEOL(fragrance, perfuming)

Roles

  • cardiovascular drug
  • eukaryotic metabolite
  • metabolite
  • pharmaceutical
  • plant metabolite
  • volatile oil component

Cosmetic functions

  • Fragrance
  • Perfuming

How it is made

Racemic borneol is prepared synthetically by reduction of camphor or from pinene.

Although borneol is not an herb per se, it is nevertheless a common ingredient in many traditional Chinese herbal formulas. Borneol is actually a compound derived from dryobalanops aromitaca, a tree that belongs to the teak family. The compound is formed by tapping the trunk of the tree, then cooling the substance and allowing it to harden into a clear crystalline substance. Although some borneol is still made by tapping trees, the vast majority of it is created synthetically from turpentine oil or camphor. The compound is ground down into a fine powder before it can be used medicinally.

Regulatory status

Inventories, regulations and trade controls that list this substance

Health and food

  • EU cosmetic ingredient inventory
  • Active ingredient in FDA approved drug labels

United States

  • TSCA inventory (USA)
    Status: Active in US commerce

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code Borneol is traded under.

HS 2906.19Indicative HS code

Cyclanic, cyclenic or cycloterpenic, other

World exports in 2024
$613M
+18.7% vs 2023, imports $606M
2019 to 2024
Top exporters
  1. China34.2%
  2. India * partner reported10.1%
  3. Germany9.5%
Top importers
  1. United States19.8%
  2. Germany9.0%
  3. India * partner reported8.4%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for Borneol is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about Borneol, based on the data on this page

What is Borneol?

Borneol is a bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. It has a role as a metabolite and a volatile oil component.

What is the CAS number of Borneol?

The CAS registry number of Borneol is 507-70-0. Other or deprecated CAS numbers: 10385-78-1, 6627-72-1.

What is the molecular formula and weight of Borneol?

The molecular formula of Borneol is C10H18O and its molar mass is 154.25 g/mol.

What is Borneol used for?

In flavors and fragrances, in the manufacture of its esters. Borneol is used in the reconstitution of the essential oils in which it occurs naturally. Used in perfumes for soaps and detergents for woody, camphor, and pine notes. Traditional medicine. Industrial uses: Fragrance, Other. Consumer uses: Fragrance.

Is Borneol hazardous?

Borneol carries the GHS signal word "Danger". Main hazards: flammable solid. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of Borneol?

Borneol is usually classified under HS code 290619 (Cyclanic, cyclenic or cycloterpenic, other). This is indicative, confirm it with your customs broker before shipping.

Where can I buy Borneol?

CompoundList lists 78 suppliers of Borneol in China, United States, Spain, Hong Kong and 11 more. Send one free request to get and compare quotes. Your contact details stay private until you accept a quote.

What is the price of Borneol?

Suppliers quote Borneol on request because prices depend on grade, purity, quantity and destination. A free request on CompoundList gets you several quotes to compare.

Guides for buyers

Practical guides that help when you source, ship or handle Borneol

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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