ChemicalBook > CAS DataBase List > (+)-BORNEOL

(+)-BORNEOL

Product Name
(+)-BORNEOL
CAS No.
464-43-7
Chemical Name
(+)-BORNEOL
Synonyms
(1R,2S,4R)-borneol;420247-1G;(+)-Borneol;Borneol（Chp);D-(+)-BORNEOL;Asparagus Root;dextro-borneol;(+)-BORNEOL 98%;(+)-Borneol 97%;d-Bornyl alcohol
CBNumber
CB5184253
Molecular Formula
C10H18O
Formula Weight
154.25
MOL File
464-43-7.mol
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(+)-BORNEOL Property

Melting point:
206-209 °C (lit.)
alpha 
36 º (C=5 IN ETOH)
Boiling point:
237.64°C (rough estimate)
Density 
0.8704 (rough estimate)
refractive index 
1.4723 (estimate)
FEMA 
2157 | BORNEOL
Flash point:
150 °F
storage temp. 
2-8°C
solubility 
DMF: 25 mg/ml; DMF:PBS(pH7.2) (1:2): 0.33 mg/ml; DMSO: 16 mg/ml; Ethanol: 16 mg/ml
pka
15.36±0.60(Predicted)
form 
solid
Odor
at 10.00 % in dipropylene glycol. pine camphor earthy
Odor Type
balsamic
optical activity
[α]20/D 37.0±2.0°, c = 5 in ethanol
Water Solubility 
0.74g/L(25 ºC)
BRN 
2038056
LogP
2.850
CAS DataBase Reference
464-43-7(CAS DataBase Reference)
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Safety

Hazard Codes 
F,Xn
Risk Statements 
11-20/21/22
Safety Statements 
16-33-36-7/9
RIDADR 
UN 1312 4.1/PG 3
WGK Germany 
3
RTECS 
ED7060000
HazardClass 
4.1
PackingGroup 
III
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H228Flammable solid

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
CRM40901
Product name
(+)-Borneol solution
Purity
certifiedreferencematerial,2000?μg/mLinmethanol,ampuleof1?mL
Packaging
1mL
Price
$140
Updated
2025/07/31
Sigma-Aldrich
Product number
68878
Product name
(+)-Borneol
Purity
analytical standard
Packaging
10mg
Price
$315
Updated
2025/07/31
Sigma-Aldrich
Product number
420247
Product name
(+)-Borneol
Purity
97%
Packaging
1g
Price
$196
Updated
2025/07/31
TCI Chemical
Product number
B6417
Product name
(+)-Borneol
Purity
min. 95.0 %
Packaging
1G
Price
$48
Updated
2025/07/31
TCI Chemical
Product number
B6417
Product name
(+)-Borneol
Purity
min. 95.0 %
Packaging
5G
Price
$143
Updated
2025/07/31
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(+)-BORNEOL Chemical Properties,Usage,Production

Chemical Properties

Almost insoluble in water, poorly soluble in Propylene glycol, very soluble in alcohol, miscible with most perfume oils. Dry-camphoraceous, woody-peppery odor. The dryness is characteristic and constitutes the main difference from the odor of isoBorneol. The odor of Borneol is often compared to that of a good grade Rosemary oil (in which Borneol is present).

Uses

(+)-Borneol has been used to study its antiapoptotic, antioxidative and neuroprotective effect in human neuroblastoma cells (SH-SY5Y).

Application

(+)-Borneol has a woody, somewhat minty and slightly burning taste. 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 tyDes of Room-freshener fragrance, Pine odors, etc.

Production Methods

Reduction of D-(+)-camphor with lithium aluminum hydride to a isomeric mixture of (+)-borneol and (-)-isoborneol.

Definition

ChEBI: (+)-borneol is a borneol. It is an enantiomer of a (-)-borneol.

General Description

(+)-Borneol, a bicyclic monoterpene, is found in the essential oils of medicinal plants and is commonly used in traditional Chinese medicine for analgesia and anaesthesia.

Anticancer Research

Wild asparagus root is known as “tian men dong” in traditional Chinese medicine. Itis used to relieve asthma, suppress coughing, and promote expectoration (Huang1998). It is held to be sweet and bitter in flavour and cold in nature, nourishing thelungs and moistening dryness (McNamara and Song 1995). Though studies conductedon asparagus root to examine its biological effects have only been conductedon animals, the evidence so far shows anticancer activity against leukaemia and lungcancer by means of the inhibition of tumour necrosis factor alpha (Huang et al. 2008).

Purification Methods

It can be steam distilled, the distillate is extracted into Et2O, the extract dried with Drierite and evaporated. The residue is then recrystallised from boiling EtOH (charcoal) or pet ether. [Clark & Read J Chem Soc 1773 1934, Beilstein 6 III 295, 6 IV 281.]

(+)-BORNEOL Preparation Products And Raw materials

Raw materials

Preparation Products

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(+)-BORNEOL Suppliers

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View Lastest Price from (+)-BORNEOL manufacturers

Shaanxi Dideu New Materials Co. Ltd
Product
(+)-BORNEOL 464-43-7
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1000kg
Release date
2025-06-19
Hebei Zhanyao Biotechnology Co. Ltd
Product
(+)-BORNEOL 464-43-7
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20 tons
Release date
2021-10-15
Hebei Lvyang Biotechnology Co.,Ltd
Product
Natural borneol 464-43-7
Price
US $150.00/KG
Min. Order
1KG
Purity
99
Supply Ability
20ton
Release date
2021-03-29

464-43-7, (+)-BORNEOLRelated Search:

N-Benzyl-2-norbornanamine Bornyl acetate Carbic anhydride 5-Norbornene-2-carboxamide N-Hydroxy-5-norbornene-2,3-dicarboximide 2-Hydroxyethyl 5-norbornene-2-carboxylate 2-METHYLISOBORNEOL N,N-Diethyl-endo-2-aminonorbornane 5-VINYL-2-NORBORNENE DL-Isoborneol Borneol endo-2-Acetylbicyclo[2.2.1]hept-5-ene Isobornyl isobutyrate (R)-(+)-BORNYLAMINE ENDO-NORBORNEOL Isobornyl acrylate 5-Norbornene-2,3-dicarboxylic acid L(-)-Borneol

  • (+)-Borneol
  • (+)-Borneol,endo-(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
  • (1r,2s,4r)-(+)-borneo
  • (1r-endo)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol
  • 7,7-trimethyl-(1r-endo)-bicyclo(2.2.1)heptan-2-o
  • (+)-BORNEOL 98%
  • (1R)-(+)-BORNEOL (+)-BORNEOL
  • (1R)-endo-Borneol
  • [1R,2S,4R,(+)]-1,7,7-Trimethylbicyclo[2.2.1]heptan2-ol
  • d-Bornyl alcohol
  • ENDO-(1R)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-OL
  • (1R,2S,4R)-borneol
  • Asparagus Root
  • D-(+)-BORNEOL
  • Bicyclo2.2.1heptan-2-ol, 1,7,7-trimethyl-, (1R,2S,4R)-
  • (+)-Borneol (d-Borneol)
  • (+)-BORNEOL USP/EP/BP
  • (+)-Borneol 97%
  • dextro-borneol
  • tianfu-chem_(+)-BORNEOL,464-43-7
  • Borneol（Chp)
  • Dexborneol Concentrated
  • (+)-BORNEOL, 10 mM in DMSO
  • (+)-(1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
  • 420247-1G
  • 464-43-7
  • Asymmetric Synthesis
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