Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

Safety Information

15598

Supelco

(−)-Borneol

analytical standard

Synonym(s):

endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
464-45-9
Molecular Weight:
154.25
Beilstein:
2038053
EC Number:
207-353-1
MDL number:
MFCD00003759
UNSPSC Code:
85151701
PubChem Substance ID:
329750939
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥99.0% (sum of enantiomers, GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

SMILES string

CC1(C)[C@H]2CC[C@]1(C)[C@H](O)C2

InChI

1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m0/s1

InChI key

DTGKSKDOIYIVQL-QXFUBDJGSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(-)-Borneol is an enantiomer. It is a bicyclic monoterpene compound used gengrally for analgesia and anaesthesia. It is considered as positive modulators of GABA receptors.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H228,H317,H412

Hazard Classifications

Aquatic Chronic 3 - Flam. Sol. 2 - Skin Sens. 1

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 2

Flash Point(F)

150.8 °F

Flash Point(C)

66 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

15598-5G:
15598-BULK:
15598-25G:
15598-1G:
15598-VAR:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH1028
BCCD8856
BCBX2248
BCBR4601V
BCBM2364V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

(−)-Camphor analytical standard

Supelco

21293

(−)-Camphor

(±)-Camphor purum, synthetic, ≥95.0% (GC)

Sigma-Aldrich

21310

(±)-Camphor

(1S)-(−)-Verbenone analytical standard

Supelco

94882

(1S)-(−)-Verbenone

"(+)-And (-)-borneol: efficacious positive modulators of GABA action at human recombinant a 1 ? 2 ? 2L GABA A receptors.
Granger, Renee E., Erica L. Campbell, and Graham AR Johnston.
Biochemical Pharmacology, 69.7, 1101-1111 (2005)
Yang Lu et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 36(16), 2200-2202 (2011-11-22)
To develop a GC-FID method for the determination of borneol concentration in rat plasma and to investigate the pharmacokinetics after injection of novel-Xingnaojing. Novel-Xingnaojing was injected via by caudal vein injection. The blood samples were collected by posterior orbital venous
Na Zhang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 36(22), 3180-3183 (2012-03-02)
To research the content changes of excitatory neurotransmitter and inhibitory neurotransmitter in corpus striatum of rats after single-used borneol and combining it with diazepam in hope of comprehending the activity of borneol on central nervous system and to observe whether
Fatiha El Babili et al.
Journal of medicinal food, 15(7), 671-676 (2012-05-23)
The volatile components from Croton campestris root bark were localized by an anatomical study and analyzed by gas chromatography-mass spectrometry for the first time. The roots of this plant showed secretory cells. These volatile constituents, isolated from the dichloromethane extract
Xiao Song et al.
Die Pharmazie, 67(10), 848-851 (2012-11-10)
The aim of this work was to study the in situ and in vivo nasal absorption of borneol. A novel single pass in situ nasal perfusion technique was applied to examine the rate and extent of nasal absorption of borneol
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service