Skip to Content
Merck
All Photos(1)

Key Documents

59770

Supelco

(−)-Isopulegol

analytical standard

Synonym(s):

(1R,2S,5R)-2-Isopropenyl-5-methylcyclohexanol, (1R,3R,4S)-p-Menth-8-en-3-ol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
Molecular Weight:
154.25
Beilstein:
1906573
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥99.0% (sum of enantiomers, GC)

optical activity

[α]20/D −22±0.5°, neat

optical purity

enantiomeric ratio: ≥99.5:0.5 (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.471 (lit.)
n20/D 1.472

bp

212 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

C[C@@H]1CC[C@H]([C@H](O)C1)C(C)=C

InChI

1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h8-11H,1,4-6H2,2-3H3/t8-,9+,10-/m1/s1

InChI key

ZYTMANIQRDEHIO-KXUCPTDWSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(−)-Isopulegol belongs to the class of terpene compounds occuring in various plant species.

Application

(−)-Isopulegol may be used as an analytical reference standard for the determination of (−)-isopulegol in:
  • Complex commercial sample matrices by gas chromatography coupled to vacuum ultraviolet detector (GC-VUV).
  • Mentha piperita and M. arvensis essential oils by enantioselective GC.
  • Urine samples by high performance liquid chromatography combined with tandem mass spectrometry (HPLC-MS/MS).

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

Other Notes

This compound is commonly found in plants of the genus: mentha
Monoterpenoid chiral building block, hydroboration to a 1,4-diol

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

172.4 °F - closed cup

Flash Point(C)

78 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Human metabolism and excretion kinetics of the fragrance 7-hydroxycitronellal after a single oral or dermal dosage.
Stoeckelhuber M, et al.
International Journal of Hygiene and Environmental Health, 221(2), 239-245 (2018)
Y. Imakura et al.
Journal of the Chemical Society. Chemical Communications, 372-372 (1988)
G. Schmid et al.
Journal of the American Chemical Society, 105, 624-624 (1983)
[The metabolic products of microorganisms. Boromycin].
R Hütter et al.
Helvetica chimica acta, 50(6), 1533-1539 (1967-01-01)
C.W. Jefford et al.
Organic Syntheses, 71, 207-207 (1993)

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