59770

Supelco

(−)-Isopulegol

analytical standard

Synonym(s):
(1R,2S,5R)-2-Isopropenyl-5-methylcyclohexanol, (1R,3R,4S)-p-Menth-8-en-3-ol
Empirical Formula (Hill Notation):
C10H18O
CAS Number:
Molecular Weight:
154.25
Beilstein/REAXYS Number:
1906573
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

Quality Level

grade

analytical standard

assay

≥99.0% (sum of enantiomers, GC)

form

neat

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

application(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.)

Featured Industry

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

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General description

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

Application

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

Other Notes

Monoterpenoid chiral building block, hydroboration to a 1,4-diol

pictograms

Exclamation mark

signalword

Warning

hazcat

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

Target Organs

Respiratory system

storage_class_code

10 - Combustible liquids

WGK Germany

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

Certificate of Analysis

Certificate of Origin

G. Schmid et al.
Journal of the American Chemical Society, 105, 624-624 (1983)
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)
C.W. Jefford et al.
Organic Syntheses, 71, 207-207 (1993)
[The metabolic products of microorganisms. Boromycin].
R Hütter et al.
Helvetica chimica acta, 50(6), 1533-1539 (1967-01-01)

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