Skip to Content
Merck
All Photos(1)

Key Documents

58924

Sigma-Aldrich

(−)-Isolongifolene

≥98.0% (sum of enantiomers, GC)

Synonym(s):

(1R)-2,2,7,7-Tetramethyltricyclo[6.2.1.01.6]undec-5-ene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C15H24
CAS Number:
Molecular Weight:
204.35
Beilstein:
2207559
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98.0% (sum of enantiomers, GC)

optical activity

[α]20/D −138±2°, c = 1% in ethanol

refractive index

n20/D 1.499

bp

255-256 °C

density

0.930 g/mL at 20 °C (lit.)

SMILES string

CC1(C)CCC=C2C(C)(C)[C@H]3CC[C@@]12C3

InChI

1S/C15H24/c1-13(2)8-5-6-12-14(3,4)11-7-9-15(12,13)10-11/h6,11H,5,7-10H2,1-4H3/t11-,15-/m0/s1

InChI key

CQUAYTJDLQBXCQ-NHYWBVRUSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(-)-Isolongifolene is a sesquiterpene that can be found in pine cone and Japanese cedar essential oils.

Application

(-)-Isolongifolene may be used in the preparation of (-)-isolongifolenone, a potent insect repellent.

Other Notes

This (-)-isolongifolene has an enantiomeric purity of 93%; it is thus the highest purity material ever offered commercially; the double bond can be epoxidized

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

120.2 °F - closed cup

Flash Point(C)

49 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Isolongifolenone: a novel sesquiterpene repellent of ticks and mosquitoes.
Zhang A, et al.
Journal of Medical Entomology, 46(1), 100-106 (2009)
R. Ranganathan et al.
Tetrahedron, 26, 621-621 (1970)
Rienaecker, R. and Graefe, J
Angewandte Chemie (International Edition in English), 97, 348-348 (1985)
Suppression of SOS-inducing activity of chemical mutagens by metabolites from microbial transformation of (-)-isolongifolene.
Sakata K, et al.
Journal of Agricultural and Food Chemistry, 58(4), 2164-2167 (2010)

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