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89235

Sigma-Aldrich

(−)-Thujopsene

≥97.0% (GC)

Synonym(s):

(1S,6S,10S)-2,2,6,9-Tetramethyltricyclo[8.1.0.01.6]undec-8-ene

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About This Item

Empirical Formula (Hill Notation):
C15H24
CAS Number:
470-40-6
Molecular Weight:
204.35
Beilstein:
1907465
EC Number:
207-426-8
UNSPSC Code:
12352002
PubChem Substance ID:
57653337
NACRES:
NA.22

Assay

≥97.0% (GC)

refractive index

n20/D 1.505

bp

258-260 °C (lit.)

density

0.936 g/mL at 20 °C (lit.)

SMILES string

CC1=CC[C@]2(C)CCCC(C)(C)[C@@]23C[C@@H]13

InChI

1S/C15H24/c1-11-6-9-14(4)8-5-7-13(2,3)15(14)10-12(11)15/h6,12H,5,7-10H2,1-4H3/t12-,14-,15-/m0/s1

InChI key

WXQGPFZDVCRBME-QEJZJMRPSA-N

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °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’.

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Franck A Ditengou et al.
Nature communications, 6, 6279-6279 (2015-02-24)
The mutualistic association of roots with ectomycorrhizal fungi promotes plant health and is a hallmark of boreal and temperate forests worldwide. In the pre-colonization phase, before direct contact, lateral root (LR) production is massively stimulated, yet little is known about

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