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Key Documents

22133

Sigma-Aldrich

(−)-α-Cedrene

≥95.0% (sum of enantiomers, GC)

Synonym(s):

(1S,2R,5S)-2,6,6,8-Tetramethyltricyclo[5.3.1.01.5]undec-8-ene

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About This Item

Empirical Formula (Hill Notation):
C15H24
CAS Number:
Molecular Weight:
204.35
Beilstein:
3196861
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.22

Assay

≥95.0% (sum of enantiomers, GC)

form

liquid

optical activity

[α]20/D −88±1°, c = 10% in ethanol

refractive index

n20/D 1.498

bp

261-262 °C (lit.)

density

0.932 g/mL at 20 °C (lit.)

SMILES string

C[C@@H]1CC[C@H]2C(C)(C)[C@H]3C[C@@]12CC=C3C

InChI

1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12+,13+,15+/m1/s1

InChI key

IRAQOCYXUMOFCW-OSFYFWSMSA-N

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2

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)

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Zuodong Jiang et al.
Current protocols in plant biology, 1, 345-358 (2016-11-22)
Terpenes/terpenoids constitute one of the largest classes of natural products, this is due to the incredible chemical diversity that can arise from the biochemical transformations of the relatively simple prenyl diphosphate starter units. All terpenes/terpenoids comprise a hydrocarbon backbone that

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