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Sigma-Aldrich

(−)-α-Cedrene

≥95.0% (sum of enantiomers, GC)

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Synonym(s):
(1S,2R,5S)-2,6,6,8-Tetramethyltricyclo[5.3.1.01.5]undec-8-ene
Empirical Formula (Hill Notation):
C15H24
CAS Number:
469-61-4
Molecular Weight:
204.35
Beilstein:
3196861
EC Number:
207-418-4
MDL number:
MFCD00063003
UNSPSC Code:
12352200
PubChem Substance ID:
57647964
NACRES:
NA.22

Quality Level

100

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

Related Categories

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H400

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

219.2 °F

Flash Point(C)

104 °C

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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