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Merck
CN

22133

(−)-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:
469-61-4
Molecular Weight:
204.35
Beilstein:
3196861
EC Number:
207-418-4
MDL number:
MFCD00063003
UNSPSC Code:
41116107
PubChem Substance ID:
57647964
NACRES:
NA.22

Key Documents

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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

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF6862
BCCD2041
BCBW8101
BCBQ3188V
BCBT5516

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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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