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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
UNSPSC Code:
41116107
NACRES:
NA.22
PubChem Substance ID:
57647964
EC Number:
207-418-4
Beilstein/REAXYS Number:
3196861
MDL number:
MFCD00063003
Assay:
≥95.0% (sum of enantiomers, GC)
Form:
liquid

Key Documents

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InChI key

IRAQOCYXUMOFCW-OSFYFWSMSA-N

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

SMILES string

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

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.)

Quality Level

100

Related Categories

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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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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