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(+)-β-Cedrene - ≥95.0% (sum of enantiomers, GC), high purity , CAS No.546-28-1

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(+)-β-Cedrene - ≥95.0% (sum of enantiomers, GC), high purity , CAS No.546-28-1

5 Citations

COA

Grade & Purity:

≥95%(GC)
sum of enantiomers

Cas Number: 546-28-1
Molecular Weight: 204.35
MDL number: MFCD00043428
PubChem CID: 11106485

In stock

Item Number

C464126

Grouped product items
SKU	Size	Availability	Price	Qty
C464126-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$598.90

View related series

Fungal (844)

Basic Description

Synonyms	EINECS 208-898-8 \| (+)-beta-Funebrene \| beta-Cedrene \| 1H-3A,7-METHANOAZULENE, OCTAHYDRO-3,8,8-TRIMETHYL-6-METHYLENE-, (3R-(3.ALPHA.,3A.BETA.,7.BETA.,8A.ALPHA.))- \| 1H-3a,7-Methanoazulene, octahydro-3,8,8-trimethyl-6-methylene-, [3R-(3.alpha.,3a.beta.,7.b
Specifications & Purity	≥95%(GC), sum of enantiomers
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Description β-Cedrene is a tricyclic sesquiterpene obtained fromJuniperus cedrusandJuniperus thurifera. It is the main constituent of cedarwood oil, which is used as a raw material for biofuel development.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Sesquiterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Sesquiterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Cedrane and isocedrane sesquiterpenoids
Alternative Parents	Polycyclic hydrocarbons Branched unsaturated hydrocarbons Cyclic olefins Unsaturated aliphatic hydrocarbons
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Cedrane sesquiterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as cedrane and isocedrane sesquiterpenoids. These are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane
INCHI	InChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h11-13H,1,5-9H2,2-4H3/t11-,12+,13+,15+/m1/s1
InChIKey	DYLPEFGBWGEFBB-OSFYFWSMSA-N
Smiles	CC1CCC2C13CCC(=C)C(C3)C2(C)C
Isomeric SMILES	C[C@@H]1CC[C@@H]2[C@]13CCC(=C)[C@H](C3)C2(C)C
Molecular Weight	204.35
Reaxy-Rn	2244722
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2244722&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Molecular Weight	204.350 g/mol
XLogP3	4.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	204.188 Da
Monoisotopic Mass	204.188 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	15
Formal Charge	0
Complexity	312.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Ruiqin Zhu, Hang Mei, Huajing Liu, Changbao Hong, Xiantao Shen, Chuixiu Huang. (2022) Successive liquid-phase microextraction of acidic and basic analytes. ANALYTICA CHIMICA ACTA, 1192 (339335).
2. Zheng Chengyu, Zhou Qinan, Wang Zhenhe, Wang Jun. (2021) Behavioral responses of Platycladus orientalis plant volatiles to Phloeosinus aubei by GC-MS and HS-GC-IMS for discrimination of different invasive severity. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 413 (23): (5789-5798).
3. Chunyuan Hou, Nan Han, Bin Zhu, Xinming Li, Junmin Xi, Jianguo Fang, Yu Zhang, Jun Luo. (2025) Editing Benzotrithiophene-Based Covalent Organic Frameworks for Developing New Sonosensitizers. ACS Applied Materials & Interfaces, 17 (10): (15109-15120).
4. Mantang Chen, Linping Shi, Fuwei Xie, Xiaoyu Wang, Cong Nie, Sheng Wang, Kejian Liu, Jingjing Yu, Libin Wan. (2025) Flat membrane–based liquid-phase microextraction for the determination of basic and acidic pesticide residues in water samples. JOURNAL OF CHROMATOGRAPHY A, (465659).
5. Jingyun Cheng, Wenqi Pan, Yi Zheng, Jingyi Zhang, Liang Chen, Hui Huang, Yu Chen, Rong Wu. (2024) Piezocatalytic Schottky Junction Treats Atherosclerosis by a Biomimetic Trojan Horse Strategy. ADVANCED MATERIALS, (2312102).

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