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Cedrol - >98.0%(GC), high purity , CAS No.77-53-2

  • ≥98%(GC)
Item Number
C154086
Grouped product items
SKUSizeAvailabilityPrice Qty
C154086-5g
5g
In stock
$93.90
C154086-25g
25g
In stock
$205.90
C154086-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$738.90
C154086-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$3,324.90
View related series
terpenes

Basic Description

SynonymsCedrol|(+)-Cedrol|77-53-2|alpha-Cedrol|8betaH-Cedran-8-ol|(8R)-cedran-8-ol|8.beta.H-Cedran-8-ol|CHEMBL1974890|DTXSID1041269|CHEBI:10217|63ZM9703BO|NSC403883|NSC-403883|[3R-(3alpha,3abeta,6alpha,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methano
Specifications & Purity≥98%(GC)
Shipped InNormal
Product Description

Product Description
(+)-Cedrol is a crystalline hydrated product of α-cedrene, which is a sesquiterpene found in cedar-wood oil. It can be used as a fragrance ingredient in cosmetics, shampoos, and soaps as well as in non-cosmetic products such as cleaners and detergents. (±) Cedrol can be synthesized by intramolecular Diels-Alder reaction of alkyl cyclopentadiene.
Product Application
(+)-Cedrol can be used as a starting material for the preparation of cedryl acetate by acetylation using acetic anhydride in the presence of an acid catalyst. It can also be incorporated as a precursor for the total synthesis of rare illicium sesquiterpene (+)-pseudoanisatin via selective C-H bond functionalization.

Associated Targets

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK12 Tchem Mitogen-activated protein kinase 12 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AKT3 Tchem RAC-gamma serine/threonine-protein kinase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488183692
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183692
IUPAC Name (1S,2R,5S,7R,8R)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecan-8-ol
INCHI InChI=1S/C15H26O/c1-10-5-6-11-13(2,3)12-9-15(10,11)8-7-14(12,4)16/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14-,15+/m1/s1
InChi Key SVURIXNDRWRAFU-OGMFBOKVSA-N
Canonical SMILES CC1CCC2C13CCC(C(C3)C2(C)C)(C)O
Isomeric SMILES C[C@@H]1CC[C@@H]2[C@]13CC[C@@]([C@H](C3)C2(C)C)(C)O
WGK Germany 2
RTECS PB7728666
PubChem CID 65575
Molecular Weight 222.37
Beilstein 2206350

Certificates

Certificate of Analysis(COA)

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7 results found

Lot NumberCertificate TypeDateItem
A2306144Certificate of AnalysisJun 29, 2022 C154086
D2407033Certificate of AnalysisJun 29, 2022 C154086
F2310688Certificate of AnalysisJun 29, 2022 C154086
I2202393Certificate of AnalysisJun 29, 2022 C154086
I2202395Certificate of AnalysisJun 29, 2022 C154086
I2202400Certificate of AnalysisJun 29, 2022 C154086
I2202475Certificate of AnalysisJun 29, 2022 C154086

Chemical and Physical Properties

SolubilityInsoluble in water; Soluble in Chloroform
Specific Rotation[α]+10.5±1°, c = 5% in chloroform
Boil Point(°C)273°C
Melt Point(°C)82-86°C

Safety and Hazards(GHS)

WGK Germany 2
RTECS PB7728666
Merck Index 1911

Related Documents

Solution Calculators