Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Flavors and fragrances >  Synthetic fragrances >  Alcohols spices >  Terpenols >  Cedrol

Cedrol

Basic information Safety Supplier Related

Cedrol Basic information

Product Name:
Cedrol
Synonyms:
  • (1S,2R,5S,7R,8R)-2,6,6,8-TETRAMETHYLTRICYCLO[5.3.1.01.5]UNDECAN-8-OL
  • (1S,2R,5S,7R,8R)-2,6,6,8-Tetramethyltricyclo[5.3.1.0]undecan-8-ol
  • CYPRESS CAMPHOR
  • (+)-CEDROL
  • CEDROL
  • CEDAR CAMPHOR
  • CEDRENOL B
  • (+)-Cedrol, 98%, from Cedrus deodara (Roxb. ex Lamb.) G. Don
CAS:
77-53-2
MF:
C15H26O
MW:
222.37
EINECS:
201-035-6
Product Categories:
  • Industrial/Fine Chemicals
Mol File:
77-53-2.mol
More
Less

Cedrol Chemical Properties

Melting point:
55-59 °C(lit.)
Boiling point:
273 °C(lit.)
alpha 
D28 +9.9° (c = 5 in chloroform)
Density 
0.9479
FEMA 
4503 | (+)-CEDROL
refractive index 
n20/D1.509-1.515
Flash point:
200 °F
storage temp. 
2-8°C
solubility 
Soluble in DMSO (10 mg/ml)
form 
Solid
pka
15.35±0.60(Predicted)
color 
White
Odor
at 100.00 %. cedarwood woody dry sweet soft
Odor Type
woody
optical activity
[α]20/D +10.5±1°, c = 5% in chloroform
JECFA Number
2030
Merck 
14,1911
BRN 
2206347
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
LogP
4.33
CAS DataBase Reference
77-53-2(CAS DataBase Reference)
NIST Chemistry Reference
Cedrol(77-53-2)
EPA Substance Registry System
1H-3a,7-Methanoazulen-6-ol, octahydro-3,6,8,8-tetramethyl-, (3R,3aS,6R,7R,8aS)- (77-53-2)
More
Less

Safety Information

Safety Statements 
22-24/25
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
2
RTECS 
PB7728666
HS Code 
29062990
Hazardous Substances Data
77-53-2(Hazardous Substances Data)
Toxicity
LD50 skin in rabbit: > 5gm/kg

MSDS

More
Less

Cedrol Usage And Synthesis

Description

Cedrol is a sesquiterpene alcohol found in conifers mainly of the genera Cupressus, Juniperus, and Cedrus. It has been found to possess significant anticancer activity against glioblastoma in vitro and in vivo via cell growth inhibition, ROS generation, and DNA damage.1 Cedrol also displayed synergistic effects with temozolomide against glioblastoma in vitro and in vivo via reduced expression of drug resistance proteins.1,2 Cedrol inhibited the growth of human renal adenocarcinoma and amelanotic melanoma cells3 and induced autophagy and apoptosis in A549 non-small cell lung carcinoma cells4.

Chemical Properties

Colorless crystals; cedarwood odor. soluble in 11 parts of 95% alcohol. Combustible.

Occurrence

Found in the wood of several conifers, particularly cypresses and cedars, including Cedrus atlantica, Cupressus sempervirens, Juniperus virginiana (Fenarolfs Handbook of Flavor Ingredients, 1971).

Uses

acaricide, enhances skin ECM production

Uses

(+)-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.

Uses

In fragrances.

Definition

A tertiary terpene alcohol.

Preparation

From cedarwood by fractional distillation followed by recrystallization from suitable solvents of appropriate solid fractions.

General 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.

Purification Methods

Purify cedrol by recrystallisation from aqueous MeOH. It is estimated colorimetrically with H3PO4 in EtOH followed by vanillin and HCl [Hayward & Seymour Anal Chem 20 572 1948]. The 3,5-dinitrobenzoyl derivative has m 92-93o. [Stork & Clarke J Am Chem Soc 83 3114 1961, Beilstein 6 III 424.]

References

Chang et al. (2020), Cedrol suppresses glioblastoma progression by triggering DNA damage and blocking nuclear translocation of the androgen receptor; Cancer Lett., 495 180 Chang et al. (2020), Cedrol, a Sesquiterpene Alcohol, Enhances the Anticancer Efficacy of Temozolomide in Attenuating Drug Resistance via Regulation of the DNA Damage Response and MGMT Expression; J. Prod., 83 3021 Loizzo et al. (2008), Antiproliferative effects of essential oils and their major constituents in human renal adenocarcinoma and amelanotic melanoma cells; Cell Prolif., 41 1002 Zhang et al. (2016), Cedrol induces autophagy and apoptotic cell death in A549 non-small cell lung carcinoma cells through the PI3K/Akt signaling pathway, the loss of mitochondrial transmembrane potential and the generation of ROS; Int. J. Mol. Med., 38 291

Cedrol Preparation Products And Raw materials

Raw materials

Preparation Products

CedrolSupplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Email
sales@jingyan-chemical.com