Sclareol

Modify Date: 2026-07-01 18:37:33

Sclareol Structure
Sclareol structure
Common Name Sclareol
CAS Number 515-03-7 Molecular Weight 308.499
Density 1.0±0.1 g/cm3 Boiling Point 398.3±15.0 °C at 760 mmHg
Molecular Formula C20H36O2 Melting Point 95-100 °C(lit.)
MSDS Chinese USA Flash Point 169.1±15.0 °C

 Use of Sclareol


Sclareol is isolated from Salvia sclarea with anticarcinogenic activity. Sclareol shows strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB) cells and human leukemia cell lines. Sclareol induces cell apoptosis[1].

Summary: Sclareol, Chinese name: 香紫苏醇, CAS number: 515-03-7, molecular formula: C20H36O2, molecular weight: 308.499. White fine powder, melting point: 95-100 °C, boiling point: 398.3±15.0 °C, density: 1.0±0.1 g/cm3. Mainly used in perfumes, fragrances, cigarettes, cosmetics, health food, food additives, etc. For research-use only, not for medical or clinical usage.


 Names

This table lists Chinese names, IUPAC names and various aliases of this chemical substance.

Name sclareol
Synonym More Synonyms

 Sclareol Biological Activity

This table contains bioactivity, target information and biological‑assay experimental data of this compound.

Description Sclareol is isolated from Salvia sclarea with anticarcinogenic activity. Sclareol shows strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB) cells and human leukemia cell lines. Sclareol induces cell apoptosis[1].
Related Catalog
In Vitro Sclareol is cytotoxic to 13 of 14 human leukemia cell lines tested, with IC50 values ranging from 6.0–24.2 μg/mL, but is not cytotoxic to peripheral blood mononuclear leukocytes within the same dose range[1].
References

[1]. Robert Tisserand, et al. Sclareol.Constituent profiles

 Chemical & Physical Properties

This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.

Density 1.0±0.1 g/cm3
Boiling Point 398.3±15.0 °C at 760 mmHg
Melting Point 95-100 °C(lit.)
Molecular Formula C20H36O2
Molecular Weight 308.499
Flash Point 169.1±15.0 °C
Exact Mass 308.271515
PSA 40.46000
LogP 5.54
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.490
InChIKey XVULBTBTFGYVRC-HHUCQEJWSA-N
SMILES C=CC(C)(O)CCC1C(C)(O)CCC2C(C)(C)CCCC21C
Storage condition 2-8C

 MSDS

This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.

 Toxicological Information

This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QK0301900
CHEMICAL NAME :
1-Naphthalenepropanol, decahydro-alpha-ethenyl-2-hydroxy-alpha,2,5,5,8a-pent amethyl-, (1R-(1-alpha(R*),2-beta,4a-beta,8a-alpha))-
CAS REGISTRY NUMBER :
515-03-7
BEILSTEIN REFERENCE NO. :
2054148
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C20-H36-O2
MOLECULAR WEIGHT :
308.56

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
FCTOD7 Food and Chemical Toxicology. (Pergamon Press Inc., Maxwell House, Fairview Park, Elmsford, NY 10523) V.20- 1982- Volume(issue)/page/year: 30,115S,1992
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
FCTOD7 Food and Chemical Toxicology. (Pergamon Press Inc., Maxwell House, Fairview Park, Elmsford, NY 10523) V.20- 1982- Volume(issue)/page/year: 30,115S,1992

 Safety Information

This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 2
RTECS QK0301900
HS Code 2906199090

 Synthetic Route

This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.

~0%

Sclareol Structure

Sclareol

CAS#:515-03-7

Learn More
Literature: Rogachev, Victor; Loehl, Thorsten; Markert, Thomas; Metz, Peter Arkivoc, 2012 , vol. 2012, # 3 p. 172 - 180

~%

Sclareol Structure

Sclareol

CAS#:515-03-7

Learn More
Literature: Leite, Mary Ann F.; Sarragiotto, Maria Helena; Imamura, Paulo M.; Marsaioli, Anita J. Journal of Organic Chemistry, 1986 , vol. 51, # 26 p. 5409 - 5410

~%

Sclareol Structure

Sclareol

CAS#:515-03-7

Learn More
Literature: Scheidegger,U. et al. Helvetica Chimica Acta, 1962 , vol. 45, p. 400 - 435

 Customs

This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.

HS Code 2906199090
Summary 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles27

More Articles

This table lists relevant public references with title, journal and publication metadata for this compound.

Parallel dual secondary column-dual detection: a further way of enhancing the informative potential of two-dimensional comprehensive gas chromatography.

J. Chromatogr. A. 1360 , 264-74, (2014)

Comprehensive two-dimensional gas chromatography (GC×GC) coupled with Mass Spectrometry (MS) is one of today's most powerful analytical platforms for detailed analysis of medium-to-high complexity sam...

Labdane diterpenoids from Salvia reuterana.

Phytochemistry 108 , 264-9, (2014)

Three labdane diterpenoids, 14α-hydroxy-15-chlorosclareol (1), 14α-hydroxy-15-acetoxysclareol (2), and 6β-hydroxy-14α-epoxysclareol (3), together with the known diterpenoids sclareol (4), 6β-hydroxysc...

Isolation, chemical, and biotransformation routes of labdane-type diterpenes.

Chem. Rev. 111(8) , 4418-52, (2011)

 SclareolBioassay

View more

This table contains target information, in‑vitro & in‑vivo assay data for this compound.

Name: Minimum inhibitory concentration against Escherichia coli (ATCC 25922)
Source: ChEMBL
Target: Escherichia coli
External Id: CHEMBL677995
Name: p53 small molecule agonists, cell-based qHTS assay
Source: 824
External Id: P53344
Name: p53 small molecule agonists, cell-based qHTS assay with human liver microsomes
Source: 824
Target: tumor suppressor p53 [Homo sapiens]
External Id: P53MS233
Name: p53 small molecule agonists, cell-based qHTS assay with rat liver microsomes
Source: 824
Target: tumor suppressor p53 [Homo sapiens]
External Id: P53MS898
Total 232, Current Page 1 of 24
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 Synonyms

This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.

(1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-methyl-4-penten-1-yl]-2,5,5,8a-tetramethyldecahydro-2-naphthalenol
(1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-methylpent-4-en-1-yl]-2,5,5,8a-tetramethyldecahydronaphthalen-2-ol
SCLAREOL(RG)
EINECS 208-194-0
SCIADONIC ACID
(1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol
labd-14-ene-8,13(R)-diol
MFCD00869558
SCLAREOL,NATURAL
SCAREOL
Sclareol
(-)-sclareol
SCLAREOL(P)
(1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-méthyl-4-pentèn-1-yl]-2,5,5,8a-tétraméthyldécahydro-2-naphtalénol

 Sclareol | FAQ

This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.

Q: What is the melting point of sclareol?
A: Melting point of sclareol is 95-100 °C(lit.).
Q: What is the molecular formula of sclareol?
A: Molecular formula of sclareol is C20H36O2.
Q: What is the English name of sclareol?
A: The English name of sclareol is sclareol.
Q: What are the upstream materials of sclareol?
A: Related upstream materials(CAS) of sclareol: 54274-72-5;1158-77-6;596-85-0.
Q: What is the boiling point of sclareol?
A: Boiling point of sclareol is 398.3±15.0 °C at 760 mmHg.
Q: What are the uses of sclareol?
A: Main uses of sclareol: Sclareol is isolated from Salvia sclarea with anticarcinogenic activity. Sclareol shows strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB) cells and human leukemia cell lines. Sclareol induces cell apoptosis[1].
Q: What is the LogP of sclareol?
A: LogP of sclareol is 5.54.
Q: What is the SMILES notation of sclareol?
A: SMILES notation of sclareol is C=CC(C)(O)CCC1C(C)(O)CCC2C(C)(C)CCCC21C.
Q: What are the storage conditions for sclareol?
A: Storage conditions for sclareol: 2-8C.
Q: What is the CAS number of sclareol?
A: CAS number of sclareol is 515-03-7.

 Sclareolfactory

This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.

Shanghai Nianxing Industrial Co., Ltd
BioBioPha
naturewill
Henan Tianfu Chemical Co., Ltd.
Zhongshan Xingrui Chemical Co. , Ltd.
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