CAS 89-79-2|ISOPULEGOL

Introduction：Basic information about CAS 89-79-2|ISOPULEGOL, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. ISOPULEGOL BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Articles5
7. Synonyms

Common Name	ISOPULEGOL
CAS Number	89-79-2	Molecular Weight	154.24900
Density	0.912 g/mL at 25 °C(lit.)	Boiling Point	212 °C(lit.)
Molecular Formula	C₁₀H₁₈O	Melting Point	/
MSDS	ChineseUSA	Flash Point	195 °F
Symbol	GHS07	Signal Word	Warning

Names

Name	isopulegol
Synonym	More Synonyms

ISOPULEGOL BiologicalActivity

Description	(-)-Isopulegol is prepared directly from the treatment of essential oil of citronella under solid supported acid catalysis and solvent-free microwave assisted ene-cyclisation. (-)-Isopulegol shows high activity in reacting with carbonyl compounds. (-)-Isopulegol can be used for antiviral activity research[1].
Related Catalog	Research Areas >>InfectionSignaling Pathways >>Others >>Others
References	[1]. Raquel G.Jacob, et al. Green synthesis of (−)-isopulegol from (+)-citronellal: application to essential oil of citronella. Tetrahedron Letters. 2003 April 28;44(18):3605-3608. [2]. Ilyina IV, et al. Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses. Bioorg Med Chem Lett. 2018 Jun 15;28(11):2061-2067.

Description

(-)-Isopulegol is prepared directly from the treatment of essential oil of citronella under solid supported acid catalysis and solvent-free microwave assisted ene-cyclisation. (-)-Isopulegol shows high activity in reacting with carbonyl compounds. (-)-Isopulegol can be used for antiviral activity research[1].

Related Catalog

Research Areas >>InfectionSignaling Pathways >>Others >>Others

References

[1]. Raquel G.Jacob, et al. Green synthesis of (−)-isopulegol from (+)-citronellal: application to essential oil of citronella. Tetrahedron Letters. 2003 April 28;44(18):3605-3608.

[2]. Ilyina IV, et al. Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses. Bioorg Med Chem Lett. 2018 Jun 15;28(11):2061-2067.

Chemical & Physical Properties

Density	0.912 g/mL at 25 °C(lit.)
Boiling Point	212 °C(lit.)
Molecular Formula	C₁₀H₁₈O
Molecular Weight	154.24900
Flash Point	195 °F
Exact Mass	154.13600
PSA	20.23000
LogP	2.35960
Index of Refraction	n20/D 1.471(lit.)
InChIKey	ZYTMANIQRDEHIO-KXUCPTDWSA-N
SMILES	C=C(C)C1CCC(C)CC1O
Storage condition	?20°C

Safety Information

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H302-H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes	Xn: Harmful;
Risk Phrases	R21/22
Safety Phrases	S26-S36/37/39
RIDADR	NA 1993 / PGIII
WGK Germany	2
HS Code	2906199090

Customs

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%

Articles5

Modifications of the chemical structure of terpenes in antiplasmodial and antifungal drug research.

Bioorg. Med. Chem. Lett. 17 , 6075-8, (2007)

Pure natural monoterpenes were evaluated in vitro for their antiplasmodial activities against Plasmodium falciparum. Chemically modified terpenes were also tested to see whether the introduction of an...

[The metabolic products of microorganisms. Boromycin].

Helv. Chim. Acta 50 , 153, (1967)

G. Schmid, W. Hofheinz

J. Am. Chem. Soc. 105 , 624, (1983)

Synonyms

(-)-Isopulegol

ISOPULEGOL (P-MENTH-8-EN-3-OL)

ISO-PULEGOL

ISOPULEGOL

EINECS 201-940-6

MFCD00134655

FEMA 2962

P-MENTH-8-EN-3-OL

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