CAS 4630-07-3|valencene

Introduction：Basic information about CAS 4630-07-3|valencene, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. valencene BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Synonyms

Common Name	valencene
CAS Number	4630-07-3	Molecular Weight	204.35100
Density	0.89g/cm3	Boiling Point	270.5ºC at 760mmHg
Molecular Formula	C₁₅H₂₄	Melting Point	/
MSDS	ChineseUSA	Flash Point	106ºC

Names

Name	(+)-valencene
Synonym	More Synonyms

valencene BiologicalActivity

Description	Valencene is a sesquiterpene isolated from Cyperus rotundus, possesses antiallergic, antimelanogenesis, anti-infammatory, and antioxidant activitivies. Valencene inhibits the exaggerated expression of Th2 chemokines and proinflammatory chemokines through blockade of the NF-κB pathway. Valencene is used to flavor foods and drinks[1][2][3].
Related Catalog	Research Areas >>Inflammation/Immunology
References	[1]. Yang IJ, et al. Inhibitory Effect of Valencene on the Development of Atopic Dermatitis-Like Skin Lesions in NC/Nga Mice. Evid Based Complement Alternat Med. 2016;2016:9370893. [2]. Frohwitter J, et al. Production of the sesquiterpene (+)-valencene by metabolically engineered Corynebacterium glutamicum. J Biotechnol. 2014 Dec 10;191:205-13. [3]. Marques FM, et al. In vitro anti-inflammatory activity of terpenes via suppression of superoxide and nitric oxide generation and the NF-κB signalling pathway. Inflammopharmacology. 2019 Apr;27(2):281-289.

Description

Valencene is a sesquiterpene isolated from Cyperus rotundus, possesses antiallergic, antimelanogenesis, anti-infammatory, and antioxidant activitivies. Valencene inhibits the exaggerated expression of Th2 chemokines and proinflammatory chemokines through blockade of the NF-κB pathway. Valencene is used to flavor foods and drinks[1][2][3].

Related Catalog

Research Areas >>Inflammation/Immunology

References

[1]. Yang IJ, et al. Inhibitory Effect of Valencene on the Development of Atopic Dermatitis-Like Skin Lesions in NC/Nga Mice. Evid Based Complement Alternat Med. 2016;2016:9370893.

[2]. Frohwitter J, et al. Production of the sesquiterpene (+)-valencene by metabolically engineered Corynebacterium glutamicum. J Biotechnol. 2014 Dec 10;191:205-13.

[3]. Marques FM, et al. In vitro anti-inflammatory activity of terpenes via suppression of superoxide and nitric oxide generation and the NF-κB signalling pathway. Inflammopharmacology. 2019 Apr;27(2):281-289.

Chemical & Physical Properties

Density	0.89g/cm3
Boiling Point	270.5ºC at 760mmHg
Molecular Formula	C₁₅H₂₄
Molecular Weight	204.35100
Flash Point	106ºC
Exact Mass	204.18800
LogP	4.72520
Index of Refraction	n20/D 1.504(lit.)
InChIKey	QEBNYNLSCGVZOH-NFAWXSAZSA-N
SMILES	C=C(C)C1CCC2=CCCC(C)C2(C)C1
Storage condition	2-8°C

Safety Information

Personal Protective Equipment	Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
Safety Phrases	S23-S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3

Synonyms

FEMA 3443

(3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene

(1R,7R,8aS)-1,2,3,5,6,7,8,8a-octahydro-1,8a-dimethyl-7-(1-methylethenyl)naphthalene

MFCD00075884

(R)-Valencene

Valencen

EINECS 225-047-6

VALENCE

VALENCENE 85

VALENCENE

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