(+)-Usniacin Chemical Properties

Melting point:

201-203 °C(lit.)

alpha 

488 º (c=0.4, CHCl3)

Boiling point:

399.43°C (rough estimate)

Density 

1.2869 (rough estimate)

refractive index 

1.4790 (estimate)

storage temp. 

Sealed in dry,Room Temperature

solubility 

almost transparency in Chloroform

form 

powder to crystal

pka

4.00±0.40(Predicted)

color 

Light orange to Yellow to Green

optical activity

[α]25/D +488°, c = 0.7% in chloroform

Water Solubility 

Partly soluble in water. Soluble in acetone, ethanol, chloroform and furfural.

Merck 

14,9893

BRN 

96698

LogP

1.270 (est)

CAS DataBase Reference

7562-61-0(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

Safety Statements 

36

WGK Germany 

3

RTECS 

HP5295050

F 

3-10

HazardClass 

IRRITANT

HS Code 

29329990

MSDS

• Language:English Provider:SigmaAldrich

(+)-Usniacin Usage And Synthesis

Preparation

Weigh 5.0 g of chopped Usnea longiflora into a 500 mL flask, and extract with 75 mL of ethyl acetate for 2 times, 4 h each time, and combine the extracts. Suction filtration, concentrated to 1/6~1/8 of the original volume, naturally cooled, crystallized, filtered off the mother liquor, and dried at 80°C to obtain the crude usnic acid. 30 times the amount of benzene-ethanol (volume ratio 1:1) mixed solvent was added to the crude product, refluxed for 2 h, filtered while hot, the filtrate was concentrated to 1/5 of the original volume, and crystals were precipitated by cooling. Dry at 80 ℃, recrystallize twice with ethyl acetate, and the obtained relatively pure pale yellow needle crystal is the fine usnic acid.

Uses

Usnic acid is used as fragrance; preservative in deodorants; in anti ac ne formulations; antibiotic for topical application.

Uses

Usnic Acid acts as an antibacterial and antifungal agent, and are often seen used in cosmetics and facial application chemicals.

Uses

(+)-Usnic acid has been used to study the following:

• The mechanism of its antimicrobial activity in bacterial cells.
• Its ability as an antibiofilm agent against Group A Streptococci (GAS).
• Its ability as a potent anti-virulent compound against Candida albicans.
• The mechanism of its toxic effect on hepatocytes.
• Its ability to inhibit the motility of human lung cancer cells.

Definition

ChEBI: (-)-usnic acid is the (-)-enantiomer of usnic acid. It has a role as an EC 1.13.11.27 (4-hydroxyphenylpyruvate dioxygenase) inhibitor. It is a conjugate acid of a (-)-usnic acid(2-). It is an enantiomer of a (+)-usnic acid.

General Description

(+)-Usniacin is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG.

Biological Activity

mic: 0.05 μg/62.5 μl to 3.1 μg/62.5 μlmicroorganisms can colonize a wide variety of medical devices, putting patients at risk for systemic and local infectious complications, including local-site infections, endocarditis, and catheter-related bloodstream infections. (+)-usniacin is a secondary lichen metabolite that possesses antimicrobial activity against various planktonic gram-positive bacteria.

Contact allergens

Usnic acid is a component of lichens, also used as a topical antibiotic. Allergic contact dermatitis from lichens occurs mainly occupationally in forestry and horticultural workers, and in lichen pickers.

in vitro

(+)-usniacin showed antimicrobial activity against the same microorganisms as that of acetone extract. among the three analogues it was the most active one having quite low mic values. furthermore, (+)-usniacin did not show any activity against a. hydrophila and b. cereus whereas (d)-usnic acid did. on the other hand, (+)-usniacin was active against y. enterocolitica whereas (d)-usnic acid was not active [1].

Purification Methods

This very weak acid is the natural form which is recrystallised from Me2CO, MeOH or *C6H6. At 25o it is soluble in H2O (<0.01%), Me2CO (0.77%), EtOAc (0.88%), MeOCH2CH2OH (0.22%) and furfural (7.32%). [Curd & Robertson J Chem Soc 894 1937, Barton & Brunn J Chem Soc 603 1953, resolution: Dean et al. J Chem Soc 1250 1953, synthesis: Barton et al. J Chem Soc 538 1956, Beilstein 18/5 V 586.]

References

[1] tay t, türk ao, yilmaz m, türk h, kivanç m. evaluation of the antimicrobial activity of the acetone extract of the lichen ramalina farinacea and its (+)-usnic acid, norstictic acid, and protocetraric acid constituents. z naturforsch c. 2004 may-jun;59(5-6):384-8.
[2] ghione m, parrello d, grasso l. usnic acid revisited, its activity on oral flora. chemioterapia. 1988 oct;7(5):302-5.

(+)-Usniacin(7562-61-0)Related Product Information

• Dimethyl phthalate
• Dimethyl sebacate
• Dimethyl sulfoxide
• Ethyl 2-(Chlorosulfonyl)acetate
• N,N-Dimethylformamide
• 2,3-Butanedione
• N-ACETYL-L-TYROSINE ETHYL ESTER
• Dimethyl fumarate
• 4,4'-Diacetylbiphenyl
• Dimethyl ether
• Glycine
• Citric acid
• Stearic acid
• Folic acid
• Tetraacetylethylenediamine
• ETHANE
• Dimethyl carbonate
• Ascoric Acid