evernic acid

4-((4-methoxy-6-methylsalicyloyl)oxy)-6-methylsalicylic acid

CAS: 537-09-7 C17 H16 O7 MW: 332.30892000

Identification

Nameevernic acid
IUPAC2-hydroxy-4-(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy-6-methylbenzoic acid
CAS Number537-09-7
EINECS208-658-2
FDA UNII2EQ5W5403J
Molecular FormulaC17 H16 O7
Molecular Weight332.30892000
MDL NumberMFCD00045824
Nikkaji NumberJ13.675A
Beilstein2227186

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 531.80 °C. @ 760.00 mm Hg (est)
Flash Point 382.00 °F. TCC ( 194.60 °C. ) (est)
logP (o/w) 5.030 (est)
Soluble in water, 4.404 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral Toxicityintravenous-mouse LD50 178 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01633']

Safety in Use

Categorynatural substances and extractives
Recommendation for evernic acid usage levels up tonot for fragrance use.
Recommendation for evernic acid flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

oakmoss

Synonyms

4-((4- methoxy-6-methyl salicyloyl)oxy)-6-methyl salicylic acid 2,6- cresotic acid, 4-methoxy-, 4-ester with 6-methyl-beta-resorcylic acid (8CI) 4-((4- methoxy-6-methylsalicyloyl)oxy)-6-methylsalicylic acid 2- hydroxy-4-(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy-6-methylbenzoic acid 2- hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methylbenzoic acid PubMed: Clastogenic effect of atranorin, evernic acid, and usnic acid on human lymphocytes. PubMed: [Study on the chemical constituents of two lichen plants from Meng Mountain]. PubMed: Potential of lichen secondary metabolites against Plasmodium liver stage parasites with FAS-II as the potential target. PubMed: Antiproliferative effects on tumour cells and promotion of keratinocyte wound healing by different lichen compounds. PubMed: Fragrance chemicals in domestic and occupational products. PubMed: Improvement of the analysis of dansylated derivatives of polyamines and their conjugates by high-performance liquid chromatography. PubMed: Separation of polyamines, conjugated to DNA, by reversed-phase high-performance liquid chromatography. PubMed: Screening of tissue cultures and thalli of lichens and some of their active constituents for inhibition of tumor promoter-induced Epstein-Barr virus activation. PubMed: An investigation of the allergenic constituents of Cladonia stellaris (Opiz) Pous & Vezda ('silver moss', 'reindeer moss' or 'reindeer lichen'). PubMed: The occurrence of lichen phenolics in the photobiont cells of Evernia prunastri. PubMed: Photosensitivity to oak moss. PubMed: The use of immobilized cells to stabilize orsellinate depside hydrolase of Pseudevernia furfuracea. PubMed: Purification and Properties of the Constitutive Arginase of Evernia prunastri. PubMed: The use of urea by Evernia prunastri thalli. PubMed: A Simple Assay Demonstrating the Effect of Rehydration on the Orsellinate Depside Hydrolase Activity of Evernia prunastri. PubMed: Endogenous Inactivators of Arginase, l-Arginine Decarboxylase, and Agmatine Amidinohydrolase in Evernia prunastri Thallus. PubMed: Contact allergy to atranorin in lichens and perfumes.