methyl orsellinate
benzoic acid, 2,4-dihydroxy-6-methyl-, methyl ester
 
Notes:
None found
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    • BOC Sciences
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      Product(s):
      3187-58-4 Methyl orsellinate
      Methyl orsellinate is purified from the herbs of Dianella ensifolia (L.) DC.2.
       
       
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CAS Number: 3187-58-4Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web: J113.556B
XlogP3-AA: 2.00 (est)
Molecular Weight: 182.17550000
Formula: C9 H10 O4
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 339.10 °C. @ 760.00 mm Hg (est)
Flash Point: 281.00 °F. TCC ( 138.10 °C. ) (est)
logP (o/w): 2.380 (est)
Soluble in:
 water, 1070 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Methyl orsellinate
Odor: characteristic
Use: Methyl orsellinate is purified from the herbs of Dianella ensifolia (L.) DC.2.
Coompo
For experimental / research use only.
Methyl Orsellinate from Plants ≥96%
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for methyl orsellinate usage levels up to:
 not for fragrance use.
 
Recommendation for methyl orsellinate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 3187-58-4
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 76658
National Institute of Allergy and Infectious Diseases: Data
 methyl 2,4-dihydroxy-6-methylbenzoate
Chemidplus: 0003187584
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References:
 methyl 2,4-dihydroxy-6-methylbenzoate
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 76658
Pubchem (sid): 135035021
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): Search
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 found in nature
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Synonyms:
 benzoic acid, 2,4-dihydroxy-6-methyl-, methyl ester
2,4-dihydroxy-6-methyl benzoic acid methyl ester
 methyl 2,4-dihydroxy-6-methyl benzoate
 methyl 2,4-dihydroxy-6-methylbenzoate
 methyl o-orsellinate
 methyl orselinate
 orsellinic acid monomethyl ester
b-resorcylic acid, 6-methyl-, methyl ester
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Articles:
PubMed: A new depside from Usnea aciculifera growing in Vietnam.
PubMed: Synthesis of macrolactam analogues of radicicol and their binding to heat shock protein Hsp90.
PubMed: [Determination of atranol, lecanorin, ethyl orsellinate and methyl orsellinate in Usnea diffracta by RP-HPLC].
PubMed: In vitro antitumour activity of orsellinates.
PubMed: PTP1B inhibitory effects of tridepside and related metabolites isolated from the Antarctic lichen Umbilicaria antarctica.
PubMed: [Studies on the chemical constituents of Phellodendron chinense].
PubMed: [Chemical constituents from barks of Garcinia tetralata].
PubMed: Enzymatic production of atranorin: a component of the oak moss absolute by immobilized lichen cells.
PubMed: Phytotoxic compounds from Flourensia cernua.
PubMed: Effects of tenuiorin and methyl orsellinate from the lichen Peltigera leucophlebia on 5-/15-lipoxygenases and proliferation of malignant cell lines in vitro.
PubMed: Effect of lichen metabolites on thylakoid electron transport and photophosphorylation in isolated spinach chloroplasts.
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