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pinobanksin-3-acetate
4H-1-benzopyran-4-one, 3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R,3R)-

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CAS Number: 52117-69-8Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J894.646I
XlogP3-AA:2.80 (est)
Molecular Weight:314.29378000
Formula:C17 H14 O6
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
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Google Scholar: with word "flavor"Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 547.60 °C. @ 760.00 mm Hg (est)
Flash Point: 401.00 °F. TCC ( 205.10 °C. ) (est)
logP (o/w): 3.850 (est)
Soluble in:
 water, 250.6 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
3-O-Acetylpinobanksin
Coompo
For experimental / research use only.
3-O-Acetylpinobanksin from Plants
Santa Cruz Biotechnology
For experimental / research use only.
Pinobanksin acetate
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for pinobanksin-3-acetate usage levels up to:
 not for fragrance use.
 
Recommendation for pinobanksin-3-acetate flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :148556
National Institute of Allergy and Infectious Diseases:Data
[(2R,3R)-5,7-dihydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate
Chemidplus:0052117698
 
References:
 [(2R,3R)-5,7-dihydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):148556
Pubchem (sid):135105922
 
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
KEGG (GenomeNet):C16418
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 honey
Search PMC Picture
 
Synonyms:
(2R-trans)-3-(acetyl oxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one
(2R-trans)-3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one
3-O-acetylpinobanksin
4H-1-benzopyran-4-one, 3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R-trans)-
4H-1-benzopyran-4-one, 3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R,3R)-
[(2R,3R)-5,7-dihydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate
(2R,3R)-5,7-dihydroxy-4-oxo-2-phenyl-3,4-dihydro-2H-chromen-3-yl acetate
 

Articles:

PubMed:Chemical composition, antioxidant and anti-AGEs activities of a French poplar type propolis.
PubMed:Chemical and functional characterisation of propolis collected from East Andalusia (southern Spain).
PubMed:Identification and quantification of phytochemical composition and anti-inflammatory and radical scavenging properties of methanolic extracts of Chinese propolis.
PubMed:Propolis with high flavonoid content collected by honey bees from Acacia paradoxa.
PubMed:Two new cytotoxic phenylallylflavanones from Mexican propolis.
PubMed:Negative ion 'chip-based' nanospray tandem mass spectrometry for the analysis of flavonoids in glandular trichomes of Lychnophora ericoides Mart. (Asteraceae).
PubMed:Evaluation of propolis polyphenols absorption in humans by liquid chromatography/tandem mass spectrometry.
PubMed:Sonoran propolis: chemical composition and antiproliferative activity on cancer cell lines.
PubMed:Antioxidant compounds of propolis determined by capillary electrophoresis-mass spectrometry.
PubMed:Trypanocidal activity of Lychnophora staavioides Mart. (Vernonieae, Asteraceae).
PubMed:The effect of flavonoids on ofloxacin-induced mutagenicity in Euglena gracilis.
PubMed:Redox intermediates of flavonoids and caffeic acid esters from propolis: an EPR spectroscopy and cyclic voltammetry study.
PubMed:[On the antimicrobial activity of propolis and propolis constituents (author's transl)].
 
Notes:
None found
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