EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

hydroxyanigorufone

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CAS Number: 56252-02-9Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J842.711I
XlogP3-AA:4.30 (est)
Molecular Weight:288.30224000
Formula:C19 H12 O3
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
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Google Scholar: with word "odor"Search
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
Soluble in:
 water, 2.482 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.
Hydroxyanigorufone 96%
Odor: characteristic
Use: Hydroxyanigorufone is a natural compound isolated from the fruits of Musa itin
 
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 hydroxyanigorufone usage levels up to:
 not for fragrance use.
 
Recommendation for hydroxyanigorufone 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 :11471752
National Institute of Allergy and Infectious Diseases:Data
2-hydroxy-9-(4-hydroxyphenyl)phenalen-1-one
 
References:
 2-hydroxy-9-(4-hydroxyphenyl)phenalen-1-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):11471752
Pubchem (cas):56252-02-9
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB34449
FooDB:FDB012856
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
 musa acuminata pigment
Search Trop Picture
 
Synonyms:
2-hydroxy-9-(4-hydroxyphenyl)phenalen-1-one
 

Articles:

PubMed:Concise Synthesis of Natural Phenylphenalenone Phytoalexins and a Regioisomer.
PubMed:Diarylheptanoids and phenylphenalenones from Musa itinerans fruits.
PubMed:Radical scavenging capacity of 2,4-dihydroxy-9-phenyl-1H-phenalen-1-one: a functional group exclusion approach.
PubMed:Phyllosticta musarum Infection-Induced Defences Suppress Anthracnose Disease Caused by Colletotrichum musae in Banana Fruits cv 'Embul'.
PubMed:[Active compounds from rhizomes of Musa basjoo].
PubMed:The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis.
PubMed:Constituents of Musa x paradisiaca cultivar with the potential to induce the phase II enzyme, quinone reductase.
PubMed:Dimeric phenylphenalenones from Musa acuminata and various Haemodoraceae species. Crystal structure of anigorootin.
PubMed:Changes in the content and biosynthesis of phytoalexins in banana fruit.
 
Notes:
None found
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