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

auraptenol
8-(2-hydroxy-3-methyl-3-butenyl)-7-methoxycoumarin

Supplier Sponsors

Name:8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
CAS Number: 1221-43-8Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J14.363D
Molecular Weight:260.28932000
Formula:C15 H16 O4
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 "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
Boiling Point: 446.73 °C. @ 760.00 mm Hg (est)
Flash Point: 334.00 °F. TCC ( 168.00 °C. ) (est)
logP (o/w): 2.235 (est)
Soluble in:
 water, 504.3 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
(+)-Auraptenol 98%
BOC Sciences
For experimental / research use only.
Auraptenol >98%
Odor: characteristic
Use: Auraptenol is a natural coumarin found in the fruits of Citrus aurantium, it has antifibrotic activity and the anti-hyperalgesic action which may be as a novel analgesic for the management of neuropathic pain. antifibrotic, anti-hyperalgesic
Coompo
For experimental / research use only.
Auraptenol from Plants ≥96%
 
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 auraptenol usage levels up to:
 not for fragrance use.
 
Recommendation for auraptenol 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 :13343540
National Institute of Allergy and Infectious Diseases:Data
8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
 
References:
 8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):13343540
Pubchem (sid):254764744
 
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
HMDB (The Human Metabolome Database):HMDB30854
FooDB:FDB002814
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 citrus aurantium ssp. amara oil
Search Trop Picture
 orange pericarp
Search Trop Picture
 
Synonyms:
8-(2-hydroxy-3-methyl-3-butenyl)-7-methoxycoumarin
8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
 

Articles:

PubMed:Auraptenol attenuates vincristine-induced mechanical hyperalgesia through serotonin 5-HT1A receptors.
PubMed:Antidepressant-like effects of auraptenol in mice.
PubMed:Coumarins from the Herb Cnidium monnieri and chemically modified derivatives as antifoulants against Balanus albicostatus and Bugula neritina larvae.
PubMed:[Coumarins from Leonurus japonicus and their anti-platelet aggregative activity].
PubMed:Antifibrotic activity of coumarins from Cnidium monnieri fruits in HSC-T6 hepatic stellate cells.
PubMed:Nonvolatiles of commercial lime and grapefruit oils separated by high-speed countercurrent chromatography.
 
Notes:
Constit. of Seville bitter orange (Citrus aurantium ssp. amara) oil
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