osthenol
2H-1-benzopyran-2-one, 7-hydroxy-8-(3-methyl-2-butenyl)-
 
Notes:
Isol. from seeds of Apium graveolens
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      484-14-0 Osthenol
       
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CAS Number: 484-14-0Picture of molecule3D/inchi
FDA UNII: 7X6RF2708X
Nikkaji Web: J12.528H
XlogP3-AA: 3.50 (est)
Molecular Weight: 230.26318000
Formula: C14 H14 O3
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome 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: 422.00 to  423.00 °C. @ 760.00 mm Hg (est)
Flash Point: 363.00 °F. TCC ( 184.10 °C. ) (est)
logP (o/w): 3.342 (est)
Soluble in:
 water, 148.1 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.
Osthenol
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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 osthenol usage levels up to:
 not for fragrance use.
 
Recommendation for osthenol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5320318
National Institute of Allergy and Infectious Diseases: Data
 7-hydroxy-8-(3-methylbut-2-enyl)chromen-2-one
Chemidplus: 0000484140
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References:
 7-hydroxy-8-(3-methylbut-2-enyl)chromen-2-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5320318
Pubchem (sid): 135116445
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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
KEGG (GenomeNet): C18080
HMDB (The Human Metabolome Database): HMDB34130
FooDB: FDB012404
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: 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
 ashitaba
Search Trop  Picture
 celery seed
Search Trop  Picture
 fennel seed
Search Trop  Picture
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Synonyms:
2H-1-benzopyran-2-one, 7-hydroxy-8-(3-methyl-2-buten-1-yl)-
2H-1-benzopyran-2-one, 7-hydroxy-8-(3-methyl-2-butenyl)-
7-hydroxy-8-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one
7-hydroxy-8-(3-methyl-but-2-enyl)-chromen-2-one
7-hydroxy-8-(3-methylbut-2-en-1-yl)-2H-chromen-2-one
7-hydroxy-8-(3-methylbut-2-enyl)chromen-2-one
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Articles:
PubMed: A coumarin-specific prenyltransferase catalyzes the crucial biosynthetic reaction for furanocoumarin formation in parsley.
PubMed: Isolation and identification of metabolites of osthole in rats.
PubMed: An efficient strategy based on MAE, HPLC-DAD-ESI-MS/MS and 2D-prep-HPLC-DAD for the rapid extraction, separation, identification and purification of five active coumarin components from Radix Angelicae Dahuricae.
PubMed: Antifungal activity of coumarins.
PubMed: High-performance liquid chromatographic method for the determination and pharmacokinetic study of oxypeucedanin hydrate and byak-angelicin after oral administration of Angelica dahurica extracts in mongrel dog plasma.
PubMed: Antibacterial activity of coumarins.
PubMed: Separation and quantitative analysis of coumarin compounds from Angelica dahurica (Fisch. ex Hoffm) Benth. et Hook. f by pressurized capillary electrochromatography.
PubMed: Antitumor-promoting activity of coumarins from citrus plants.
PubMed: Inhibitors of 5alpha -reductase type I in LNCaP cells from the roots of Angelica koreana.
PubMed: Inhibition of concanavalin A-induced mice hepatitis by coumarin derivatives.
PubMed: Inhibitory effects of Angelica pubescens f. biserrata on 5-lipoxygenase and cyclooxygenase.
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