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

suberosin
2H-1-benzopyran-2-one, 7-methoxy-6-(3-methyl-2-butenyl)- (9CI)

Supplier Sponsors

Name:7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
CAS Number: 581-31-7Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J11.513D
XlogP3-AA:3.80 (est)
Molecular Weight:244.29012000
Formula:C15 H16 O3
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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 393.30 °C. @ 760.00 mm Hg (est)
Flash Point: 331.00 °F. TCC ( 166.00 °C. ) (est)
logP (o/w): 3.870 (est)
Soluble in:
 water, 10.84 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.
Suberosin 0.99
Odor: characteristic
Use: Suberosin isolated from the roots of Angelica pubescens. It inhibits PHA-induced PBMC proliferation. anti-inflammatory;
Coompo
For experimental / research use only.
Suberosin 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 suberosin usage levels up to:
 not for fragrance use.
 
Recommendation for suberosin 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 :68486
National Institute of Allergy and Infectious Diseases:Data
7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
Chemidplus:0000581317
 
References:
 7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):68486
Pubchem (sid):135026469
 
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
FooDB:FDB005065
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
 lemon root
Search Trop Picture
 mandarin root
Search Trop Picture
 orange root
Search Trop Picture
 
Synonyms:
2H-1-benzopyran-2-one, 7-methoxy-6-(3-methyl-2-buten-1-yl)-
2H-1-benzopyran-2-one, 7-methoxy-6-(3-methyl-2-butenyl)-
2H-1-benzopyran-2-one, 7-methoxy-6-(3-methyl-2-butenyl)- (9CI)
 coumarin, 7-methoxy-6-(3-methyl-2-butenyl)-
 coumarin, 7-methoxy-6-(3-methyl-2-butenyl)- (8CI)
7-methoxy-6-(3-methyl-2-buten-1-yl)-2H-chromen-2-one
7-methoxy-6-(3-methyl-2-butenyl) coumarin
7-methoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one
7-methoxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one
7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
 

Articles:

PubMed:Anticoagulant activity of isolated coumarins (suberosin and suberenol) and toxicity evaluation of Ferulago carduchorum in rats.
PubMed:Essential oil composition of Cachrys cristata--a rare and endangered species in the flora of Serbia.
PubMed:Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
PubMed:Polyphenolic fraction of Algerian propolis protects rat kidney against acute oxidative stress induced by doxorubicin.
PubMed:[GC-MS analysis of essential oil from root of Angelica dahurica cv. Qibaizhi].
PubMed:Antibacterial mono- and sesquiterpene esters of benzoic acids from Iranian propolis.
PubMed:Isolation of xanthyletin, an inhibitor of ants' symbiotic fungus, by high-speed counter-current chromatography.
PubMed:Constituents, biological activities and quality control parameters of the crude extract and essential oil from Arracacia tolucensis var. multifida.
PubMed:Modulation of P-glycoprotein activity by acridones and coumarins from Citrus sinensis.
PubMed:Suberosin inhibits proliferation of human peripheral blood mononuclear cells through the modulation of the transcription factors NF-AT and NF-kappaB.
PubMed:Bioactive kaurane diterpenes and coumarins from Fortunella margarita.
PubMed:Cytotoxic naphthoquinones and plumbagic acid glucosides from Plumbago zeylanica.
PubMed:Antiproliferative effect of isopentenylated coumarins on several cancer cell lines.
PubMed:Antiplatelet actions of some coumarin compounds isolated from plant sources.
PubMed:Elicitor-induced biosynthesis of psoralens in Ammi majus L. suspension cultures. Microsomal conversion of demethylsuberosin into (+)marmesin and psoralen.
 
Notes:
None found
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