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

pabulenol

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CAS Number: 33889-70-2Picture of molecule3D/inchi
FDA UNII: 1P9F66D29E
Nikkaji Web:J181.328E
XlogP3-AA:2.90 (est)
Molecular Weight:286.28358000
Formula:C16 H14 O5
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
Soluble in:
 water, 359.9 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.
pabulenol >98%
 
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 pabulenol usage levels up to:
 not for fragrance use.
 
Recommendation for pabulenol 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 :3009225
National Institute of Allergy and Infectious Diseases:Data
4-[(2S)-2-hydroxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one
Chemidplus:0033889702
 
References:
 4-[(2S)-2-hydroxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):3009225
Pubchem (cas):33889-70-2
 
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):Search
FooDB:FDB011916
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
 angelica genuflexa
Search Trop Picture
 citrus limon fruit
Search Trop Picture
 
Synonyms:
7H-furo(3,2-g)(1)benzopyran-7-one, 4-(((2S)-hydroxy-3-methyl-3-butenyl)oxy)-
4-[(2S)-2-hydroxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one
(S)-pabulenol
 

Articles:

PubMed:[Chemical constituents from lipophilic parts in roots of Angelica dahurica cv.Yubaizhi].
PubMed:A review of the ethnopharmacology, phytochemistry and pharmacology of Notopterygium incisum.
PubMed:[Chemical constituents from lipophilic parts in roots of Angelica dahurica var. formosana cv. Chuanbaizhi].
PubMed:Preliminary in vitro and in vivo evaluation of antidiabetic activity of Ducrosia anethifolia Boiss. and its linear furanocoumarins.
PubMed:[A new natural product from root of Angelica dahurica cv. Qibaizhi].
PubMed:[Studies on chemical constituents from roots of Angelica polymorpha].
PubMed:[Studies on chemical constituents in roots and rhizomes of Notopterygium incisum].
PubMed:[Chemical constituents of antibacterial activity fraction of Angelica polymorpha].
PubMed:Nonvolatiles of commercial lime and grapefruit oils separated by high-speed countercurrent chromatography.
PubMed:Antioxidative activity of furanocoumarins isolated from Angelicae dahuricae.
PubMed:Platelet anti-aggregatory effects of coumarins from the roots of Angelica genuflexa and A. gigas.
PubMed:Studies on the antitumor-promoting activity of naturally occurring substances. II. Inhibition of tumor-promoter-enhanced phospholipid metabolism by umbelliferous materials.
 
Notes:
None found
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