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beta-hydroxypropiovanillone
1-propanone, 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-

Supplier Sponsors

Name:3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
CAS Number: 2196-18-1Picture of molecule3D/inchi
FDA UNII: M22UI268J1
Nikkaji Web:J102.027G
XlogP3:-0.20 (est)
Molecular Weight:196.20244000
Formula:C10 H12 O4
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: 408.00 to 409.00 °C. @ 760.00 mm Hg (est)
Flash Point: 330.00 °F. TCC ( 165.40 °C. ) (est)
logP (o/w): 0.622 (est)
Soluble in:
 water, 1.356e+005 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.
b-Hydroxypropiovanillone 0.97
Odor: characteristic
Use: b-Hydroxypropiovanillone isolated from the barks of Pinus yunnanensis. It shows potent tyrosinase inhibitory activity.
Coompo
For experimental / research use only.
beta-Hydroxypropiovanillone 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 beta-hydroxypropiovanillone usage levels up to:
 not for fragrance use.
 
Recommendation for beta-hydroxypropiovanillone 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 :75142
National Institute of Allergy and Infectious Diseases:Data
3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
Chemidplus:0002196181
 
References:
 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):75142
Pubchem (sid):135032593
 
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):Search
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
 ligusticum porteri
Search Trop Picture
 
Synonyms:
3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-1-propanone
3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
b-hydroxypropiovanillone
1-propanone, 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-
 propiophenone, 3,4'-dihydroxy-3'-methoxy-
 

Articles:

PubMed:[Chemical consitituents from root of Isatis indigotica].
PubMed:Sphingobium sp. SYK-6 LigG involved in lignin degradation is structurally and biochemically related to the glutathione transferase ω class.
PubMed:[Study on the chemical constituents of the roots of Dendropanax chevalieri].
PubMed:Phenolic constituents from the heartwood of Artocapus altilis and their tyrosinase inhibitory activity.
PubMed:Characterization of the third glutathione S-transferase gene involved in enantioselective cleavage of the β-aryl ether by Sphingobium sp. strain SYK-6.
PubMed:[Isoprenoids and phenylpropanoids from Saussurea deltoidea].
PubMed:Identification of three alcohol dehydrogenase genes involved in the stereospecific catabolism of arylglycerol-beta-aryl ether by Sphingobium sp. strain SYK-6.
PubMed:[Studies on chemical constituents from stem bark of Trewia nudiflora].
PubMed:Roles of the enantioselective glutathione S-transferases in cleavage of beta-aryl ether.
PubMed:Metabolism of Lignin Model Compounds of the Arylglycerol-beta-Aryl Ether Type by Pseudomonas acidovorans D(3).
 
Notes:
None found
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