beta-hydroxypropiovanillone

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

CAS: 2196-18-1 C10 H12 O4 MW: 196.20244000

Identification

Namebeta-hydroxypropiovanillone
IUPAC3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
CAS Number2196-18-1
FDA UNIIM22UI268J1
Molecular FormulaC10 H12 O4
Molecular Weight196.20244000
Nikkaji NumberJ102.027G
XlogP3-0.20 (est)

Regulatory

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)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for beta-hydroxypropiovanillone usage levels up tonot for fragrance use.
Recommendation for beta-hydroxypropiovanillone flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

ligusticum porteri

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- 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).