datiscetin

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3,5,7-trihydroxy-2-(2-hydroxyphenyl)-4-benzopyrone

CAS: 480-15-9 C15 H10 O6 MW: 286.23990000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers

Identification

Namedatiscetin
IUPAC3,5,7-trihydroxy-2-(2-hydroxyphenyl)chromen-4-one
CAS Number480-15-9
EINECS207-541-3
FDA UNIIM8C5EH705I
Molecular FormulaC15 H10 O6
Molecular Weight286.23990000
MDL NumberMFCD00017307
Nikkaji NumberJ6.162J
Beilstein0039982
XlogP31.90 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 563.88 °C. @ 760.00 mm Hg (est)
Flash Point 426.00 °F. TCC ( 218.90 °C. ) (est)
logP (o/w) 3.429 (est)
Soluble in water, 1191 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 datiscetin usage levels up tonot for fragrance use.
Recommendation for datiscetin flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

4H-1- benzopyran-4-one, 3,5,7-trihydroxy-2-(2-hydroxyphenyl)- 2',3,5,7- tetrahydroxyflavone 3,5,7,2'- tetrahydroxyflavone 3,5,7- trihydroxy-2-(2-hydroxyphenyl)-4-benzopyrone 3,5,7- trihydroxy-2-(2-hydroxyphenyl)-4H-1-benzopyran-4-one 3,5,7- trihydroxy-2-(2-hydroxyphényl)-4h-chromén-4-one 3,5,7- trihydroxy-2-(2-hydroxyphenyl)chromen-4-one PubMed: Indirect activation of the SV23 and SV24 splice variants of human constitutive androstane receptor: analysis with 3-hydroxyflavone and its analogues. PubMed: Small molecule inhibitors of the HPV16-E6 interaction with caspase 8. PubMed: Kinetic and stoichiometric assessment of the antioxidant activity of flavonoids by electron spin resonance spectroscopy. PubMed: Fungitoxic phenols from carnation (Dianthus caryophyllus) effective against Fusarium oxysporum f. sp. dianthi. PubMed: Activity of plant flavonoids against antibiotic-resistant bacteria. PubMed: Inhibitory effects of phenolic compounds on CCl4-induced microsomal lipid peroxidation. PubMed: Structure-activity relationships of polymethoxyflavones and other flavonoids as inhibitors of non-enzymic lipid peroxidation. PubMed: Superoxide scavenging properties of flavonoids in a non-enzymic system.