5,7,4'-trimethyl apigenin

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4H-1-benzenopyran-4-one, 5,7-dimethoxy-2-(4-methoxyphenyl)-

CAS: 5631-70-9 C18 H16 O5 MW: 312.32152000

Identification

Name5,7,4'-trimethyl apigenin
IUPAC5,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one
CAS Number5631-70-9
FDA UNIIF50JU8E74U
Molecular FormulaC18 H16 O5
Molecular Weight312.32152000
Nikkaji NumberJ145.241J
XlogP32.20 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 506.50 °C. @ 760.00 mm Hg (est)
Flash Point 438.00 °F. TCC ( 225.50 °C. ) (est)
logP (o/w) 3.530 (est)
Soluble in water, 6.512 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 5,7,4'-trimethyl apigenin usage levels up tonot for fragrance use.
Recommendation for 5,7,4'-trimethyl apigenin flavor usage levels up tonot for flavor use.

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5631-70-9 4',5,7-Trimethoxyflavone 98%
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Potential Uses

None Found

Natural Occurrence

mandarin peel orange pericarp orthosiphon spicatus

Synonyms

apigenin trimethyl ether apigenin-4',5,7-trimethyl ether apigenin-4',5,7-trimethylether 4H-1- benzenopyran-4-one, 5,7-dimethoxy-2-(4-methoxyphenyl)- 5,7- dimethoxy-2-(4-methoxyphenyl)-4H-1-benzenopyran-4-one 5,7- dimethoxy-2-(4-methoxyphenyl)chromen-4-one 4',5,7- trimethoxyflavone 4',5,7- trimethyl-apigenin 5,7,4'- trimethylapigenin PubMed: Effects of the natural flavone trimethylapigenin on cardiac potassium currents. PubMed: Anticholinesterase activity of 7-methoxyflavones isolated from Kaempferia parviflora. PubMed: Activation of the CFTR Cl- channel by trimethoxyflavone in vitro and in vivo. PubMed: Bioactive compounds from Lippia javanica and Hoslundia opposita. PubMed: Lipophilic flavonoids from Orthosiphon spicatus prevent oxidative inactivation of 15-lipoxygenase.