cirsimaritin
- CAS NO.：6601-62-3
- Empirical Formula: C17H14O6
- Molecular Weight: 314.29
- MDL number: MFCD00238561
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-06-03 11:24:09
What is cirsimaritin?
The Uses of cirsimaritin
Cirsimaritin is a flavonoid obtained from Cirsium japonicum var. maackii pappus and is effective as an anti-inflammatory agent as well as antioxidant.
Definition
ChEBI: A dimethoxyflavone that is flavone substituted by methoxy groups at positions 6 and 7 and hydroxy groups at positions 5 and 4' respectively.
Properties of cirsimaritin
| Melting point: | 257 °C |
| Boiling point: | 563.6±50.0 °C(Predicted) |
| Density | 1.402±0.06 g/cm3(Predicted) |
| storage temp. | -20°C |
| solubility | DMSO: 10 mM |
| form | A solid |
| pka | 6.34±0.40(Predicted) |
| color | Light yellow to light brown |
Safety information for cirsimaritin
| Signal word | Danger |
| Pictogram(s) |
 Skull and Crossbones Acute Toxicity GHS06  Environment GHS09 |
| GHS Hazard Statements |
H301:Acute toxicity,oral H410:Hazardous to the aquatic environment, long-term hazard |
| Precautionary Statement Codes |
P273:Avoid release to the environment. |
Computed Descriptors for cirsimaritin
New Products
AMino-(3-Methylphenyl)-acetic acid 4-Fluorophenylglycine 3-AMINO-3-(2-CHLORO-PHENYL)-PROPIONIC ACID Dimedone 1-N-Boc-3-(aminoethyl)azetidine 1-Boc-3-(cyanomethyl)azetidine 2-Amino-3-Bromopyridine 2-Amino-3-Bromo-5-Nitropyridine Pyridine-N-oxide 4-Hydroxypyridine 2-Hydroxy-6-Picoline 5-Bromo-2-Chloropyridine 2-Amino-4-phenyl-thiazole 4-Chloro-2-methyl quinoline N-(4-Bromophenyl)-2-chloroacetamide 2-Aminobenzo[d]thiazol-4-ol 4-Nitrobenzenesulfonohydrazide 1-(3-Hydroxyphenyl)-2-thiourea Phenyl-boronic acid-d5 10,11-Dihdyro-10-oxo-5H-dibenz[b,f]azepine-5-carboxamide-d4 4-(4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 2,6-dimethoxyphenol 2-(2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)-4-methylpyrimidine N-(4-(4-(4-Methoxyphenyl)piperazin-1-yl)phenyl)hydrazinecarboxamideRelated products of tetrahydrofuran
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