MORIN

MORIN
  • CAS No.:480-16-0
Other grades of this product :
MORIN Basic information
Product Name:MORIN
Synonyms:TIMTEC-BB SBB008853;MORIN;FUSTIC;CI 75660;CI NO 75660;3,5,7,2',4'-PENTAHYDROXYFLAVONE;2',3,4',5,7-PENTAHYDROXYFLAVONE;2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4h-1-benzopyran-4-on
CAS:480-16-0
MF:C15H10O7
MW:302.24
EINECS:207-542-9
Product Categories:Inhibitors;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Flavanols;Biochemistry;Flavonoids
Mol File:480-16-0.mol
MORIN Chemical Properties
Melting point 299-300 °C (dec.)(lit.)
Boiling point 363.28°C (rough estimate)
density 1.3616 (rough estimate)
refractive index 1.4790 (estimate)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility methanol: 50 mg/mL
Colour Index 75660
pka6.30±0.40(Predicted)
form powder
color yellow
Water Solubility 0.25g/L(20 ºC)
Merck 6269
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyYXOLAZRVSSWPPT-UHFFFAOYSA-N
LogP1.27-1.54 at 37℃ and pH7.4
CAS DataBase Reference480-16-0(CAS DataBase Reference)
EPA Substance Registry SystemMorin (480-16-0)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-25
Safety Statements 26-36-45
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
RTECS LK8749000
8-10-23
HS Code 29329990
ToxicityLD50 intraperitoneal in mouse: 555mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
MORIN Usage And Synthesis
Chemical Propertiesyellow to brown powder
UsesP450 and ATPase inhibitor
UsesMorin is a natural pentahydroxyflavonol with antioxidant activity. It reduces CD36 expression and oxLDL uptake in U937-derived macrophages, inhibits PIM-1 kinase in vitro (IC50 = 2.7 μM), and reduces the activity of cytochrome P450 isoform 3A4 in liver microsomes. Through these and other actions, morin has anti-oxidant, anti-inflammatory, and other actions in animal models.[Cayman Chemical]
UsesMorin is a polyphenolic flavonoid with radical scavenging ability. In addition it maintains the potential for suppression of lipopolysaccharide-induced neuroinflammation.
DefinitionChEBI: A pentahydroxyflavone that is 7-hydroxyflavonol bearing three additional hydroxy substituents at positions 2' 4' and 5.
Safety ProfileModerately toxic by intraperitoneal route. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.
Purification MethodsStir morin at room temperature with ten times its weight of absolute EtOH, then leave overnight to settle. Filter it off, and evaporate under a heat lamp to one-tenth its volume. An equal volume of water is added, and the precipitated morin is filtered off, dissolved in the minimum amount of EtOH and again precipitated with an equal volume of water. The precipitate is filtered off, washed with water and dried at 110o for 1hour (yield ca 2.5%.). [Perkins & Kalkwarf Anal Chem 28 1989 1956.] It complexes with W and Zr. [Beilstein 18 H 239, 18 III/IV 3468, 18/5 V 492.]
MORIN Preparation Products And Raw materials

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