89061
Eriodictyol
analytical standard
Synonyme(s) :
3·,4·,5,7-Tetrahydroxyflavanone
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About This Item
Formule empirique (notation de Hill):
C15H12O6
Numéro CAS:
Poids moléculaire :
288.25
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24
Produits recommandés
Qualité
analytical standard
Niveau de qualité
Pureté
≥98.0% (HPLC)
Durée de conservation
limited shelf life, expiry date on the label
Technique(s)
HPLC: suitable
gas chromatography (GC): suitable
Impuretés
≤5.0% water
Application(s)
food and beverages
Format
neat
InChI
1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m1/s1
Clé InChI
SBHXYTNGIZCORC-CYBMUJFWSA-N
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Description générale
Eriodictyol is a naturally occurring flavonoid found in citrus fruits. It can be isolated from the chinese herb, Dracocephalum rupestre. It may possess antioxidant activity.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Conditionnement
Bottomless glass bottle. Contents are inside inserted fused cone.
Autres remarques
This compound is commonly found in plants of the genus: mentha silybum thymus
For this product we use the non-stereospecific CAS number. It is expected that the natural enantiomer is predominant, however the substance is prone to racemization in solution. The product is therefore not specified stereospecifically and is only recommended to be used for non-stereospecific analysis.
Produits recommandés
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
The flavonoid, eriodictyol, induces long-term protection in ARPE-19 cells through its effects on Nrf2 activation and phase 2 gene expression
Johnson J, et al.
Investigative Ophthalmology & Visual Science, 50, 2398-2406 (2009)
S Ogata et al.
Bioscience, biotechnology, and biochemistry, 64(5), 1075-1078 (2000-07-06)
The flavonoid from lemon fruit (Citrus limon BURM. f.) and its metabolites, particularly eriodictyol, 3,4-dihydroxyhydrocinnamic acid, and phloroglucinol had the function of DNA fragmentation in HL-60 cells when analyzed by flow cytometry. An apoptotic DNA ladder and chromatin condensation were
B A 'T Hart et al.
Chemico-biological interactions, 73(2-3), 323-335 (1990-01-01)
The mechanism by which (a panel of) flanonoids inhibit the production of luminol-dependent chemiluminescence (CLlum) by activated human neutrophils is subject to this study. CLlum is frequently used as a bio-assay to quantify the effect of xenobiotics on the production
C Huang et al.
Xenobiotica; the fate of foreign compounds in biological systems, 39(4), 312-322 (2009-04-08)
Dietary flavonoids catechin, epicatechin, eriodictyol, and hesperetin were investigated as substrates and inhibitors of human sulfotransferases (hSULTs). Purified recombinant proteins and human intestine cytosol were used as enzyme sources. hSULT1A1 and hSULT1A3 as well as human intestine cytosol can catalyse
Eung-Ryoung Lee et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 27(5), 513-524 (2011-06-22)
Although flavonoids exhibit a variety of beneficial biological activities, the exact molecular mechanism of the cellular effects is still not fully explained. In this study, we investigated the molecular mechanism of cytoprotective effect of eriodictyol in UV-irradiated keratinocytes. We found
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