40043
Matairesinol
≥85% (HPLC)
Synonym(s):
(αR,βR)-α,β-Bis(4-hydroxy-3-methoxybenzyl)butyrolactone
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About This Item
Empirical Formula (Hill Notation):
C20H22O6
CAS Number:
Molecular Weight:
358.39
Beilstein:
7826317
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.21
Quality Level
Assay
≥85% (HPLC)
storage temp.
2-8°C
SMILES string
COc1cc(C[C@H]2COC(=O)[C@@H]2Cc3ccc(O)c(OC)c3)ccc1O
InChI
1S/C20H22O6/c1-24-18-9-12(3-5-16(18)21)7-14-11-26-20(23)15(14)8-13-4-6-17(22)19(10-13)25-2/h3-6,9-10,14-15,21-22H,7-8,11H2,1-2H3/t14-,15+/m0/s1
InChI key
MATGKVZWFZHCLI-LSDHHAIUSA-N
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Other Notes
Matairesinol, a phytoestrogen is employed as dietary supplement leading to metabolites with estrogenic properties; HPLC determination of matairesinol
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tanja Kraushofer et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 777(1-2), 61-66 (2002-09-25)
A HPLC method coupled with coulometric electrode array detection for the determination of matairesinol in flax seed is described. The defatted sample was spiked with bisphenol A (internal standard), refluxed for 75 min in a mixture of ethanol-bidistilled water-12 M
L.P. Meagher, G.R. Beecher
J. Food Compos. Anal., 13, 935-935 (2000)
Baoru Yang et al.
Journal of agricultural and food chemistry, 54(21), 8065-8070 (2006-10-13)
Sea buckthorn (Hippophaë rhamnoides) seeds, berries, and berry fractions are often used as sources of bioactive ingredients for health products. The aim of the present study was to analyze lignans in these fractions of sea buckthorn. Secoisolariciresinol and matairesinol in
Parduman R Sharma et al.
Phytotherapy research : PTR, 22(12), 1587-1594 (2008-12-11)
AP9-cd, a synergistic lignan mixture from Cedrus deodara (Pinaceae) consisting of (-)-wikstromal, (-)-matairesinol and dibenzyl butyrolactol, depicted cytotoxic effects against numerous human cancer cell lines reported previously. The aim of this study was to investigate the mechanism of cell death
Johanna W Lampe et al.
Journal of AOAC International, 89(4), 1174-1181 (2006-08-19)
Phytoestrogens occur naturally in plants and are structurally similar to mammalian estrogens. The lignans are a class of phytoestrogen and can be metabolized to the biologically active enterolignans, enterodiol, and enterolactone by a consortium of intestinal bacteria. Secoisolariciresinol diglucoside (SDG)
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