Sigma-Aldrich C1251 (+)-Catechin hydrate ≥98% (HPLC), powder 5 gr
Marka
Stok Kodu
LB.SA.C1251-5G
Kısa Bilgi
Synonym(s): (+)-Cyanidol-3, (2R,3S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-1(2H)-benzopyran-3,5,7-triol Empirical Formula (Hill Notation): C15H14O6 · xH2O CAS Number: 225937-10-0 Molecular Weight: 290.27 (anhydrous basis) Beilstein: 3595244 EC Number: 205-825-1 MDL number: MFCD00150865 PubChem Substance ID: 57653982
Bilgi
CAS Number: 225937-10-0
Sigma-Aldrich C1251 (+)-Catechin hydrate ≥98% (HPLC), powder 5 gr |
Synonym(s): (+)-Cyanidol-3, (2R,3S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-1(2H)-benzopyran-3,5,7-triol Empirical Formula (Hill Notation): C15H14O6 · xH2O CAS Number: 225937-10-0 Molecular Weight: 290.27 (anhydrous basis) Beilstein: 3595244 EC Number: 205-825-1 MDL number: MFCD00150865 PubChem Substance ID: 57653982 |
PROPERTIES
Quality Level 200
Assay ≥98% (HPLC) form powder color yellow to yellow with tan cast mp 175-177 °C (anhydrous) (lit.) solubility ethanol: 50 mg/mL storage temp. 2-8°C SMILES string [H]O[H].O[C@H]1Cc2c(O)cc(O)cc2O[C@@H]1c3ccc(O)c(O)c3 InChI 1S/C15H14O6.H2O/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-5,13,15-20H,6H2;1H2/t13-,15+;/m0./s1 InChI key OFUMQWOJBVNKLR-NQQJLSKUSA-N DESCRIPTION General description Catechins are phytochemicals, richly present in black grapes, peaches, strawberries and broad beans. Catechins occur in various forms such as catechins, epicatechin, epicatechin gallate, epigallocatechin and epigallocatechin gallate.[1] Application (+)-Catechin hydrate has been used: as a polyphenol standard in the determination of total polyphenols in the by-products of red wine[2] as an additive to study its effects on in vitro methane production and substrate degradation in a triple-fed batch approach[3] as a substrate to determine the activity of pure L. plantarum CECT 748T 14 recombinant tannase on catechin[4] Biochem/physiol Actions An antioxidant flavonoid of plant origin; a free radical scavenger, preventing free radical-mediated damage in a variety of biological systems. For example, at physiological pH catechin suppressed DNA strand breaks by hydroxyl radicals. It has also been shown to prevent human plasma oxidation. It delayed the consumption of endogenous lipid-soluble antioxidants and inhibited lipid oxidation. Catechin may also function as an inhibitor of fatty acid synthase. |