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Merck

45714

Sigma-Aldrich

Eriocitrin

≥98.0% (HPLC)

Synonym(e):

(S)-3′,4′,5,7-Tetrahydroxy-flavanon-7-[6-O-(α-L-rhamnopyranosyl)-β-D-glucopyranosid], Eriodictiosid, Eriodictyol-7-O-rutinosid

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About This Item

Empirische Formel (Hill-System):
C27H32O15
CAS-Nummer:
Molekulargewicht:
596.53
Beilstein:
1304401
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352205
PubChem Substanz-ID:
NACRES:
NA.47

Assay

≥98.0% (HPLC)

Form

solid

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES String

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3cc(O)c4C(=O)C[C@H](Oc4c3)c5ccc(O)c(O)c5)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C27H32O15/c1-9-20(32)22(34)24(36)26(39-9)38-8-18-21(33)23(35)25(37)27(42-18)40-11-5-14(30)19-15(31)7-16(41-17(19)6-11)10-2-3-12(28)13(29)4-10/h2-6,9,16,18,20-30,32-37H,7-8H2,1H3/t9-,16-,18+,20-,21+,22+,23-,24+,25+,26+,27+/m0/s1

InChIKey

OMQADRGFMLGFJF-MNPJBKLOSA-N

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Biochem./physiol. Wirkung

Flavone glycoside found in lemon. Administration prior to acute exercise helped to maintain the redox status of liver glutathione. Without eriocitrin, it shifts markedly toward oxidized form.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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