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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel Ononin - ≥97%(HPLC) , CAS No.486-62-4
Synonyms
2-(2,2-Dicyclohexylethyl)piperidine acid maleate | FORMONONETIN 7-O-.BETA.-D-GLUCOSIDE | Z0Z637970U | 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-methoxyphenyl)- | AS-72370 | CHEBI:7775 | 7Beta-(Glucosyloxy)Formonometin | Fomononetin-7-O-gluc
Storage
Room temperature,Argon charged
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Why this grade ≥97%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyme
2-(2,2-Dicyclohexylethyl)piperidine acid maleate | FORMONONETIN 7-O-.BETA.-D-GLUCOSIDE | Z0Z637970U | 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-methoxyphenyl)- | AS-72370 | CHEBI:7775 | 7Beta-(Glucosyloxy)Formonometin | Fomononetin-7-O-gluc
Spezifikationen & Reinheit
≥97%(HPLC)
Biochemische und physiologische Mechanismen
A isoflavone glucoside found in soybean, kudzu, and the Chinese medicinal herb, Radix astragali (RA). RA is a supplement taken to improve "energy." It may act by inducing erythropoietin expression.
Storage
Room temperature,Argon charged
Namen und Kennungen Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504758789
Kanonisches Lächeln
COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O
IUPAC Name
3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
InChIKey
MGJLSBDCWOSMHL-MIUGBVLSSA-N
INCHI
1S/C22H22O9/c1-28-12-4-2-11(3-5-12)15-10-29-16-8-13(6-7-14(16)18(15)24)30-22-21(27)20(26)19(25)17(9-23)31-22/h2-8,10,17,19-23,25-27H,9H2,1H3/t17-,19-,20+,21-,22-/m1/s1
Isomere SMILES
COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14609706&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides Klasse Isoflavonoids Subclass Isoflavonoid O-glycosides Intermediate Tree Nodes Not available Direct Parent Isoflavonoid O-glycosides Alternative Parents 4'-O-methylisoflavones Isoflavones Phenolic glycosides Hexoses Chromones O-glycosyl compounds Anisoles Methoxybenzenes Phenoxy compounds Alkyl aryl ethers Pyranones and derivatives Oxanes Heteroaromatic compounds Secondary alcohols Acetals Polyols Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Isoflavonoid-7-o-glycoside - Isoflavonoid o-glycoside - 4p-o-methylisoflavone - Isoflavone - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Pyranone - Alkyl aryl ether - Pyran - Monocyclic benzene moiety - Oxane - Monosaccharide - Benzenoid - Heteroaromatic compound - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Ether - Polyol - Organic oxygen compound - Alcohol - Primary alcohol - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. External Descriptors isoflavones - Isoflavonoids Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Empfindlichkeit Moisture Sensitive Schmelzpunkt (°C) 243 °C(dec.) Molekulargewicht 430.400 g/mol XLogP3 1.000 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 5 Exact Mass 430.126 Da Monoisotopic Mass 430.126 Da Topological Polar Surface Area 135.000 Ų Heavy Atom Count 31 Formal Charge 0 Complexity 659.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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