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· · COA & SDS available for every product · Same-day shipping on in-stock items Rhapontin - ≥98% , CAS No.155-58-8
Synonyms
BSPBio_002946 | MFCD00010117 | N,N-Bis(trimethylsilyl)-1,4-butanediamine | Spectrum5_001757 | CHEBI:92176 | (2S,3R,4S,5S,6R)-2-(3-hydroxy-5-((E)-3-hydroxy-4-methoxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | GKAJCVFOJGXVIA-DXKBKAGUS
Storage
Store at 2-8°C,Protected from light
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
BSPBio_002946 | MFCD00010117 | N, N-Bis(trimethylsilyl)-1, 4-butanediamine | Spectrum5_001757 | CHEBI:92176 | (2S, 3R, 4S, 5S, 6R)-2-(3-hydroxy-5-((E)-3-hydroxy-4-methoxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3, 4, 5-triol | GKAJCVFOJGXVIA-DXKBKAGUS
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504759617 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504759617 Canonical Smiles COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O IUPAC Name (2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol InChIKey GKAJCVFOJGXVIA-DXKBKAGUSA-N INCHI 1S/C21H24O9/c1-28-16-5-4-11(8-15(16)24)2-3-12-6-13(23)9-14(7-12)29-21-20(27)19(26)18(25)17(10-22)30-21/h2-9,17-27H,10H2,1H3/b3-2+/t17-,18-,19+,20-,21-/m1/s1 Isomeric SMILES COC1=C(C=C(C=C1)/C=C/C2=CC(=CC(=C2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O PubChem CID 637213 Molecular Weight 420.41
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 Class Stilbenes Subclass Stilbene glycosides Intermediate Tree Nodes Not available Direct Parent Stilbene glycosides Alternative Parents Phenolic glycosides Hexoses O-glycosyl compounds Methoxyphenols Anisoles Styrenes Methoxybenzenes Phenoxy compounds 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Oxanes Secondary alcohols Acetals Oxacyclic compounds Polyols Primary alcohols Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Stilbene glycoside - Phenolic glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Styrene - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Oxane - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Ether - Polyol - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Primary alcohol - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as stilbene glycosides. These are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton. External Descriptors Diphenyl ethers, biphenyls, dibenzyls and stilbenes 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 Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity heat sensitive;light sensitive Melt Point(°C) 239 °C Molecular Weight 420.400 g/mol XLogP3 0.500 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 6 Exact Mass 420.142 Da Monoisotopic Mass 420.142 Da Topological Polar Surface Area 149.000 Ų Heavy Atom Count 30 Formal Charge 0 Complexity 559.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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