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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Cycloastragenol - 10mM in DMSO , CAS No.78574-94-4
GRADE & PURITY 10mM in DMSO
Synonyms
9,19-CYCLOLANOSTANE-3,6,16,25-TETROL, 20,24-EPOXY-, (3.BETA.,6.ALPHA.,16.BETA.,20R,24S)- | CHEBI:71314 | Cyclogalegigenin | Q3979404 | A864051 | Astramembrangenin | J427.606J | (3beta,6alpha,16beta,20R,24S)-20,24-Epoxy-9,19-cyclolanostane-3,6,16,25-tetrol
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -80°C Ships Dry ice packs + Cold packs 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 Sinónimos
9, 19-CYCLOLANOSTANE-3, 6, 16, 25-TETROL, 20, 24-EPOXY-, (3.BETA., 6.ALPHA., 16.BETA., 20R, 24S)- | CHEBI:71314 | Cyclogalegigenin | Q3979404 | A864051 | Astramembrangenin | J427.606J | (3beta, 6alpha, 16beta, 20R, 24S)-20, 24-Epoxy-9, 19-cyclolanostane-3, 6, 16, 25-tetrol
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Protected from light, Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)O)C IUPAC Name (1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol InChIKey WENNXORDXYGDTP-UOUCMYEWSA-N INCHI 1S/C30H50O5/c1-24(2)20(33)8-11-30-16-29(30)13-12-26(5)23(28(7)10-9-21(35-28)25(3,4)34)18(32)15-27(26,6)19(29)14-17(31)22(24)30/h17-23,31-34H,8-16H2,1-7H3/t17-,18-,19-,20-,21-,22-,23-,26+,27-,28+,29-,30+/m0/s1 Isómeros SMILES C[C@]12CC[C@@]34C[C@@]35CC[C@@H](C([C@@H]5[C@H](C[C@H]4[C@@]1(C[C@@H]([C@@H]2[C@]6(CC[C@H](O6)C(C)(C)O)C)O)C)O)(C)C)O RTECS GX8265000 Peso molecular 490.73 Reaxy-Rn 42764296 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42764296&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 Lipids and lipid-like molecules Clase Prenol lipids Subclass Terpene glycosides Intermediate Tree Nodes Triterpene glycosides Direct Parent Triterpene saponins Alternative Parents Triterpenoids Cycloartanols and derivatives 6-hydroxysteroids 3-beta-hydroxysteroids 16-beta-hydroxysteroids Tetrahydrofurans Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives Molecular Framework Aliphatic heteropolycyclic compounds Substituents Triterpene saponin - Cycloartanol-skeleton - 9b,19-cyclo-lanostane-skeleton - Cycloartane-skeleton - Triterpenoid - 3-hydroxysteroid - 6-hydroxysteroid - Hydroxysteroid - 3-beta-hydroxysteroid - 16-beta-hydroxysteroid - 16-hydroxysteroid - Steroid - Tertiary alcohol - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Polyol - Ether - Dialkyl ether - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Aliphatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton. External Descriptors tetrol - oxolanes - pentacyclic triterpenoid - sapogenin 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.
Estructura 3D Objetivos asociados (humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Heat & light Sensitive Rotación específica [α] 49° (C=1.37,MeOH) Punto de fusión (°C) 241 °C Peso molecular 490.700 g/mol XLogP3 4.400 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 2 Exact Mass 490.366 Da Monoisotopic Mass 490.366 Da Topological Polar Surface Area 90.200 Ų Heavy Atom Count 35 Formal Charge 0 Complexity 916.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 12 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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