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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 16-Epiestriol - ≥90% , CAS No.547-81-9
Synonyms
8XZ32LI44K | Estra-1,3,5(10)-triene-3,16.beta.,17.beta.-triol | NSC-758892 | Epiestriol | Q24897913 | NSC 26646 | Estra-1,3,5(10)-triene-3,16beta,17beta-triol | Estra-1,3,5(10)-triene-3,16beta,17beta-triol (16-epi-Estriol) | SCHEMBL221084 | NSC 758892 | U
Shipped In
Hielera + almohadillas de hielo
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Why this grade ≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a -20°C Ships Hielera + almohadillas de hielo 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general el 16-Epiestriol es un metabolito del Estradiol.
Specifications Sinónimos
8XZ32LI44K | Estra-1, 3, 5(10)-triene-3, 16.beta., 17.beta.-triol | NSC-758892 | Epiestriol | Q24897913 | NSC 26646 | Estra-1, 3, 5(10)-triene-3, 16beta, 17beta-triol | Estra-1, 3, 5(10)-triene-3, 16beta, 17beta-triol (16-epi-Estriol) | SCHEMBL221084 | NSC 758892 | U
Especificaciones y pureza
≥90%
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Pubchem Sid 488184184 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184184 Sonrisas canónicas CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)O IUPAC Name (8R,9S,13S,14S,16S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,16,17-triol InChIKey PROQIPRRNZUXQM-ZMSHIADSSA-N INCHI 1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16+,17+,18+/m1/s1 Isómeros SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@@H]([C@@H]2O)O)CCC4=C3C=CC(=C4)O Peso molecular 288.38 Reaxy-Rn 2057375 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2057375&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 Steroids and steroid derivatives Subclass Estrane steroids Intermediate Tree Nodes Not available Direct Parent Estrogens and derivatives Alternative Parents 3-hydroxysteroids 17-hydroxysteroids 16-beta-hydroxysteroids Phenanthrenes and derivatives Tetralins 1-hydroxy-2-unsubstituted benzenoids Secondary alcohols Cyclic alcohols and derivatives 1,2-diols Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Estrogen-skeleton - 3-hydroxysteroid - 17-hydroxysteroid - 16-hydroxysteroid - 16-beta-hydroxysteroid - Hydroxysteroid - Phenanthrene - Tetralin - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Cyclic alcohol - Secondary alcohol - 1,2-diol - Polyol - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Aromatic homopolycyclic compound Descripción This compound belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane. External Descriptors C18 steroids (estrogens) and derivatives 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) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in Methanol Punto de fusión (°C) 265-2680°C (lit.) Peso molecular 288.400 g/mol XLogP3 2.500 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 0 Exact Mass 288.173 Da Monoisotopic Mass 288.173 Da Topological Polar Surface Area 60.700 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 411.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 6 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
Citations of This Product Referencias 1. Yingchao Liu, Jiahui Bai, Xiaoxia Dong, Yuqi Cao, Mingmai Bao, Yingjie Lu, Hui Zeng, Lixing Zhan, Yinlong Guo. (2024) Online Charge-Generation Derivatization by Electrochemical Radical Cations of Thianthrene: Mass Spectrometry Imaging of Estrogens in Biological Tissues. ANALYTICAL CHEMISTRY, [PMID:39031066 ] [10.1021/acs.analchem.4c02086 ]
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