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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 22(R)-Hydroxycholesterol - ≥99% , CAS No.17954-98-2
Synonyms
(22R)-22-Hydroxycholesterol | CHEBI:67237 | C05502 | 22-alpha-hydroxycholesterol | DTXSID501313409 | BDBM20177 | (22R)-cholest-5-ene-3beta,22-diol | 22(r)hydroxycholesterol | 22(R)-Hydroxycholesterol | (1S,2R,5S,10S,11S,14R,15S)-14-[(2S,3R)-3-hydroxy-6-me
Shipped In
Ice chest + Ice pads
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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
(22R)-22-Hydroxycholesterol | CHEBI:67237 | C05502 | 22-alpha-hydroxycholesterol | DTXSID501313409 | BDBM20177 | (22R)-cholest-5-ene-3beta, 22-diol | 22(r)hydroxycholesterol | 22(R)-Hydroxycholesterol | (1S, 2R, 5S, 10S, 11S, 14R, 15S)-14-[(2S, 3R)-3-hydroxy-6-me
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504757606 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504757606 Sonrisas canónicas CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O IUPAC Name (3S,8S,9S,10R,13S,14S,17R)-17-[(2S,3R)-3-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol InChIKey RZPAXNJLEKLXNO-GFKLAVDKSA-N INCHI 1S/C27H46O2/c1-17(2)6-11-25(29)18(3)22-9-10-23-21-8-7-19-16-20(28)12-14-26(19,4)24(21)13-15-27(22,23)5/h7,17-18,20-25,28-29H,6,8-16H2,1-5H3/t18-,20-,21-,22+,23-,24-,25+,26-,27+/m0/s1 Isómeros SMILES C[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C)[C@@H](CCC(C)C)O WGK Alemania 3 Peso molecular 402.653 Reaxy-Rn 3435132 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3435132&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 Bile acids, alcohols and derivatives Intermediate Tree Nodes Hydroxy bile acids, alcohols and derivatives Direct Parent Dihydroxy bile acids, alcohols and derivatives Alternative Parents Cholesterols and derivatives 3-beta-hydroxysteroids 3-beta-hydroxy delta-5-steroids Delta-5-steroids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Cholesterol - Cholesterol-skeleton - Cholestane-skeleton - Dihydroxy bile acid, alcohol, or derivatives - 22-hydroxysteroid - Hydroxysteroid - 3-hydroxy-delta-5-steroid - 3-beta-hydroxysteroid - 3-hydroxysteroid - 3-beta-hydroxy-delta-5-steroid - Delta-5-steroid - Cyclic alcohol - Secondary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic homopolycyclic compound Descripción This compound belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. These are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups. External Descriptors Cholesterol 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) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 402.700 g/mol XLogP3 7.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 5 Exact Mass 402.35 Da Monoisotopic Mass 402.35 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 29 Formal Charge 0 Complexity 624.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 9 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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