16α-Hydroxy Estrone - ≥95% , CAS No.566-76-7

CAS: 566-76-7 Cat. No.: H336200 Peso molecular: 286.37 Número EC: 637-216-5
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
3,16-Dihydroxyestra-1,3,5(10)-trien-17-one # | A-Hydroxyestrone | 3,16alpha-Dihydroxyestra-1,3,5(10)-trien-17-one (16alpha-Hydroxyestrone) | (16.ALPHA.)-3,16-DIHYDROXYESTRA-1(10),2,4-TRIEN-17-ONE | MS-24094 | 16??-Hydroxyestrone | 16alpha-Hydroxyestrone |
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Size
USA
Alemania (EU)*
Price
Qty
1mg
H336200-1mg
1 Disponible

457,90US$

534,90US$
Guardar 77,00 US$ (14.40%)
5mg
H336200-5mg
Fabricado bajo pedido · 8–12 semanas

1.567,90US$

1.867,90US$
Guardar 300,00 US$ (16.06%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

16α-Hydroxy Estrone is a major Estradiol metabolite.

Specifications

Sinónimos
3,16-Dihydroxyestra-1,3,5(10)-trien-17-one # | A-Hydroxyestrone | 3,16alpha-Dihydroxyestra-1,3,5(10)-trien-17-one (16alpha-Hydroxyestrone) | (16.ALPHA.)-3,16-DIHYDROXYESTRA-1(10),2,4-TRIEN-17-ONE | MS-24094 | 16??-Hydroxyestrone | 16alpha-Hydroxyestrone |
Especificaciones y pureza
≥95%
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.
Pureza
≥95%
Nombres e identificadores
Pubchem Sid528754876
Sonrisas canónicasCC12CCC3C(C1CC(C2=O)O)CCC4=C3C=CC(=C4)O
IUPAC Name(8R,9S,13S,14S,16R)-3,16-dihydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one
InChIKeyWPOCIZJTELRQMF-QFXBJFAPSA-N
INCHI1S/C18H22O3/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/h3,5,8,13-16,19-20H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,18+/m1/s1
Isómeros SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H](C2=O)O)CCC4=C3C=CC(=C4)O
Peso molecular 286.37
Reaxy-Rn 25855869
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25855869&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClaseSteroids and steroid derivatives
SubclassEstrane steroids
Intermediate Tree Nodes Not available
Direct ParentEstrogens and derivatives
Alternative Parents 3-hydroxysteroids  17-oxosteroids  16-alpha-hydroxysteroids  Phenanthrenes and derivatives  Tetralins  1-hydroxy-2-unsubstituted benzenoids  Secondary alcohols  Ketones  Cyclic alcohols and derivatives  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Estrogen-skeleton - 3-hydroxysteroid - Hydroxysteroid - 17-oxosteroid - Oxosteroid - 16-alpha-hydroxysteroid - 16-hydroxysteroid - Phenanthrene - Tetralin - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Cyclic alcohol - Secondary alcohol - Ketone - Carbonyl group - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homopolycyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (787 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeFechaArticulo
C23161169Certificate of AnalysisDec 13, 2022 H336200
C2527177Certificate of AnalysisDec 13, 2022 H336200
Propiedades químicas y físicas
Punto de fusión (°C)209-211° C
Peso molecular286.400 g/mol
XLogP32.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass286.157 Da
Monoisotopic Mass286.157 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count21
Formal Charge0
Complexity448.000
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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