Estrone

Estrone structural formula

CAS Number53-16-7
Molecular FormulaC18H22O2
Molecular Weight270.373
InChI KeyDNXHEGUUPJUMQT-CBZIJGRNSA-N
LogP3.13
Synonyms
  • Estrone
  • 3-Hydroxyestra-1,3,5(10)-trien-17-one
  • Estra-1,3,5(10)-trien-17-one, 3-hydroxy-
  • 53-16-7
  • E1
  • 3-08-00-01171
  • Estra-1,3,5(10)-trien-17-one, 3-hydroxy-
  • (+)-Estrone
  • 1,3,5(10)-Estratrien-3-ol-17-one
  • 3-Hydroxy-17-keto-estra-1,3,5-triene
  • 3-Hydroxyestra-1,3,5(10)-trien-17-one
  • 3-Hydroxyestra-1,3,5(10)-triene-17-one
  • 3-Hydroxyoestra-1,3,5(10)-trien-17-one
  • Aquacrine
  • Crinovaryl
  • Cristallovar
  • Crystogen
  • Destrone
  • Disynformon
  • Endofolliculina
  • estrona
  • Estrovarin
  • Estrugenone
  • Estrusol
  • Femestrone Inj.
  • Femestrone injection
  • Femidyn
  • Fermidyn
  • Folikrin
  • Folipex
  • Folisan
  • Follestrine
  • Follestrol
  • Follicular hormone
  • Folliculin
  • Folliculinum
  • Follicunodis
  • Follidrin
  • Glandubolin
  • Hiestrone
  • Hormofollin
  • Hormovarine
  • Kestrone
  • Ketodestrin
  • Ketohydroxyestrin
  • Menagen
  • Menformon
  • NSC 9699
  • Oestrin
  • Oestroform
  • Oestrone
  • Oestroperos
  • Ovifollin
  • Perlatan
  • Solliculin
  • Theelin
  • Thelestrin
  • Thelykinin
  • Thynestron
  • Tokokin
  • Wynestron
  • Δ1,3,5(10)-Estratrien-3-ol-17-one
  • BRN 1915077
  • EINECS 200-164-5
  • delta-1,3,5-Estratrien-3beta-ol-17-one
  • delta-1,3,5-estratrien-3-beta-ol-17-one
  • Estrone-A
  • Fem-O-Gen
  • Folliculine
  • Folliculine benzoate
  • Hormestrin
  • 3-Hydroxy-17-keto-oestra-1,3,5-triene
  • 3-Hydroxy-oestra-1,3,5(10)-trien-17-one
  • Ketohydroxy-estratriene
  • Ketohydroxyoestrin
  • Mestronaq
  • 1,3,5(10)-Oestratrien-3-ol-17-one
  • delta-1,3,5-Oestratrien-3beta-ol-17-one
  • delta-1,3,5-oestratrien-3-beta-ol-17-one
  • Oestronum
  • Unden
  • Estrogenic substance
  • Natural estrogenic substance-estrone
  • Estronum
  • UNII-2DI9HA706A
  • (1S,10R,11S,15S)-5-hydroxy-15-methyltetracyclo[8.7.0.02,7.011,15]heptadeca-2,4,6-trien-14-one
  • (8R,9S,13S,14S)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one
  • D1,3,5(10)-Estratrien-3-ol-17-one
  • 37242-41-4

Applications:

HPLC Separation of Estrone

September 9, 2015

 

Estrone, also known at oestrone and E1 is a naturally occurring estrogen which is the predominant estrogen in postmenopausal women. It can be found in its long-lived form estrone sulfate. In certain scenarios estrone can be a carcinogen and causes breast pain, nausea, headaches and leg cramps. It was separated on both Obelisc R and Primesep 100 which have unique modes of retention. Method is LC/MS compatible and useful for separating a number of pesticides.

 

Condition 1

Column Obelisc R, 2.1×150 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 25-70%, 15 min
Buffer Gradient AmAc pH 3.0- 30-60 mM, 15 min
Flow Rate 0.4 ml/min
Detection UV, 270 nm

 

Condition 2

Column Obelisc R, 2.1×150 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 10-70%, 15 min
Buffer Gradient AmAc pH 3.0- 20-60 mM, 15 min
Flow Rate 0.4 ml/min
Detection UV, 270 nm

 

Condition 3

Column Primesep 100, 2.1×150 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 10-70%, 15 min
Buffer Gradient AmAc pH 3.0- 20-60 mM, 15 min
Flow Rate 0.4 ml/min
Detection UV, 270 nm

 

Description

Class of Compounds
 Hormone,  Hydrophobic, Ionizable
Analyzing Compounds Estrone

 

Application Column

Obelisc R

SIELC has developed the Obelisc™ columns, which are mixed-mode and utilize Liquid Separation Cell technology (LiSC™). These cost-effective columns are the first of their kind to be commercially available and can replace multiple HPLC columns, including reversed-phase (RP), AQ-type reversed-phase, polar-embedded group RP columns, normal-phase, cation-exchange, anion-exchange, ion-exclusion, and HILIC (Hydrophilic Interaction Liquid Chromatography) columns. By controlling just three orthogonal method parameters - buffer concentration, buffer pH, and organic modifier concentration - users can adjust the column properties with pinpoint precision to separate complex mixtures.

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Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

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Application Analytes:
Estrone

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.