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 Method for Analysis of Estetrol, Estiol, Estrone, and Besta-Estradiol Without Buffer on Chromni Column

September 16, 2025

HPLC Method for Estrone, Estradiol, Estriol, Estetrol on Chromni™ by SIELC Technologies


High Performance Liquid Chromatography (HPLC) Method for Analysis of Estrone, Estradiol, Estriol, Estetrol

Estetrol is an estrogenic steroid hormone compound with the molecular formula C18H24O4.

Properties:
Appearance: Typically a white, odorless, powder.

Molecular weight: ~270.4 g/mol

Solubility: Soluble in water.

Uses: Production of contraceptives.

Estriol is an estrogenic steroid hormone compound with the molecular formula C18H24O3.

Properties:
Appearance: Typically a white, odorless, powder.

Molecular weight: ~288.4 g/mol

Solubility: Soluble in benzene, water, alcohol, and vegetable oils.

Uses: Hormone Replacement Therapy and similar medication.

Estrone is an synthetic estrogenic steroid hormone with the molecular formula C18H22O2.

Properties:
Appearance: Typically a white, odorless, crystals.

Molecular weight: ~270.4 g/mol

Solubility: Soluble in benzene, water, acetone, and vegetable oils.

Uses: Production of medication

Beta-Estradiol is an estrogenic steroid hormone compound with the molecular formula C18H24O2.

Properties:
Appearance: Typically a white, odorless, crystals.

Molecular weight: ~272.4 g/mol

Solubility: Soluble in ethanol, water, and vegetable oils.

Uses: Production of medication for treatment of menopausal symptoms

Estrone, Estradiol, Estriol, Estetrol can be retained and analyzed using the Chromni™ stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN). Detection is performed using UV.

ColumnChromni™, 4.6 x 150 mm, 3 µm, 100 A, dual ended
Mobile PhaseMeCN – 90%
BufferNone
Flow Rate1.0 ml/min
DetectionUV 280 nm

Class of CompoundsEstrogen
Analyzing CompoundsEstrone, Estradiol, Estriol, Estetrol

Application Column

Chromni™

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 3 µm
Pore Size: 100 A
Column options: dual ended

Add to cart
Application Analytes:
Estetrol
Estradiol
Estriol
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.

HPLC Method for Analysis of Estetrol, Estiol, Estrone, and Besta-Estradiol on Chromni Column

September 16, 2025

HPLC Method for Estrone, Estradiol, Estetrol, Estriol on Chromni™ by SIELC Technologies


High Performance Liquid Chromatography (HPLC) Method for Analysis of Estrone, Estradiol, Estetrol, Estriol

Estetrol is an synthetic organochlorine compound with the molecular formula C18H24O4.

Properties:
Appearance: Typically a white, odorless, powder.

Molecular weight: ~270.4 g/mol

Solubility: Soluble in water.

Uses: Production of contraceptives.

Estriol is an synthetic organochlorine compound with the molecular formula C18H24O3.

Properties:
Appearance: Typically a white, odorless, powder.

Molecular weight: ~288.4 g/mol

Solubility: Soluble in benzene, water, alcohol, and vegetable oils.

Uses: Hormone Replacement Therapy and similar medication.

Estrone is an synthetic organochlorine compound with the molecular formula C18H22O2.

Properties:
Appearance: Typically a white, odorless, crystals.

Molecular weight: ~270.4 g/mol

Solubility: Soluble in benzene, water, acetone, and vegetable oils.

Uses: Production of medication

Beta-Estradiol is an synthetic organochlorine compound with the molecular formula C18H24O2.

Properties:
Appearance: Typically a white, odorless, crystals.

Molecular weight: ~272.4 g/mol

Solubility: Soluble in ethanol, water, and vegetable oils.

Uses: Production of medication for treatment of menopausal symptoms

Estrone, Estradiol, Estetrol, Estriol can be retained and analyzed using the Chromni™ stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN), and ammonium formate. Detection is performed using UV.

ColumnChromni™, 4.6 x 150 mm, 3 µm, 100 A, dual ended
Mobile PhaseMeCN – 20%
BufferAmmonium Formate – 10mM
Flow Rate1.0 ml/min
DetectionUV 280 nm

Class of CompoundsEstrogen
Analyzing CompoundsEstrone, Estradiol, Estetrol, Estriol

Application Column

Chromni™

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 3 µm
Pore Size: 100 A
Column options: dual ended

Add to cart
Application Analytes:
Estetrol
Estradiol
Estriol
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.

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.

Select options

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.

Select options
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.