6-Ketoestradiol

97%

Reagent Code: #92853
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CAS Number 571-92-6

science Other reagents with same CAS 571-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.37 g/mol
Formula C₁₈H₂₂O₃
badge Registry Numbers
MDL Number MFCD00056457
thermostat Physical Properties
Melting Point 281-283 °C (lit.)
Boiling Point 478.9 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.249 g/cm3 at 25 °C (lit.)
Storage room temperature

description Product Description

6-Ketoestradiol is primarily utilized in research settings to study its effects on estrogen receptors and its potential role in hormone-related processes. It is often investigated for its interactions with estrogen metabolism and its impact on various physiological pathways, including those related to reproductive health. Researchers explore its potential applications in understanding hormone-dependent conditions and developing targeted therapies. Additionally, it may be used in biochemical assays to evaluate its binding affinity and activity in comparison to other estrogenic compounds. Its role in modulating cellular responses makes it a valuable compound in endocrinology and cancer research, particularly in studies focusing on estrogen receptor-positive cancers.

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Test Parameter Specification
Appearance White to Off-White to Pale Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿33,264.00
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6-Ketoestradiol
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6-Ketoestradiol is primarily utilized in research settings to study its effects on estrogen receptors and its potential role in hormone-related processes. It is often investigated for its interactions with estrogen metabolism and its impact on various physiological pathways, including those related to reproductive health. Researchers explore its potential applications in understanding hormone-dependent conditions and developing targeted therapies. Additionally, it may be used in biochemical assays to evaluate its binding affinity and activity in comparison to other estrogenic compounds. Its role in modulating cellular responses makes it a valuable compound in endocrinology and cancer research, particularly in studies focusing on estrogen receptor-positive cancers.
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