Estriol Impurity 14 structure

Estriol Impurity 14

TL;DR: Estriol Impurity 14 (CAS 73088-23-0) is a chemical compound with molecular formula C18H22O5S and molecular weight 350.12 g/mol, supplied by Kehong Biological (Henan Kehong Biological Technology Co., Ltd.) with CRO/CDMO custom synthesis services.

[(9S,13S,14S,17R)-17-hydroxy-13-methyl-6,9,11,12,14,15,16,17-octahydrocyclopenta[a]phenanthren-3-yl] hydrogen sulfate

Also Known As: Estriol Impurity 14, 17-Dihydroequilin 3-sulfate, J2.201.335A, Estra-1,3,5(10),7-tetraene-3,17alpha-diol 3-sulfate, Sulfuric acid 17alpha-hydroxyestra-1,3,5(10),7-tetraene-3-yl ester

CAS: 73088-23-0
Molecular Formula C18H22O5S
Molecular Weight 350.12 g/mol
LogP 2.6
Topological Polar Surface Area 92.2 Ų
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 5
Rotatable Bonds 2
Exact Mass 350.1188
Heavy Atoms 24
Complexity 636.0

Chemical Identifiers

CAS Number 73088-23-0
SMILES C[C@]12CC[C@H]3C(=CCC4=C3C=CC(=C4)OS(=O)(=O)O)[C@@H]1CC[C@H]2O
InChIKey IVPYDRYLQPJSBW-SPUZQDLCSA-N

Patent-Derived Application Labels

Derived from 1 IPC patent classification(s) across the SureChEMBL global patent database.

Heterocyclic Building Blocks (1 patents)

Product Overview

Estriol Impurity 14 (CAS 73088-23-0), with molecular formula C18H22O5S and molecular weight 350.12 g/mol. IUPAC: [(9S,13S,14S,17R)-17-hydroxy-13-methyl-6,9,11,12,14,15,16,17-octahydrocyclopenta[a]phenanthren-3-yl] hydrogen sulfate.

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Safety Data Sheet (MSDS / SDS) View the Laboratory Chemical Safety Summary (LCSS) on PubChem — includes GHS classifications, hazard statements, first aid measures, and handling precautions.
View MSDS →

Chemical Property Profile of Estriol Impurity 14

XLogP
2.6
TPSA (Topological Polar Surface Area)
92.2
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
5
Rotatable Bonds
2
Heavy Atoms
24
Complexity
636.0
Exact Mass
350.1188
Monoisotopic Mass
350.1188
Data Source: Chemical property values are referenced from PubChem, the world's largest open chemistry database maintained by the National Center for Biotechnology Information (NCBI), U.S. National Library of Medicine.

Property Insights of Estriol Impurity 14

The XLogP value of 2.6 suggests moderate lipophilicity, balancing water solubility and membrane permeability for Estriol Impurity 14. The TPSA of 92.2 Ų falls within the moderate polarity range, balancing permeability and solubility for Estriol Impurity 14. Following Lipinski's Rule of Five, Estriol Impurity 14 has 2 hydrogen bond donor(s) and 5 hydrogen bond acceptor(s), all within the drug-like range, suggesting favorable oral bioavailability potential.

Frequently Asked Questions

What is the typical lead time for this product?
Lead time typically ranges from 3-7 business days for in-stock items. For larger quantities or custom orders, please contact us for specific lead times.
Can you provide samples for testing?
Yes, we offer sample quantities for quality testing. Please submit an inquiry with your requirements and we will arrange samples accordingly.
What documentation do you provide with the product?
We provide COA (Certificate of Analysis), MSDS (Material Safety Data Sheet), and technical data sheets with each shipment.
Do you ship internationally?
Yes, we ship to most countries worldwide. Shipping costs and delivery times vary by location. Please contact us for specific shipping information.

Frequently Asked Questions

What is the CAS number of Estriol Impurity 14?

The CAS number of Estriol Impurity 14 is 73088-23-0.

What is the molecular formula of Estriol Impurity 14?

The molecular formula of Estriol Impurity 14 is C18H22O5S.

What is the molecular weight of Estriol Impurity 14?

The molecular weight of Estriol Impurity 14 is 350.12 g/mol.

Where can I buy Estriol Impurity 14?

You can request a quote for Estriol Impurity 14 directly from KEHONG BIO. Contact us or email info@kehongbio.com for pricing and availability.

Does KEHONG BIO offer custom synthesis for Estriol Impurity 14?

Yes, KEHONG BIO provides custom synthesis services for Estriol Impurity 14 and related compounds. Contact us with your specific requirements including quantity, purity, and timeline.

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