Ezetimibe 3-Fluoro Impurity is a chemical byproduct generated during the synthesis and production of the cholesterol-lowering medication Ezetimibe. This impurity may be present in trace amounts in the final drug product and is crucial to monitor and control to ensure the medication's safety, efficacy, and compliance with regulatory standards.
1700622-06-5
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Basic information
- Product Name: (3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one
- Synonyms: (3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one;3-Fluoro Ezetimibe;Ezetimibe impurity 7;Ezetimibe Impurity 31;Ezetimibe Impurity G;N-Des(4-Fluorophenyl)-N-(3-fluorophenyl) Ezetimibe
- CAS NO:1700622-06-5
- Molecular Formula: C24H21F2NO3
- Molecular Weight: 409.4252464
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1700622-06-5.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 652.9±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.334±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 9.72±0.30(Predicted)
- CAS DataBase Reference: (3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one(CAS DataBase Reference)
- NIST Chemistry Reference: (3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one(1700622-06-5)
- EPA Substance Registry System: (3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one(1700622-06-5)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1700622-06-5(Hazardous Substances Data)
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1700622-06-5 Usage
Uses
Used in Pharmaceutical Industry:Ezetimibe 3-Fluoro Impurity is used as a quality control parameter for ensuring the purity and safety of the final Ezetimibe drug product. It is monitored and controlled to prevent any adverse effects on the medication's stability, bioavailability, and overall quality.
Ezetimibe 3-Fluoro Impurity is used as a regulatory compliance indicator to ensure that the final drug product meets the required standards set by health authorities and regulatory bodies. This helps maintain consumer confidence in the safety and efficacy of the medication.
In the Research and Development sector:
Ezetimibe 3-Fluoro Impurity is used as a subject of study for understanding the synthesis process of Ezetimibe and identifying ways to minimize or eliminate its presence in the final product. This research can lead to the development of more efficient production methods and improved drug quality.
Ezetimibe 3-Fluoro Impurity is also used in the development of analytical methods and techniques for detecting and quantifying impurities in pharmaceuticals. This aids in the implementation of robust quality control measures and ensures the consistent production of high-quality medications.
Check Digit Verification of cas no
The CAS Registry Mumber 1700622-06-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,0,6,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.Calculate Digit Verification of CAS Registry Number 1700622-06:
(9*1)+(8*7)+(7*0)+(6*0)+(5*6)+(4*2)+(3*2)+(2*0)+(1*6)=115
115 % 10 = 5
So 1700622-06-5 is a valid CAS Registry Number.
1700622-06-5Upstream product
1700622-06-5Downstream Products
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(3R,4S)-1-(3-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-one
