Vortioxetine Impurity 1 is a chemical impurity found in vortioxetine, a medication used for the treatment of major depressive disorder. This impurity, being a potential degradant, can affect the purity and therapeutic effectiveness of the drug. It is characterized by its ability to impact the quality of vortioxetine formulations, necessitating strict monitoring and control to ensure the medication's safety and efficacy.
1293489-71-0
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Basic information
- Product Name: Vortioxetine Impurity 1
- Synonyms: Vortioxetine Impurity 1;Vortioxetine Imp.A
- CAS NO:1293489-71-0
- Molecular Formula: C17H20N2S
- Molecular Weight: 284.4191
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1293489-71-0.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: Vortioxetine Impurity 1(CAS DataBase Reference)
- NIST Chemistry Reference: Vortioxetine Impurity 1(1293489-71-0)
- EPA Substance Registry System: Vortioxetine Impurity 1(1293489-71-0)
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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: 1293489-71-0(Hazardous Substances Data)
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1293489-71-0 Usage
Uses
Used in Pharmaceutical Quality Control:Vortioxetine Impurity 1 is used as a quality control parameter for ensuring the purity and effectiveness of vortioxetine. It is crucial for maintaining the safety and efficacy of the medication, as its presence can influence the drug's performance.
Used in Regulatory Compliance:
In the pharmaceutical industry, Vortioxetine Impurity 1 is used as a benchmark for compliance with regulatory guidelines that govern the acceptable levels of impurities in pharmaceutical products. Adhering to these guidelines is essential for upholding the quality and integrity of vortioxetine and other similar medications.
Used in Drug Stability Studies:
Vortioxetine Impurity 1 serves as an indicator in stability studies, which are conducted to understand how the drug behaves under various conditions. Monitoring the formation and levels of this impurity can provide insights into the stability and shelf life of vortioxetine products.
Used in Pharmaceutical Formulation Development:
During the development of pharmaceutical formulations, Vortioxetine Impurity 1 is considered to optimize the manufacturing process and final product quality. Controlling the levels of this impurity can help in formulating vortioxetine in a way that maximizes its therapeutic benefits while minimizing potential side effects due to impurities.
Check Digit Verification of cas no
The CAS Registry Mumber 1293489-71-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,3,4,8 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.Calculate Digit Verification of CAS Registry Number 1293489-71:
(9*1)+(8*2)+(7*9)+(6*3)+(5*4)+(4*8)+(3*9)+(2*7)+(1*1)=200
200 % 10 = 0
So 1293489-71-0 is a valid CAS Registry Number.
1293489-71-0Upstream product
1293489-71-0Downstream Products
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Vortioxetine Impurity 1
