Phytonadione - Isotope Labelled Standards
References
FAQ's
References
- Isler, Otto; Doebel, Karl, Synthesis Of Vitamin K1 Using Boron Trifluoride Catalysts, Hoffmann-La Roche Inc., US2683176A, July 6, 1954
- Horn, George B., Determination of phytonadione in elemental diets by TLC-spectrophotodensitometry, Journal of Pharmaceutical Sciences, Volume: 67, Issue: 6, Pages: 834-6, 1978
Frequently Asked Questions
Can Phytonadione impurities be removed?
Complete removal of Phytonadione impurities is achievable through appropriate purification processes and quality control measures.
Are there regulatory guidelines for Phytonadione impurities?
Yes, there are regulatory guidelines in place for Phytonadione impurities.
What steps minimize Phytonadione impurities?
Pharmaceutical manufacturers take several measures to minimize impurities in Phytonadione. These include employing Good Manufacturing Practices (GMP), using high-quality raw materials, optimizing preparing processes, implementing proper storage and handling procedures, and conducting regular testing and monitoring to ensure product quality and purity.
What are the temperature conditions required to store Phytonadione impurities?
Phytonadione impurities are stored at a regulated room temperature of 2-8°C or as specified on the Certificate of Analysis (CoA).
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