Phytonadione Impurities
General Information
Phytonadione Impurities and Phytonadione
Daicel Pharma is capable of offering Phytonadione impurity standards such as Phytonadione Impurity B, Phytonadione Impurity A, Phytonadione Diol Impurity, Phytonadione Diol Impurity-1 and more. The effectiveness, stability, and safety of Phytonadione is affected by impurities. Daicel Pharma can synthesize custom Phytonadione impurities according to global standards and regulations and worldwide delivery.
Phytonadione [CAS: 84-80-0] belongs to the class of phylloquinone. It functions as a cofactor, as a plant metabolite, and as a human metabolite. It is vitamin K and a phylloquinone member.
Phytonadione: Use and Commercial Availability
Oral phylloquinone treats prothrombin deficiency. It also treats hypoprothrombinemia. Parenteral phylloquinone (administered through intravenous, intramuscular, or subcutaneous routes) treats coagulation disorders caused by deficiencies in the production of coagulation factors II, VII, IX, and X due to vitamin K deficiency or any interference with vitamin K activity. This medicine is available under brand names such as Aquamephyton, Konakion, Mephyton, Vitamin K1, and Vitaped.
Phytonadione Structure and Mechanism of Action
The chemical name of Phytonadione is 2-Methyl-3-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecen-1-yl]-1,4-naphthalenedione. Its chemical formula is C31H46O2, and its molecular weight is approximately 450.7 g/mol.
Phytonadione is necessary for the formation of prothrombinogen and other blood clotting factors in the liver.
Phytonadione Impurities and Synthesis
Phytonadione impurities refer to unintended substances or contaminants present in Phytonadione1, a synthetic form of vitamin K. These impurities can impact the product’s effectiveness, stability, and safety.
Daicel Pharma provides a Certificate of Analysis (CoA) for various Phytonadione impurity standards, including Phytonadione Impurity B, Phytonadione Impurity A, Phytonadione Diol Impurity, Phytonadione Diol Impurity-1, and more. Our analytical facility, certified under cGMP, issues a comprehensive CoA and detailed characterization information such as 1H NMR, 13C NMR, IR, MASS, and HPLC purity2. Additional characterization details, like 13C-DEPT, can be provided upon request. Daicel Pharma is qualified to provide Phytonadione impurities and labeled compounds for assessing the effectiveness of generic Phytonadione. We offer highly pure Cis-Phytonadione-D7, Phytonadione-D7 (Mixture of Cis & Trans), and Tran-Phytonadione-D7, deuterium-labeled Phytonadione standard, essential for bioanalytical research and Bioavailability/Bioequivalence (BA/BE) studies.
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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