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Sodium feredetate
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Looking for Sodium feredetate API 15708-41-5?
- Description:
- Here you will find a list of producers, manufacturers and distributors of Sodium feredetate. You can filter on certificates such as GMP, FDA, CEP, Written Confirmation and more. Send inquiries for free and get in direct contact with the supplier of your choice.
- API | Excipient name:
- Sodium feredetate
- Synonyms:
- Feredato de sodio , Ferédétate de sodium , Ferric sodium EDTA , Ferric sodium ethylenediaminetetraacetate , Ferrostrane , Ferrostrene , Monosodium ferric EDTA , Natrii feredetas , Sodium ferric EDTA , Sodium iron EDTA , Sodium ironedetate
- Cas Number:
- 15708-41-5
- DrugBank number:
- DB13381
- Unique Ingredient Identifier:
- 403J23EMFA
General Description:
Sodium feredetate is a chemical compound identified by the CAS number 15708-41-5. It is known for its distinct pharmacological properties and applications.
Classification:
Sodium feredetate belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups, classified under the direct parent group Tetracarboxylic acids and derivatives. This compound is a part of the Organic compounds, falling under the Organic acids and derivatives superclass, and categorized within the Carboxylic acids and derivatives class, specifically within the Tetracarboxylic acids and derivatives subclass.
Categories:
Sodium feredetate is categorized under the following therapeutic classes: Acetates, Acids, Acyclic, Amines, Antianemic Preparations, Blood and Blood Forming Organs, Compounds used in a research, industrial, or household setting, Diamines, Ethylenediamines, Iron Chelating Agents, Iron Compounds, Iron Preparations, Iron Trivalent, Oral Preparations, Parenteral Iron Replacement, Polyamines, Sequestering Agents. These classifications highlight the drug's diverse therapeutic applications and its importance in treating various conditions.
Sodium feredetate is a type of Other substances
The pharmaceutical industry encompasses a diverse range of active pharmaceutical ingredients (APIs) that are used in the production of various medications. One category of APIs is known as other substances. This category includes substances that do not fall under the conventional classifications such as antibiotics, analgesics, or antihypertensives.
Other substances in pharmaceutical APIs consist of a broad array of chemical compounds with unique properties and applications. These substances play a crucial role in the formulation and development of specialized medications, catering to specific therapeutic needs. The category encompasses various substances like excipients, solvents, stabilizers, and pH adjusters.
Excipients are inert substances that aid in the manufacturing process and enhance the stability, bioavailability, and patient acceptability of pharmaceutical formulations. Solvents are used to dissolve other ingredients and facilitate their incorporation into the final product. Stabilizers ensure the integrity and shelf life of medications by preventing degradation or chemical changes. pH adjusters help maintain the desired pH level of a formulation, which can influence the drug's efficacy and stability.
Pharmaceutical manufacturers carefully select and incorporate specific other substances into their formulations, adhering to regulatory guidelines and quality standards. These substances undergo rigorous testing and evaluation to ensure their safety, efficacy, and compatibility with the desired pharmaceutical product. By employing other substances in API formulations, pharmaceutical companies can optimize drug delivery, improve patient compliance, and enhance therapeutic outcomes.
In summary, the other substances category of pharmaceutical APIs comprises a diverse range of chemicals, including excipients, solvents, stabilizers, and pH adjusters. These substances contribute to the formulation, stability, and performance of medications, enabling pharmaceutical manufacturers to develop specialized products that meet specific therapeutic requirements.
