Perflenapent API Manufacturers

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Looking for Perflenapent API 678-26-2?

Description:
Here you will find a list of producers, manufacturers and distributors of Perflenapent. 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:
Perflenapent 
Synonyms:
Dodecafluoropentane , dodecafluoropentane emulsion (DDFPe) , Perfluoropentane  
Cas Number:
678-26-2 
DrugBank number:
DB11625 
Unique Ingredient Identifier:
483AU1Y5CZ

General Description:

Perflenapent, identified by CAS number 678-26-2, is a notable compound with significant therapeutic applications. Dodecafluoropentane is an ingredient in the EMA-withdrawn product EchoGen.

Classification:

Perflenapent belongs to the class of organic compounds known as organofluorides. These are compounds containing a chemical bond between a carbon atom and a fluorine atom, classified under the direct parent group Organofluorides. This compound is a part of the Organic compounds, falling under the Organohalogen compounds superclass, and categorized within the Organofluorides class, specifically within the None subclass.

Categories:

Perflenapent is categorized under the following therapeutic classes: Compounds used in a research, industrial, or household setting, Contrast Media, Diagnostic Uses of Chemicals, Hydrocarbons, Fluorinated, Hydrocarbons, Halogenated, Ultrasound Contrast Media. These classifications highlight the drug's diverse therapeutic applications and its importance in treating various conditions.

Perflenapent is a type of Contrast Media


Contrast media, a prominent category in the pharmaceutical API sector, plays a crucial role in medical imaging procedures. These specialized substances enhance the visibility of internal body structures during diagnostic tests such as X-rays, CT scans, and MRIs. By optimizing the contrast between different tissues or organs, contrast media enable healthcare professionals to obtain clearer and more detailed images for accurate diagnosis and treatment planning.

Contrast media can be classified into two main types: iodinated and gadolinium-based. Iodinated contrast agents are commonly used in X-ray and CT examinations, while gadolinium-based agents are employed in MRI scans. Both types are designed to interact with specific imaging technologies and provide contrasting properties to the surrounding tissues.

These pharmaceutical APIs are meticulously developed and undergo rigorous testing to ensure safety and efficacy. They are administered intravenously, orally, or via other routes, depending on the imaging technique and medical requirements. Contrast media are carefully formulated to optimize patient comfort and minimize adverse reactions.

Healthcare providers must consider various factors when selecting contrast media, including the patient's medical history, potential allergies, and the specific imaging procedure. Moreover, ongoing research and technological advancements in contrast media aim to improve image quality, reduce side effects, and enhance patient outcomes.

In summary, contrast media are an essential component of modern medical imaging. Their purpose is to enhance image visibility, aid in accurate diagnosis, and contribute to effective treatment planning. Through continuous advancements and stringent quality control, contrast media continue to play a vital role in improving medical imaging techniques and patient care.