Posaconazole CAS No.:171228-49-2

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Category:Active Pharmaceutical Ingredients   Own Brand:MT  /MOQ:100KG  /From China/  B2B only.

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Introduction

Chemical Name: Posaconazole

CAS No.: 171228-49-2

Assay: ≥99.0%

Appearance: White to off white powder

Posaconazole More Details:

Specification:

Appearance White to off white powder

Purity 99.0% Min

Melting point 170-172 °C(lit.)

Boiling point 850.7±75.0 °C

Density 1.36±0.1 g

Flashing point 9℃

Posaconazole Usage:

For patients with invasive aspergillosis refractory to amphotericin B or itraconazole or patients who cannot tolerate these medications.Posaconazole

Packaging and Shipping:

25KG/drum

Posaconazole Storage:

Stored in a dry and ventilated warehouse; keep away from sunshine; avoid fire; avoid moisture.

Item
Details
Name & CAS
Posaconazole (CAS No.: 171228 – 49 – 2). Its chemical name is (2S,3R,4S,5R)-5-(4 – fluorophenyl)-2-[(1R,2R)-2 – (2,4 – difluorophenyl)-2 – hydroxy – 1 – methyl – ethyl]-4 – (1H – 1,2,4 – triazol – 1 – yl)tetrahydro – 3 – furyl]methyl] – 1,3 – oxazole. The molecular formula is \(C_{37}H_{32}F_3N_5O_4\), and it has a molecular weight of 691.68 g/mol. It is a white to off – white crystalline powder.
Properties
Solubility: Practically insoluble in water, soluble in dimethyl sulfoxide, and sparingly soluble in ethanol. It is stable under normal storage conditions but may degrade when exposed to high temperatures, strong acids, or alkalis. It has a relatively long shelf – life when stored properly, protected from light and moisture.
Pharmacology
Posaconazole is a broad – spectrum antifungal agent. It works by inhibiting the enzyme lanosterol 14α – demethylase, which is involved in the synthesis of ergosterol, a key component of the fungal cell membrane. By blocking ergosterol synthesis, it disrupts the integrity and function of the fungal cell membrane, leading to the death of the fungus. It is effective against a wide range of fungal species, including Aspergillus, Candida, and some rare and emerging fungal pathogens. It is used for the prophylaxis and treatment of invasive fungal infections in immunocompromised patients, such as those with hematological malignancies, undergoing stem cell transplantation, or with acquired immunodeficiency syndrome (AIDS).
Side Effects
Common side effects include gastrointestinal symptoms such as nausea, vomiting, diarrhea, and abdominal pain. Headache, dizziness, and fatigue may also occur. In some cases, it can cause elevated liver enzymes, indicating potential liver function impairment. Rarely, serious allergic reactions, including anaphylaxis, may happen. There is also a risk of QT – interval prolongation, which can potentially lead to cardiac arrhythmias, especially in patients with pre – existing cardiac conditions or those taking other medications that can affect the QT interval.
Usage
It is available in oral suspension, delayed – release tablets, and intravenous injection forms. For prophylaxis of invasive fungal infections in high – risk patients, the oral suspension is often given at a dose of 200 mg three times a day. For the treatment of established fungal infections, the dosage may vary depending on the type and severity of the infection, but can range from 300 mg once or twice a day. The intravenous form is typically used when oral administration is not possible, with a loading dose followed by a maintenance dose. Treatment duration can range from several weeks to months, depending on the patient’s response and the nature of the infection.
Storage
Store in a tightly closed container, protected from light, and in a cool place (preferably between 15 – 30 °C). For the oral suspension, once opened, it should be stored in the refrigerator and used within a specified time frame, usually 14 days. The tablets and injectable formulations should be stored according to the manufacturer’s instructions to maintain their stability and potency.

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