Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF

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Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF

Name: Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF
Brand: Beijing Bovita Biomed Co.,Ltd
Price: 600 USD
Availability: InStock

Price 600 USD ($)/ Kilograms

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MOQ : 1 Kilograms

Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF Specification

Loss on Drying
0.5

Ph Level
4.0

Heavy Metal (%)
10ppm

Shelf Life
3 years Months

Storage
Room Temperature

HS Code
293399

Smell
Sweet

Solubility
water

Taste
Sweet

Particle Size
50ppm

Chemical Name
Tenofovir alafenamide hemifumarate

CAS No
1392275-56-7

Type
Immune Function Agents

Grade
Medicine Grade

Usage
Use for Hepatitis C and Hepatitis B

Purity(%)
99

Appearance
white powder

Physical Form
Powder

Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF Trade Information

Minimum Order Quantity
1 Kilograms

FOB Port
BEIJING

Payment Terms
Cash Against Delivery (CAD), Cash Advance (CA), Cash in Advance (CID), Telegraphic Transfer (T/T), Western Union

Supply Ability
100 Kilograms Per Month

Delivery Time
7 Days

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
Aluminum foil bags or cardboard barrels

Main Export Market(s)
Asia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East

Certifications
ISO 9001

About Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF

API Tenofovir alafenamide hemifumarate

CAS1392275-56-7

Appearance: White powder

Water 0.5%

Single impurity 0.5%

Total impurities 1.5%

GMP factory produce API Tenofovir alafenamide hemifumarate CAS 1392275-56-7 high Quality cheapest price

Superior Purity and Quality

Our Tenofovir alafenamide hemifumarate is available in powder form and boasts a 99% purity level, making it a top choice for medical applications. Meticulous control over heavy metal content (10ppm) and low loss on drying further ensures its reliability for pharmaceutical formulations. The product's sweet odor and taste do not interfere with its solubility or efficacy.

Applications in Hepatitis Therapy

Recognized for its effectiveness as an immune function agent, TAF is widely used for managing Hepatitis B and C. Its stability, grade, and consistent particle size make it suitable for integration into diverse dosage forms, supporting healthcare providers in delivering optimized therapies.

Convenient Storage and Long Shelf Life

TAF maintains its integrity for up to three years and should be stored at room temperature. The easy-to-handle powder form ensures straightforward processing by manufacturers and safe storage by healthcare facilities or distributors.

FAQ's of Tenofovir alafenamide hemifumarate CAS 1392275-56-7 TAF:

Q: How is Tenofovir alafenamide hemifumarate typically used in medical applications?

A: Tenofovir alafenamide hemifumarate is primarily used as an active pharmaceutical ingredient in the treatment of Hepatitis B and C. It is incorporated into specific antiviral medications that help to manage these chronic viral infections.

Q: What are the benefits of using TAF with a 99% purity grade?

A: A 99% purity grade ensures that the product is highly refined, minimizing impurities and optimizing its effectiveness and safety for medical use. This high purity contributes to consistent therapeutic outcomes and minimizes the risk of unwanted side effects.

Q: When should TAF be stored at room temperature?

A: TAF should always be stored at room temperature, as specified in the product details, to maintain its stability and extend its shelf life up to three years. Avoid exposing it to extreme temperatures or moisture, which could compromise its quality.

Q: Where is your Tenofovir alafenamide hemifumarate produced and exported from?

A: Our Tenofovir alafenamide hemifumarate is manufactured and exported from China by leading pharmaceutical suppliers and wholesalers, ensuring adherence to international standards.

Q: What is the process for ensuring consistent powder particle size and quality?

A: Our manufacturing process involves stringent quality controls to achieve a consistent particle size (50ppm) and meet the parameters for medicine-grade standards. Regular quality checks ensure compliance with loss on drying and heavy metal content limits.

Q: What makes this product suitable for pharmaceutical manufacturing?

A: TAF's high purity, low moisture content, water solubility, and stable white powder form make it ideal for pharmaceutical formulations, ensuring it can be efficiently processed into tablets or capsules without compromising effectiveness.

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