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Tenofovir Alafenamide Structure

PRODUCT TYPE

API

GRADE

USP / EP / BP

CHEMICAL FORMULA

C₂₀H₂₈N₆O₅P

IUPAC NAME

Isopropyl (2S)-2-[[[1R)-2-(6-amino-9H-purin-9-yl)-1-methoxypropan-2-yl] oxy] methyl-phenoxy phosphoryl] amino] propanoate

CAS NO

379270-37-8

MOLECULAR WEIGHT

476.5 g/mol

CHEMICAL CLASS

Nucleotide Reverse Transcriptase Inhibitor (NtRTI)

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White to off-white crystalline powder
Solubility Freely soluble in DMSO and methanol; slightly soluble in water
Melting Point 105–110°C (decomposes)
pH 4.5–6.5 (1% aqueous solution)

Product Description

Tenofovir Alafenamide is a novel nucleotide reverse transcriptase inhibitor used for the treatment of HIV-1 infection and chronic hepatitis B. It is a prodrug of tenofovir that delivers higher intracellular concentrations with lower systemic exposure, reducing the risk of renal and bone toxicity compared to Tenofovir Disoproxil Fumarate (TDF).

How Tenofovir Alafenamide Works

TAF is converted inside cells into tenofovir diphosphate. Compete with natural nucleotides to inhibit viral reverse transcriptase. Prevents viral DNA chain elongation, effectively reducing viral replication. Lower plasma tenofovir levels result in improved safety for kidneys and bones.

Use(s)

Adverse Effects

Why choose Salius for Tenofovir Alafenamide?

  1. GMP-Compliant Manufacturing Standards
    They maintain stringent WHO GMP standards, with some facilities FDA certified, and follows strict internal QC protocols. Every batch is tested in state-of-the-art labs before release, to ensure consistent quality, safety & efficacy.
  2. Cost-Effectiveness
    As an experienced generic API supplier and export house, Salius aims to deliver high-quality APIs at competitive prices—a key advantage for cost-sensitive and emerging markets.
  3. Global Export Experience & Documentation Support
    Salius regularly exports APIs, provides regulatory dossiers (DMF, impurity profiles), and supports filings for international clients—even in stringent regulated markets
  4. Documents We Provide
  5. Transparency & Trustworthiness
    They present as a government-recognized star export house with strong quality and delivery ratings.
Attribute Why Salius Pharma Is a Good Choice
Quality Certification WHO GMP, ISO 9001:2015, FDA audited facilities
Affordability & Generic Access Cost competitive generics for global supply
Export Experience Proven track record of supplying globally

What You Receive in Our Package

When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.

Each Shipment Includes:

Product

Expected Delivery Time

We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.

Overall Delivery Time:

7 to 21 business days from dispatch, depending on your location.

FAQs

It is used for HIV-1 infection and chronic hepatitis B treatment.

Cool, dry, ventilated area; protect from light and moisture.

Yes.

Salius Pharma exports globally, including regulated markets in the US, EU, and Asia.

Yes, stability and analytical data are provided with COA.

Contact Salius Pharma via email or phone with product name, quantity, and delivery details; a quotation and documentation package will be provided.

Place an Order or Request a Quote from Salius Pharma

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