API's
Active Pharmaceutical Ingredients
Active Pharmaceutical Ingredients
Active Pharmaceutical Ingredient (API)
USP / BP / EP (as applicable)
Etoposide
C₂₉H₃₂O₁₃
588.56 g/mol
33419-42-0
(5S,5aR,8aR,9R)-5-(4,6-O-ethylidene-β-D-glucopyranosyloxy)-9-(4-hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3’,4’:6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one
Podophyllotoxin derivative
Antineoplastic agent
| Appearance | White to off-white crystalline powder |
|---|---|
| Solubility | Slightly soluble in water, freely soluble in DMSO and methanol |
| Melting Point | 236–252°C |
| pH | 5.0–7.0 |
Etoposide is a widely used chemotherapy medication derived from the American mandrake plant, used to treat various cancers. It belongs to the class of drugs known as topoisomerase II inhibitors and works by damaging DNA to kill rapidly dividing cancer cells.
Etoposide's primary mechanism of action (MOA) is to act as a topoisomerase II inhibitor, which leads to DNA damage and ultimately programmed cell death (apoptosis) in rapidly dividing cancer cells.
| 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 |
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.
We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.
7 to 21 business days from dispatch, depending on your location.
Etoposide is an anticancer drug used to treat lung cancer, testicular cancer, lymphomas, and leukemia by preventing cancer cells from dividing and growing.
Store at 2–8°C, protected from light and moisture, to maintain stability and potency during storage and transportation.
Etoposide API is packed in double polyethylene bags inside HDPE or fiber drums and shipped using validated cold-chain logistics, ensuring the product remains stable during international transport.
Manufactured under cGMP conditions, each batch undergoes testing for impurities, residual solvents, and microbial limits, and is released with a Certificate of Analysis (CoA).
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