lenvatinib Impurity (Stage-1)
Synonyms: 1-(4-(5-(Benzyloxy)-2-nitrophenoxy)-2-chlorophenyl)-3-cyclopropylurea
lenvatinib Impurity (Stage-1) – Lenvatinib impurity standard. C23H20ClN3O5, MW 453.88. Request a quote: COA, bulk packs and worldwide export.
About lenvatinib Impurity (Stage-1)
lenvatinib Impurity (Stage-1) is an impurity of Lenvatinib from the Vaqora Chemicals catalogue. The compound has the formula C23H20ClN3O5, corresponding to a molecular weight of 453.88 g/mol.
The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.
As a characterised impurity of Lenvatinib, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. It is used across pharmaceutical manufacturing and academic and industrial research.
We offer lenvatinib Impurity (Stage-1) in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers worldwide. Stock is available for quick dispatch.
Typical applications
- Analytical method development
- Method validation (AMV)
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Lenvatinib.
Lenvatinib impuritiesSpecifications & identifiers
| Product name | lenvatinib Impurity (Stage-1) |
|---|---|
| Catalogue No. | VQ-005159 |
| Molecular formula | C23H20ClN3O5 |
| Molecular weight | 453.88 g/mol |
| Grade | Reference Standard |
| HSN code | 38229090 |
| Physical form | Solid |
|---|
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Frequently asked questions
What is the molecular formula and molecular weight of lenvatinib Impurity (Stage-1)?
lenvatinib Impurity (Stage-1) has the molecular formula C23H20ClN3O5 and a molecular weight of 453.88 g/mol.
What is lenvatinib Impurity (Stage-1) used for?
lenvatinib Impurity (Stage-1) is supplied as a characterised reference material related to Lenvatinib. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.
Which grade and pack sizes of lenvatinib Impurity (Stage-1) can I order?
We supply lenvatinib Impurity (Stage-1) in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg, 250 mg, 500 mg packs. Larger bulk quantities and custom packing are quoted on request.
Do you provide a COA and SDS with lenvatinib Impurity (Stage-1)?
Yes. Every lot of lenvatinib Impurity (Stage-1) is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.
Can lenvatinib Impurity (Stage-1) be shipped internationally?
Yes. We export lenvatinib Impurity (Stage-1) worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about lenvatinib Impurity (Stage-1)
We reply within one business day with price, pack options, lead time and documentation.