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VAQORAErlotinib Impurity D(Stage-01)
Synonyms: 7-methoxy-6-(2-methoxyethoxy)-3-(2-methoxyethyl)quinazolin-4(3H)-one · Erlotinib Impurity D( Stage-01)
CAS No.—
FormulaC15H20N2O5
Mol. weight308.33
Catalogue No.VQ-004920
PurityReference Standard
HSN38229090
Erlotinib Impurity D(Stage-01) – Erlotinib impurity standard. C15H20N2O5, MW 308.33. Supplied by Vaqora Chemicals with COA, exported worldwide.
Pack sizesPrice on quotation · bulk available
10 mg
25 mg
50 mg
100 mg
Bulk / custom pack · kg to MT
Enquire Batch COA with every lot
16-section GHS SDS
Export to 120+ countries
DG-compliant packing
About Erlotinib Impurity D(Stage-01)
Erlotinib Impurity D(Stage-01) is an impurity of Erlotinib from the Vaqora Chemicals catalogue. Formula C15H20N2O5, molecular weight 308.33 g/mol. Alternative names: Erlotinib Impurity D( Stage-01).
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. Good laboratory practice and suitable PPE are recommended during handling.
As a characterised impurity of Erlotinib, 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.
Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Erlotinib Impurity D(Stage-01) is dispatched with a Certificate of Analysis (COA) to destinations worldwide. Stock is available for quick dispatch.
Typical applications
- Analytical method development
- Method validation (AMV)
- QC release testing
- ANDA / DMF filings
Industries
Related to Erlotinib
View every impurity, metabolite and intermediate we list for Erlotinib.
Erlotinib impuritiesSpecifications & identifiers
| Product name | Erlotinib Impurity D(Stage-01) |
|---|---|
| Catalogue No. | VQ-004920 |
| Molecular formula | C15H20N2O5 |
| Molecular weight | 308.33 g/mol |
| Grade | Reference Standard |
| HSN code | 38229090 |
| Physical form | Solid |
|---|
Documents
Frequently asked questions
What is the molecular formula and molecular weight of Erlotinib Impurity D(Stage-01)?
Erlotinib Impurity D(Stage-01) has the molecular formula C15H20N2O5 and a molecular weight of 308.33 g/mol.
What is Erlotinib Impurity D(Stage-01) used for?
Erlotinib Impurity D(Stage-01) is supplied as a characterised reference material related to Erlotinib. 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 Erlotinib Impurity D(Stage-01) can I order?
We supply Erlotinib Impurity D(Stage-01) in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.
Do you provide a COA and SDS with Erlotinib Impurity D(Stage-01)?
Yes. Every lot of Erlotinib Impurity D(Stage-01) 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 Erlotinib Impurity D(Stage-01) be shipped internationally?
Yes. We export Erlotinib Impurity D(Stage-01) worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Erlotinib Impurity D(Stage-01)
We reply within one business day with price, pack options, lead time and documentation.
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