Gefitinib Impurity-D (Stage-1)
Synonyms: 4-(3-((4-chloro-7-methoxy-3,4-dihydroquinazolin-6-yl)oxy)propyl)morpholine
Gefitinib Impurity-D (Stage-1) – Gefitinib impurity standard, 90.08%. C16H22ClN3O3, MW 339.82. Buy from Vaqora Chemicals with COA and worldwide shipping.
About Gefitinib Impurity-D (Stage-1)
Gefitinib Impurity-D (Stage-1) is an impurity of Gefitinib offered by Vaqora Chemicals at a purity of 90.08%. Formula C16H22ClN3O3, molecular weight 339.82 g/mol.
The product is provided as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Good laboratory practice and suitable PPE are recommended during handling.
This Gefitinib impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.
Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide. Stock is available for quick dispatch. A Safety Data Sheet (SDS) and technical specifications are available on request.
Typical applications
- Analytical method development
- Method validation (AMV)
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Gefitinib.
Gefitinib impuritiesSpecifications & identifiers
| Product name | Gefitinib Impurity-D (Stage-1) |
|---|---|
| Catalogue No. | VQ-005028 |
| Molecular formula | C16H22ClN3O3 |
| Molecular weight | 339.82 g/mol |
| Grade | Reference Standard |
| Purity / assay | 90.08% |
| HSN code | 38229090 |
| Physical form | Solid |
|---|
Documents
Frequently asked questions
What is the molecular formula and molecular weight of Gefitinib Impurity-D (Stage-1)?
Gefitinib Impurity-D (Stage-1) has the molecular formula C16H22ClN3O3 and a molecular weight of 339.82 g/mol.
What is Gefitinib Impurity-D (Stage-1) used for?
Gefitinib Impurity-D (Stage-1) is supplied as a characterised reference material related to Gefitinib. 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 Gefitinib Impurity-D (Stage-1) can I order?
We supply Gefitinib Impurity-D (Stage-1) in Reference Standard (90.08%) 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 Gefitinib Impurity-D (Stage-1)?
Yes. Every lot of Gefitinib Impurity-D (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 Gefitinib Impurity-D (Stage-1) be shipped internationally?
Yes. We export Gefitinib Impurity-D (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 Gefitinib Impurity-D (Stage-1)
We reply within one business day with price, pack options, lead time and documentation.