Idelalisib Enatiomeric Impurity
Idelalisib Enatiomeric Impurity (CAS 2184933-01-3) – Idelalisib impurity standard. C22H18FN7O, MW 415.43. Vaqora Chemicals: COA, global shipping.
About Idelalisib Enatiomeric Impurity
Listed under CAS 2184933-01-3, Idelalisib Enatiomeric Impurity is an impurity of Idelalisib available from Vaqora Chemicals. With the molecular formula C22H18FN7O, it has a molar mass of 415.43 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. Handle it with standard laboratory precautions and appropriate personal protective equipment.
As a characterised impurity of Idelalisib, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.
Vaqora Chemicals supplies Idelalisib Enatiomeric Impurity in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports worldwide.
Typical applications
- Analytical method development
- Method validation (AMV)
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Idelalisib.
Idelalisib impuritiesSpecifications & identifiers
| Product name | Idelalisib Enatiomeric Impurity |
|---|---|
| Catalogue No. | VQ-048636 |
| CAS Number | 2184933-01-3 |
| Molecular formula | C22H18FN7O |
| Molecular weight | 415.43 g/mol |
| Grade | Reference Standard |
| HSN code | 38229090 |
| Physical form | Solid |
|---|
Documents
Frequently asked questions
What is the CAS number of Idelalisib Enatiomeric Impurity?
The CAS Registry Number of Idelalisib Enatiomeric Impurity is 2184933-01-3.
What is the molecular formula and molecular weight of Idelalisib Enatiomeric Impurity?
Idelalisib Enatiomeric Impurity has the molecular formula C22H18FN7O and a molecular weight of 415.43 g/mol.
What is Idelalisib Enatiomeric Impurity used for?
Idelalisib Enatiomeric Impurity is supplied as a characterised reference material related to Idelalisib. 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 Idelalisib Enatiomeric Impurity can I order?
We supply Idelalisib Enatiomeric Impurity 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 Idelalisib Enatiomeric Impurity?
Yes. Every lot of Idelalisib Enatiomeric Impurity 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 Idelalisib Enatiomeric Impurity be shipped internationally?
Yes. We export Idelalisib Enatiomeric Impurity worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Idelalisib Enatiomeric Impurity
We reply within one business day with price, pack options, lead time and documentation.
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