Plerixafor Impurity-9 (Stage-I)
Synonyms: 1,5,8,12-Tetraazabicyclo[10.2.2]hexadecane-13,14-dione
Plerixafor Impurity-9 (Stage-I) – Plerixafor impurity standard, 93.46%. C12H22N4O2, MW 254.33. COA included. Worldwide shipping from Vaqora Chemicals.
About Plerixafor Impurity-9 (Stage-I)
Plerixafor Impurity-9 (Stage-I) is an impurity of Plerixafor from the Vaqora Chemicals catalogue at a purity of 93.46%. The compound has the formula C12H22N4O2, corresponding to a molecular weight of 254.33 g/mol.
It is supplied 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.
As a characterised impurity of Plerixafor, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Our customers for this product work in pharmaceutical manufacturing and academic and industrial research.
Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Plerixafor Impurity-9 (Stage-I) 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
View every impurity, metabolite and intermediate we list for Plerixafor.
Plerixafor impuritiesSpecifications & identifiers
| Product name | Plerixafor Impurity-9 (Stage-I) |
|---|---|
| Catalogue No. | VQ-005565 |
| Molecular formula | C12H22N4O2 |
| Molecular weight | 254.33 g/mol |
| Grade | Reference Standard |
| Purity / assay | 93.46% |
| HSN code | 38229090 |
| Physical form | Solid |
|---|
Documents
Frequently asked questions
What is the molecular formula and molecular weight of Plerixafor Impurity-9 (Stage-I)?
Plerixafor Impurity-9 (Stage-I) has the molecular formula C12H22N4O2 and a molecular weight of 254.33 g/mol.
What is Plerixafor Impurity-9 (Stage-I) used for?
Plerixafor Impurity-9 (Stage-I) is supplied as a characterised reference material related to Plerixafor. 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 Plerixafor Impurity-9 (Stage-I) can I order?
We supply Plerixafor Impurity-9 (Stage-I) in Reference Standard (93.46%) 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 Plerixafor Impurity-9 (Stage-I)?
Yes. Every lot of Plerixafor Impurity-9 (Stage-I) 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 Plerixafor Impurity-9 (Stage-I) be shipped internationally?
Yes. We export Plerixafor Impurity-9 (Stage-I) worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Plerixafor Impurity-9 (Stage-I)
We reply within one business day with price, pack options, lead time and documentation.