Pioglitazone EP Impurity G
Synonyms: 3-[2-[(5-Ethyl-2-pyridinyl)ethoxy]phenyl] Pioglitazone Impurity · Pioglitazone Hydrochloride Impurity 31 · 3-[2-[(5-Ethyl-2-pyridinyl)ethoxy]phenyl]PioglitazoneImpurity
Pioglitazone EP Impurity G (CAS 952187-99-4) – Pioglitazone impurity standard. C34H35N3O4S, MW 581.7. From Vaqora Chemicals, with COA and worldwide delivery.
About Pioglitazone EP Impurity G
Listed under CAS 952187-99-4, Pioglitazone EP Impurity G is a pharmacopeial impurity of Pioglitazone available from Vaqora Chemicals. Formula C34H35N3O4S, molecular weight 581.7 g/mol. It is also known as Pioglitazone Hydrochloride Impurity 31.
It is supplied as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. Good laboratory practice and suitable PPE are recommended during handling.
Pharmaceutical QC and development laboratories use this impurity standard of Pioglitazone to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. It is used across pharmaceutical manufacturing and academic and industrial research.
Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Pioglitazone EP Impurity G is dispatched with a Certificate of Analysis (COA) to destinations worldwide.
Typical applications
- Pharmacopeial method verification
- Impurity profiling
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Pioglitazone.
Pioglitazone impuritiesGrade guides
Specifications & identifiers
| Product name | Pioglitazone EP Impurity G |
|---|---|
| Catalogue No. | VQ-033195 |
| CAS Number | 952187-99-4 |
| IUPAC name | 5-[[4-[2-(5-ethyl-2-pyridinyl)ethoxy]-3-[4-[2-(5-ethyl-2-pyridinyl)ethoxy]phenyl]phenyl]methyl]-1,3-thiazolidine-2,4-dione |
| Molecular formula | C34H35N3O4S |
| Molecular weight | 581.7 g/mol |
| Exact mass | 581.2348 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | VWPCWJMGWMWSGX-UHFFFAOYSA-N |
| SMILES | CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)C3=C(C=CC(=C3)CC4C(=O)NC(=O)S4)OCCC5=NC=C(C=C5)CC |
| PubChem CID | 17756322 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 7.1 |
| H-bond donors / acceptors | 1 / 7 |
| TPSA | 116 Ų |
Documents
Frequently asked questions
What is the CAS number of Pioglitazone EP Impurity G?
The CAS Registry Number of Pioglitazone EP Impurity G is 952187-99-4. It is also known as 3-[2-[(5-Ethyl-2-pyridinyl)ethoxy]phenyl] Pioglitazone Impurity, Pioglitazone Hydrochloride Impurity 31, 3-[2-[(5-Ethyl-2-pyridinyl)ethoxy]phenyl]PioglitazoneImpurity.
What is the molecular formula and molecular weight of Pioglitazone EP Impurity G?
Pioglitazone EP Impurity G has the molecular formula C34H35N3O4S and a molecular weight of 581.7 g/mol. Its IUPAC name is 5-[[4-[2-(5-ethyl-2-pyridinyl)ethoxy]-3-[4-[2-(5-ethyl-2-pyridinyl)ethoxy]phenyl]phenyl]methyl]-1,3-thiazolidine-2,4-dione.
What is Pioglitazone EP Impurity G used for?
Pioglitazone EP Impurity G is supplied as a characterised reference material related to Pioglitazone. 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 Pioglitazone EP Impurity G can I order?
We supply Pioglitazone EP Impurity G 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 Pioglitazone EP Impurity G?
Yes. Every lot of Pioglitazone EP Impurity G 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 Pioglitazone EP Impurity G be shipped internationally?
Yes. We export Pioglitazone EP Impurity G worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Pioglitazone EP Impurity G
We reply within one business day with price, pack options, lead time and documentation.
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