Buserelin EP Impurity A
Synonyms: (Des-Gly10,D-His2,D-Ser(tBu)6,Pro-NHEt9)-LHRH Acetate
Buserelin EP Impurity A (CAS 1872434-99-5) – Buserelin impurity standard. C62H90N16O15, MW 1299.5. COA included. Worldwide shipping from Vaqora Chemicals.
About Buserelin EP Impurity A
Listed under CAS 1872434-99-5, Buserelin EP Impurity A is a pharmacopeial impurity of Buserelin available from Vaqora Chemicals. Formula C62H90N16O15, molecular weight 1299.5 g/mol.
It is supplied as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.
This Buserelin impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.
Vaqora Chemicals supplies Buserelin EP Impurity A in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports worldwide. A Safety Data Sheet (SDS) and technical specifications are available on request.
Typical applications
- Pharmacopeial method verification
- Impurity profiling
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Buserelin.
Buserelin impuritiesGrade guides
Specifications & identifiers
| Product name | Buserelin EP Impurity A |
|---|---|
| Catalogue No. | VQ-029559 |
| CAS Number | 1872434-99-5 |
| IUPAC name | acetic acid;(2S)-N-[(2R)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-5-(diaminomethylideneamino)-1-[(2S)-2-(ethylcarbamoyl)pyrrolidin-1-yl]-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-[(2-methylpropan-2-yl)oxy]-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide |
| Molecular formula | C62H90N16O15 |
| Molecular weight | 1299.5 g/mol |
| Exact mass | 1298.6772 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | PYMDEDHDQYLBRT-ZLBHQSITSA-N |
| SMILES | CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](COC(C)(C)C)NC(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC3=CNC4=CC=CC=C43)NC(=O)[C@@H](CC5=CN=CN5)NC(=O)[C@@H]6CCC(=O)N6.CC(=O)O |
| PubChem CID | 145707491 |
| Physical form | Solid |
|---|---|
| H-bond donors / acceptors | 16 / 17 |
| TPSA | 478 Ų |
Documents
Frequently asked questions
What is the CAS number of Buserelin EP Impurity A?
The CAS Registry Number of Buserelin EP Impurity A is 1872434-99-5. It is also known as (Des-Gly10,D-His2,D-Ser(tBu)6,Pro-NHEt9)-LHRH Acetate.
What is the molecular formula and molecular weight of Buserelin EP Impurity A?
Buserelin EP Impurity A has the molecular formula C62H90N16O15 and a molecular weight of 1299.5 g/mol.
What is Buserelin EP Impurity A used for?
Buserelin EP Impurity A is supplied as a characterised reference material related to Buserelin. 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 Buserelin EP Impurity A can I order?
We supply Buserelin EP Impurity A 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 Buserelin EP Impurity A?
Yes. Every lot of Buserelin EP Impurity A 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 Buserelin EP Impurity A be shipped internationally?
Yes. We export Buserelin EP Impurity A worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Buserelin EP Impurity A
We reply within one business day with price, pack options, lead time and documentation.
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