Buserelin EP Impurity C is a peptide-related compound used as a reference standard for quality control in the manufacturing of the pharmaceutical intermediate buserelin. It serves as a characterized impurity to ensure the purity and consistency of buserelin batches during production.
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CAS 70280-55-6
2-AMINO-4-BROMOBENZOTRIFLUORIDE
Pharmaceutical intermediate and research compound
Potassium N-(acetoacetyl)sulfanilate
Pharmaceutical intermediate for sulfa drugs
(1,3-thiazol-4-yl)methanol
pharmaceutical intermediate
Ethyl 2-(2-amino-5,6-dichloro-4H-quinazolin-3-yl)acetate;hydrobromide
pharmaceutical intermediate
(2S)-1-[(2S)-2-[[(2S)-2-[[(2R)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]-3-hydroxypropanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-[(2-methylpropan-2-yl)oxy]propanoyl]amino]-4-methylpentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]-N-ethylpyrrolidine-2-carboxamide
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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)N