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.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 70280-55-6
5-Bromo-2-(trifluoromethyl)aniline
pharmaceutical intermediate
Potassium N-(acetoacetyl)sulfanilate
pharmaceutical intermediate
4-Hydroxymethylthiazole
pharmaceutical intermediate
Ethyl 2-(5,6-dichloro-2-imino-1,2-dihydroquinazolin-3(4H )-yl)acetate hydrobromide
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(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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