Dabigatran impurity P is a chemical compound used as a reference standard in the quality control and analysis of the pharmaceutical intermediate dabigatran. It serves primarily as an impurity marker to ensure the purity and consistency of dabigatran active pharmaceutical ingredients during manufacturing.
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.
Sourcing Dabigatran impurity P?
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Dabigatran etexilate
pharmaceutical raw material
Pradaxa
pharmaceutical raw material
Dabigatran etexilate mesylate
pharmaceutical raw material
8-Fluoro-1,3,4,5-tetrahydro-6H-azepino[5,4,3-cd]indol-6-one
pharmaceutical intermediate
3,6-Dichloropyridazine
pharmaceutical intermediate
Malonic acid
pharmaceutical intermediate
Ethyl acetoacetate
pharmaceutical intermediate
Dabigatran
pharmaceutical raw material
3-[[2-[[4-(hexoxycarbonylcarbamoyl)anilino]methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic acid
GYSMJNALQPNLBO-UHFFFAOYSA-N
CCCCCCOC(=O)NC(=O)C1=CC=C(C=C1)NCC2=NC3=C(N2C)C=CC(=C3)C(=O)N(CCC(=O)O)C4=CC=CC=N4
Sourcing Dabigatran impurity P?
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