This compound is a deuterium-labeled pharmaceutical impurity reference standard, specifically a trideuteromethyl derivative of a chlorinated pyrimidine-dione structure. It is primarily used in analytical testing to identify and quantify related impurities in pharmaceutical 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.
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Alogliptin Impurity 07
pharmaceutical intermediate
11-?Chloro-?N-?methyl-?2-?phenyl-?3-?oxa-?4,?7-?diazatricyclo[6.4.0.?0{2,?4}?]?dodeca-?1(12)?,?6,?8,?10-?tetraen-?6-?amine
pharmaceutical raw material
Bupivacaine N-Oxide Hydrochloride Salt
pharmaceutical raw material
17a-Dutasteride
pharmaceutical raw material
(S)-Mirabegron
pharmaceutical raw material
2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]benzonitrile
pharmaceutical intermediate
2-((6-Chloro-3-ethyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)benzonitrile
pharmaceutical intermediate
2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-4-fluorobenzonitrile
pharmaceutical intermediate
2-[[6-chloro-2,4-dioxo-3-(trideuteriomethyl)pyrimidin-1-yl]methyl]benzonitrile
BVUJISIVAHYNLI-FIBGUPNXSA-N
[2H]C([2H])([2H])N1C(=O)C=C(N(C1=O)CC2=CC=CC=C2C#N)Cl
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