3-bromopyridine-2,4,5,6-d4

98%, 98 atom % D

Reagent Code: #147828
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CAS Number 66148-14-9

science Other reagents with same CAS 66148-14-9

blur_circular Chemical Specifications

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Weight 162.02 g/mol
Formula C₅D₄BrN
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a labeled internal standard in mass spectrometry and analytical chemistry for accurate quantification of pyridine derivatives in complex mixtures. Its deuterated structure allows clear differentiation from non-labeled compounds during detection, improving precision in pharmaceutical and environmental testing. Also serves as a building block in the synthesis of isotopically labeled drugs and bioactive molecules, where tracking metabolic pathways or reaction mechanisms is required. The bromine functionality enables selective cross-coupling reactions, facilitating incorporation into larger deuterated structures for research in drug metabolism and medicinal chemistry.

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inventory 5mg
10-20 days ฿3,040.00

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3-bromopyridine-2,4,5,6-d4
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Used as a labeled internal standard in mass spectrometry and analytical chemistry for accurate quantification of pyridine derivatives in complex mixtures. Its deuterated structure allows clear differentiation from non-labeled compounds during detection, improving precision in pharmaceutical and environmental testing. Also serves as a building block in the synthesis of isotopically labeled drugs and bioactive molecules, where tracking metabolic pathways or reaction mechanisms is required. The bromine func

Used as a labeled internal standard in mass spectrometry and analytical chemistry for accurate quantification of pyridine derivatives in complex mixtures. Its deuterated structure allows clear differentiation from non-labeled compounds during detection, improving precision in pharmaceutical and environmental testing. Also serves as a building block in the synthesis of isotopically labeled drugs and bioactive molecules, where tracking metabolic pathways or reaction mechanisms is required. The bromine functionality enables selective cross-coupling reactions, facilitating incorporation into larger deuterated structures for research in drug metabolism and medicinal chemistry.

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