9-Amino-1,2,3,4-tetrahydroacridin-1-ol-d3 Maleate

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Reagent Code: #58865
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CAS Number 1219806-48-0

science Other reagents with same CAS 1219806-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.35 g/mol
Formula C₁₇H₁₅D₃N₂O₅
inventory_2 Storage & Handling
Storage -20˚C

description Product Description

Used primarily in research and development, this compound serves as a deuterated analog in pharmacokinetic and metabolic studies. Its incorporation of deuterium atoms allows for tracing and analysis of drug metabolism pathways, aiding in the understanding of how similar non-deuterated compounds behave in biological systems. It is particularly valuable in the development of new pharmaceuticals, where precise tracking of drug distribution and breakdown is crucial. Additionally, it can be utilized in the synthesis of labeled compounds for use in NMR spectroscopy, enhancing the resolution and accuracy of molecular structure analysis.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿156,800.00

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9-Amino-1,2,3,4-tetrahydroacridin-1-ol-d3 Maleate
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Used primarily in research and development, this compound serves as a deuterated analog in pharmacokinetic and metabolic studies. Its incorporation of deuterium atoms allows for tracing and analysis of drug metabolism pathways, aiding in the understanding of how similar non-deuterated compounds behave in biological systems. It is particularly valuable in the development of new pharmaceuticals, where precise tracking of drug distribution and breakdown is crucial. Additionally, it can be utilized in the sy

Used primarily in research and development, this compound serves as a deuterated analog in pharmacokinetic and metabolic studies. Its incorporation of deuterium atoms allows for tracing and analysis of drug metabolism pathways, aiding in the understanding of how similar non-deuterated compounds behave in biological systems. It is particularly valuable in the development of new pharmaceuticals, where precise tracking of drug distribution and breakdown is crucial. Additionally, it can be utilized in the synthesis of labeled compounds for use in NMR spectroscopy, enhancing the resolution and accuracy of molecular structure analysis.

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