Cas no 1219804-74-6 (N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE)

N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE is a deuterated derivative of the polyamine N,N'-Bis(3-aminopropyl)-1,3-propanediamine, where six hydrogen atoms are replaced with deuterium. This isotopic labeling enhances its utility in mass spectrometry and NMR studies, improving signal resolution and reducing background interference. The compound is particularly valuable in metabolic research, pharmacokinetics, and mechanistic studies, where precise tracking of molecular pathways is required. Its high isotopic purity and stability make it suitable for use as an internal standard or tracer in analytical applications. The deuterium substitution also minimizes metabolic interference, ensuring reliable data in biological and chemical investigations.
N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE structure
1219804-74-6 structure
Product Name:N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE
CAS No:1219804-74-6
MF:C9H24N4
MW:188.313661575317
CID:1066103
Update Time:2025-10-05

N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE Chemical and Physical Properties

Names and Identifiers

    • N,N′-Bis(3-aminopropyl-d6)-1,3-propanediamine
    • N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE
    • Inchi: 1S/C9H24N4/c10-4-1-6-12-8-3-9-13-7-2-5-11/h12-13H,1-11H2
    • InChI Key: ZAXCZCOUDLENMH-UHFFFAOYSA-N
    • SMILES: C(CNC([H])([H])C([H])([H])C([H])([H])N)CNC([H])([H])C([H])([H])C([H])([H])N

N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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B405901-0.5mg
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Additional information on N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE

Research Brief on N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE (CAS: 1219804-74-6) and Its Applications in Chemical Biology and Pharmaceutical Research

The compound N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE (CAS: 1219804-74-6) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This deuterated polyamine derivative is increasingly being utilized as a critical reagent in drug discovery, metabolic studies, and proteomics research. Its unique structural properties, including the incorporation of deuterium atoms, make it particularly valuable for applications requiring isotopic labeling and mass spectrometry-based analysis.

Recent studies have highlighted the role of N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE in the development of novel therapeutic agents. For instance, researchers have employed this compound as a building block for synthesizing deuterated analogs of polyamine-based drugs, which are being investigated for their potential in treating cancer and neurodegenerative diseases. The deuterium substitution in the molecule enhances its metabolic stability, thereby improving the pharmacokinetic profiles of the resulting drug candidates.

In addition to its applications in drug development, this compound has been instrumental in advancing our understanding of polyamine metabolism. Polyamines, such as spermidine and spermine, play crucial roles in cell proliferation and differentiation. By using N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE as a labeled precursor, researchers have been able to trace the metabolic pathways of polyamines in various biological systems, providing insights into their regulatory mechanisms and potential therapeutic targets.

One of the most notable advancements involving this compound is its use in quantitative proteomics. The deuterium-labeled amine groups serve as stable isotopic tags, enabling precise quantification of proteins and peptides in complex biological samples. This approach has been particularly useful in biomarker discovery and the study of post-translational modifications, where accurate quantification is essential for identifying disease-related changes in protein expression.

Furthermore, recent publications have demonstrated the utility of N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE in the synthesis of advanced materials. For example, it has been used to create deuterated polymers with tailored properties for biomedical applications, such as drug delivery systems and tissue engineering scaffolds. The incorporation of deuterium into these materials can significantly alter their physical and chemical characteristics, offering new possibilities for innovation in material science.

Despite its promising applications, challenges remain in the large-scale synthesis and purification of N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE. Recent efforts have focused on optimizing synthetic routes to improve yield and purity, as well as developing more efficient methods for its incorporation into complex molecules. These advancements are expected to further expand the utility of this compound in both research and industrial settings.

In conclusion, N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE (CAS: 1219804-74-6) represents a versatile and valuable tool in chemical biology and pharmaceutical research. Its applications span drug discovery, metabolic studies, proteomics, and material science, highlighting its broad impact on the field. Ongoing research and technological developments are likely to uncover even more uses for this compound, solidifying its role as a key reagent in modern scientific investigations.

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