Cas no 1219804-74-6 (N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE)
N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE Chemical and Physical Properties
Names and Identifiers
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- N,N′-Bis(3-aminopropyl-d6)-1,3-propanediamine
- N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE
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- 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 |
|---|---|---|---|---|---|---|---|---|
| TRC | B405901-0.5mg |
N,N'-Bis(3-aminopropyl-d6)-1,3-propanediamine |
1219804-74-6 | 0.5mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B405901-1mg |
N,N'-Bis(3-aminopropyl-d6)-1,3-propanediamine |
1219804-74-6 | 1mg |
$ 81.00 | 2023-04-18 | ||
| TRC | B405901-5mg |
N,N'-Bis(3-aminopropyl-d6)-1,3-propanediamine |
1219804-74-6 | 5mg |
$ 224.00 | 2023-04-18 | ||
| TRC | B405901-.5mg |
N,N'-Bis(3-aminopropyl-d6)-1,3-propanediamine |
1219804-74-6 | .5mg |
$ 64.00 | 2023-04-18 | ||
| A2B Chem LLC | AE35134-50mg |
N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE |
1219804-74-6 | 50mg |
$992.00 | 2024-04-20 |
N,N'-BIS(3-AMINOPROPYL-D6)-1,3-PROPANEDIAMINE Related Literature
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Suji Lee,Min Su Han Chem. Commun., 2021,57, 9450-9453
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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Michael Kappl,Paul M. Young,Daniela Traini,Sanyog Jain RSC Adv., 2016,6, 25789-25798
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Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
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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