Cas no 16727-10-9 (N,N-Dimethylacetamide-d9)

N,N-Dimethylacetamide-d9 (DMA-d9) is a deuterated form of N,N-dimethylacetamide (DMA), where all nine hydrogen atoms are replaced with deuterium. This isotopically labeled compound is primarily used as a solvent in nuclear magnetic resonance (NMR) spectroscopy, offering enhanced signal resolution and reduced interference from protonated solvents. Its high isotopic purity (>98%) ensures reliable performance in analytical applications, particularly in structural elucidation and reaction monitoring. DMA-d9 is also valued for its chemical stability and compatibility with a wide range of organic and inorganic compounds. Its use is critical in deuterium labeling studies and mechanistic investigations where precise solvent effects must be minimized.
N,N-Dimethylacetamide-d9 structure
N,N-Dimethylacetamide-d9 structure
Product Name:N,N-Dimethylacetamide-d9
CAS No:16727-10-9
MF:C4H9NO
MW:96.1758162975311
CID:121846
Update Time:2025-05-23

N,N-Dimethylacetamide-d9 Chemical and Physical Properties

Names and Identifiers

    • Acetamide-2,2,2-d3,N,N-di(methyl-d3)-
    • N,N-DIMETHYLACETAMIDE-D9
    • Dimethylacet amide-d9
    • forNMRspectroscopy,deuterationdegree
    • N,N-Di[(2H3)methyl](2,2,2-2H3)acetamide
    • N,N-DIMETHYLACETAMIDE-D9 DEUTERATION DEG
    • N,N-Bis[(2H3)methyl](2,2,2-2H3)acetamide
    • N,N-Dimethylacetamide-D9 99.0 Atom % D
    • N,N-Dimethylacetamide-d9
    • Inchi: 1S/C4H9NO/c1-4(6)5(2)3/h1-3H3/i1D3,2D3,3D3
    • InChI Key: FXHOOIRPVKKKFG-GQALSZNTSA-N
    • SMILES: O=C(C([2H])([2H])[2H])N(C([2H])([2H])[2H])C([2H])([2H])[2H]

Computed Properties

  • Exact Mass: 105.18133
  • Isotope Atom Count: 9
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 6
  • Rotatable Bond Count: 1
  • Complexity: 58.6
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing

Experimental Properties

  • PSA: 20.31

N,N-Dimethylacetamide-d9 Pricemore >>

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Additional information on N,N-Dimethylacetamide-d9

N,N-Dimethylacetamide-d9: A Comprehensive Overview

N,N-Dimethylacetamide-d9, also known as DMA-d9, is a deuterated variant of N,N-Dimethylacetamide (DMA). This compound, with the CAS number 16727-10-9, has gained significant attention in various scientific fields due to its unique properties and applications. In this article, we will delve into the characteristics, synthesis, applications, and recent advancements related to N,N-Dimethylacetamide-d9.

The molecular structure of N,N-Dimethylacetamide-d9 consists of an acetamide group with two methyl groups attached to the nitrogen atom. The deuterium substitution in this compound makes it particularly useful in specialized applications. Recent studies have highlighted its role in deuterium labeling, which is crucial for various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy. The deuterium atoms in DMA-d9 provide distinct spectral signals, enabling precise structural elucidation and quantitative analysis in complex mixtures.

One of the most notable advancements in the synthesis of N,N-Dimethylacetamide-d9 involves the use of deuterated reagents and catalytic hydrogenation techniques. Researchers have optimized reaction conditions to achieve high yields and purity levels, ensuring its reliability for sensitive applications. The compound's ability to act as a solvent in deuterated environments has further expanded its utility in organic chemistry and materials science.

In the field of analytical chemistry, DMA-d9 has been employed as an internal standard for mass spectrometry (MS) analyses. Its stability and distinct isotopic signature make it ideal for quantifying trace amounts of compounds in complex matrices. Recent studies have demonstrated its effectiveness in metabolomics and proteomics research, where accurate quantification is paramount.

Beyond its analytical applications, N,N-Dimethylacetamide-d9 has found niche uses in pharmaceutical research. Its role as a co-solvent in drug delivery systems has been explored, with studies indicating improved solubility profiles for certain active pharmaceutical ingredients (APIs). The compound's compatibility with biological systems and its ability to enhance drug bioavailability are areas of ongoing investigation.

The environmental impact of using DMA-d9 has also been a topic of recent research. Studies suggest that its biodegradability and eco-friendly properties make it a sustainable choice for industrial applications. Efforts are underway to develop greener synthesis routes and recycling methods to minimize waste and energy consumption.

In conclusion, N,N-Dimethylacetamide-d9 stands out as a versatile compound with a wide range of applications across multiple disciplines. Its unique properties, combined with recent advancements in synthesis and application techniques, position it as an essential tool for researchers and industry professionals alike. As ongoing studies continue to uncover new potentials, the future of this compound looks promising.

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