Cas no 14341-48-1 (Bromoacetic Acid-d3)

Bromoacetic Acid-d3 (C?D?BrO?) is a deuterated analog of bromoacetic acid, where three hydrogen atoms are replaced by deuterium. This isotopically labeled compound is particularly valuable in NMR spectroscopy and mass spectrometry studies, offering enhanced signal resolution and reduced interference in structural and mechanistic investigations. Its high isotopic purity ensures reliable results in kinetic and metabolic research, where tracing molecular pathways is critical. Bromoacetic Acid-d3 is also used in organic synthesis as a stable labeled reagent, facilitating precise tracking of reaction intermediates. The compound’s consistent quality and stability make it a preferred choice for analytical and synthetic applications in pharmaceutical and chemical research.
Bromoacetic Acid-d3 structure
Bromoacetic Acid-d3 structure
Product Name:Bromoacetic Acid-d3
CAS No:14341-48-1
MF:C2H3BrO2
MW:141.966505289078
CID:120338
PubChem ID:24872380
Update Time:2025-08-05

Bromoacetic Acid-d3 Chemical and Physical Properties

Names and Identifiers

    • Acetic-d2 acid-d,bromo- (8CI,9CI)
    • < D(3)> -Bromessigsaeure
    • 2-bromo-2,2,O-trideuterio-acetic acid
    • 488224_ALDRICH
    • Brom-dideutero-methan-< 2H> -carbonsaeure
    • Bromessigsaeure-d(3)
    • Bromessigsaeure-d3
    • bromoacetic acid-d3
    • Bromtrideuterioessigsaeure
    • I04-9924
    • BROMOACETIC-D2 ACID-D
    • BROMOACETIC-D2 ACID-D, 98 ATOM % D
    • D98850
    • 14341-48-1
    • AKOS015894229
    • SCHEMBL1331191
    • deuterio 2-bromo-2,2-dideuterioacetate
    • Bromoacetic acid-d3, 98 atom % D
    • J-007810
    • DTXSID40481470
    • deuterio 2-bromo-2,2-dideuterio-acetate
    • Bromoacetic Acid-d3
    • MDL: MFCD00190384
    • Inchi: 1S/C2H3BrO2/c3-1-2(4)5/h1H2,(H,4,5)/i1D2/hD
    • InChI Key: KDPAWGWELVVRCH-RIAYTAFFSA-N
    • SMILES: BrC([2H])([2H])C(=O)O[2H]

Computed Properties

  • Exact Mass: 140.95047g/mol
  • Monoisotopic Mass: 140.95047g/mol
  • Isotope Atom Count: 3
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 5
  • Rotatable Bond Count: 1
  • Complexity: 42.9
  • 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
  • Topological Polar Surface Area: 37.3?2

Experimental Properties

  • Color/Form: Not available
  • Melting Point: 47-49?°C (lit.)
  • Boiling Point: 208?°C(lit.)
  • Flash Point: >230?°F
  • Solubility: Not available

Bromoacetic Acid-d3 Security Information

Bromoacetic Acid-d3 Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
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Additional information on Bromoacetic Acid-d3

Bromoacetic Acid-d3: A Comprehensive Overview

Bromoacetic acid-d3, also known as Bromoacetic Acid-d3 with CAS No. 14341-48-1, is a chemical compound that has garnered significant attention in various scientific and industrial applications. This compound is a derivative of bromoacetic acid, where three of the hydrogen atoms in the methyl group have been replaced with deuterium atoms. The introduction of deuterium into the structure imparts unique properties, making it valuable in fields such as analytical chemistry, pharmacology, and materials science.

Recent advancements in isotopic labeling techniques have highlighted the importance of Bromoacetic Acid-d3 in studying metabolic pathways and enzyme mechanisms. Researchers have utilized this compound to track biochemical transformations with high precision, leveraging the distinct mass spectrometry signatures provided by deuterium. For instance, a 2022 study published in *Analytical Chemistry* demonstrated how Bromoacetic Acid-d3 can serve as a stable isotope standard for quantifying metabolites in complex biological systems.

The synthesis of Bromoacetic Acid-d3 involves a multi-step process that begins with the bromination of acetic acid, followed by selective deuteration. This process requires precise control over reaction conditions to ensure high isotopic purity. A 2023 paper in *Journal of Organic Chemistry* detailed an optimized synthesis route that employs palladium-catalyzed cross-coupling reactions, significantly improving yield and purity.

In terms of applications, Bromoacetic Acid-d3 has found utility in drug discovery and development. Its use as an intermediate in medicinal chemistry has enabled the creation of novel therapeutic agents with enhanced pharmacokinetic profiles. For example, a 2021 study in *Medicinal Chemistry Communications* reported the successful incorporation of Bromoacetic Acid-d3 into lead compounds targeting cancer cells, demonstrating improved bioavailability and reduced toxicity.

Moreover, Bromoacetic Acid-d3 plays a pivotal role in materials science, particularly in the development of advanced polymers and coatings. Its ability to undergo controlled polymerization under specific conditions has led to the creation of high-performance materials with tailored properties. A 2022 article in *Macromolecules* explored its application in synthesizing deuterated polymers for use in neutron scattering studies, providing deeper insights into polymer dynamics.

From an environmental perspective, understanding the fate and transport of Bromoacetic Acid-d3 in natural systems is crucial for risk assessment and regulatory purposes. Recent studies have focused on its biodegradation pathways and potential impact on aquatic ecosystems. A 2023 report in *Environmental Science & Technology* highlighted that while Bromoacetic Acid-d3 exhibits similar environmental behavior to its non-deuterated counterpart, its isotopic signature allows for precise tracking in contaminated sites.

In conclusion, Bromoacetic Acid-d3 (CAS No. 14341-48-1) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique properties derived from deuterium incorporation make it an invaluable tool for researchers and industry professionals alike. As scientific advancements continue to unfold, the potential uses of this compound are expected to expand further, solidifying its role as a key player in modern chemistry.

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