Cas no 83434-88-2 (D-Erythrose-2-13C (As a solution in water))

D-Erythrose-2-13C (as a solution in water) is a stable isotope-labeled derivative of D-erythrose, where the carbon-2 position is enriched with the 13C isotope. This compound is widely utilized in metabolic pathway studies, particularly in tracing carbon flux through glycolysis, the pentose phosphate pathway, and related biochemical processes. The aqueous solution format ensures ease of handling and direct compatibility with biological systems. Its high isotopic purity (>99% 13C) and chemical stability make it a reliable tracer for NMR and mass spectrometry-based analyses. Researchers value this compound for its role in elucidating metabolic mechanisms in plants, microorganisms, and mammalian systems, providing precise data for kinetic and fluxomic studies. The water-based formulation minimizes solvent interference in sensitive biological assays.
D-Erythrose-2-13C (As a solution in water) structure
83434-88-2 structure
Product Name:D-Erythrose-2-13C (As a solution in water)
CAS No:83434-88-2
MF:C4H8O4
MW:121.096576690674
CID:988883
PubChem ID:4475714
Update Time:2025-11-01

D-Erythrose-2-13C (As a solution in water) Chemical and Physical Properties

Names and Identifiers

    • D-[2-13C]erythrose
    • D-Erythrose-2-13C (As a solution in water)
    • FMAORJIQYMIRHF-BSZSZNCASA-N
    • D-Erythrose-2-13C
    • Butanal-2-13C, 2,3,4-trihydroxy-, [R-(R*,R*)]-
    • CHEBI:132185
    • D-[2-13C]THREOSE
    • D-[4-13C]THREOSE
    • tetrahydro-2,3,4-furantriol
    • tetrahydrofuran-2,3,4-triol
    • SCHEMBL7526648
    • 478506-49-9
    • D-[1-13C]threose
    • 90913-08-9
    • oxolane-2,3,4-triol
    • 2,3,4-trihydroxytetrahydrofuran
    • 83434-88-2
    • Inchi: 1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m0/s1/i3+1
    • InChI Key: YTBSYETUWUMLBZ-XNJVPAERSA-N
    • SMILES: OC[C@@H](O)[13C@@H](O)C=O

Computed Properties

  • Exact Mass: 120.04225873g/mol
  • Monoisotopic Mass: 120.04225873g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 84.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 3
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -1.9
  • Topological Polar Surface Area: 69.9?2

Experimental Properties

  • Density: 1.4±0.1 g/cm3
  • Melting Point: NA
  • Boiling Point: Not available
  • Flash Point: Not available
  • Vapor Pressure: Not available

D-Erythrose-2-13C (As a solution in water) Pricemore >>

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Additional information on D-Erythrose-2-13C (As a solution in water)

Comprehensive Overview of D-Erythrose-2-13C (CAS No. 83434-88-2) as a Water Solution

In the realm of isotopic labeling and biochemical research, D-Erythrose-2-13C (CAS No. 83434-88-2) stands out as a critical tool for metabolic studies and tracer applications. This compound, provided as a solution in water, is a 13C-labeled derivative of D-Erythrose, a four-carbon sugar that plays a pivotal role in carbohydrate metabolism. Researchers and pharmaceutical developers increasingly rely on isotopically labeled compounds like D-Erythrose-2-13C to unravel complex biochemical pathways, making it a hot topic in modern scientific inquiries.

The growing demand for stable isotope-labeled compounds is driven by advancements in NMR spectroscopy, mass spectrometry, and metabolic flux analysis. D-Erythrose-2-13C is particularly valuable for tracing carbon flow in glycolysis and the pentose phosphate pathway, addressing key questions in cancer metabolism and diabetes research. Its water-soluble formulation ensures ease of use in in vitro and in vivo studies, aligning with the trend toward high-throughput screening and precision medicine.

From an SEO perspective, users frequently search for terms like "13C-labeled sugars," "D-Erythrose applications," and "metabolic tracer compounds." These queries reflect the compound's relevance in biomedical research and drug discovery. Additionally, the CAS No. 83434-88-2 serves as a unique identifier, often used by procurement specialists to ensure accurate sourcing. The integration of these keywords enhances the visibility of this content for professionals seeking specialized biochemical reagents.

Quality and purity are paramount when working with isotopically enriched compounds. D-Erythrose-2-13C is typically characterized by HPLC, NMR, and LC-MS to verify its isotopic enrichment and chemical stability. Such rigorous validation meets the standards of Good Laboratory Practice (GLP) and caters to the needs of academic institutions, pharmaceutical companies, and contract research organizations (CROs).

Emerging trends in synthetic biology and enzyme engineering further amplify the utility of D-Erythrose-2-13C. For instance, its role in optimizing biocatalytic pathways for sustainable chemical production resonates with the global push toward green chemistry. This aligns with frequent search terms like "sustainable biomaterials" and "carbon-13 in biomanufacturing," highlighting the compound's cross-disciplinary appeal.

In summary, D-Erythrose-2-13C (CAS No. 83434-88-2) is a versatile reagent bridging gaps between basic research and applied science. Its water-soluble format, coupled with high isotopic purity, positions it as a staple in laboratories focused on metabolomics, structural biology, and therapeutic development. By addressing both niche and broad search queries, this overview caters to the evolving needs of the scientific community while adhering to SEO best practices.

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