Cas no 51209-49-5 (Cyclohexanone-d10)

Cyclohexanone-d10 is a deuterated analog of cyclohexanone, where all hydrogen atoms are replaced by deuterium (D). This compound is widely used as a solvent and internal standard in nuclear magnetic resonance (NMR) spectroscopy due to its high isotopic purity and minimal interference with proton signals. Its chemical stability and predictable behavior in reactions make it valuable for mechanistic studies and kinetic isotope effect investigations. Cyclohexanone-d10 is particularly useful in organic synthesis and analytical applications where precise deuteration is required. The compound’s consistent performance and compatibility with sensitive spectroscopic techniques underscore its importance in research and industrial laboratories.
Cyclohexanone-d10 structure
Cyclohexanone-d10 structure
Product Name:Cyclohexanone-d10
CAS No:51209-49-5
MF:C6D10O
MW:108.205
CID:380915
PubChem ID:12998629
Update Time:2025-05-24

Cyclohexanone-d10 Chemical and Physical Properties

Names and Identifiers

    • Cyclohexanone-2,2,3,3,4,4,5,5,6,6-d10
    • Cyclohexanone
    • CYCLOHEXANONE, [D10]
    • Cyclohexanone-d10
    • [2H10]cyclohexanone
    • Cyclohexanone-d10(9CI)
    • cyclohexanone-d11
    • d10-cyclohexanone
    • decadeuterio-cyclohexanone
    • perdeuteriocyclohexanone
    • Perdeuterocyclohexanone
    • Cyclohexanone-d10, 98 atom % D
    • JHIVVAPYMSGYDF-YXALHFAPSA-N
    • 2,2,3,3,4,4,5,5,6,6-Decadeuteriocyclohexan-1-one
    • 51209-49-5
    • CYCLOHEXANONE-D10-D
    • CYCLOHEXANONE-D10 (D, 98%)
    • (2H10)Cyclohexanone
    • EINECS 257-058-7
    • (~2~H_10_)Cyclohexanone
    • SCHEMBL753633
    • D99430
    • 2,2,3,3,4,4,5,5,6,6-decadeuteriocyclohexanone
    • DTXSID80965481
    • Inchi: InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2/i1D2,2D2,3D2,4D2,5D2
    • InChI Key: JHIVVAPYMSGYDF-YXALHFAPSA-N
    • SMILES: C1CCC(=O)CC1

Computed Properties

  • Exact Mass: 108.135932398g/mol
  • Monoisotopic Mass: 108.135932398g/mol
  • Isotope Atom Count: 10
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 0
  • Complexity: 68.2
  • 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: 2
  • XLogP3: nothing
  • Topological Polar Surface Area: 17.1?2

Experimental Properties

  • Color/Form: colorless liquid
  • Density: 1.044?g/mL?at 25?°C
  • Melting Point: -47?°C(lit.)
  • Boiling Point: 153?°C(lit.)
  • Flash Point: 116?°F
  • Refractive Index: n20/D 1.45(lit.)
  • PSA: 17.07000
  • LogP: 1.51960
  • Solubility: Not available
  • Vapor Pressure: No data available

Cyclohexanone-d10 Security Information

  • Signal Word:Warning
  • Hazard Statement: H226 (100%) H332 (100%)
  • Warning Statement: P264+P280+P305+P351+P338+P337+P313
  • Hazardous Material transportation number:UN 1915 3/PG 3
  • WGK Germany:2
  • Hazard Category Code: 10-20
  • Safety Instruction: 25
  • Hazardous Material Identification: Xn
  • Risk Phrases:10-20
  • Storage Condition:Store at 4 ° C, -4 ° C is better

Cyclohexanone-d10 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 Cyclohexanone-d10

Recent Advances in Chemical and Biomedical Research: Insights on 51209-49-5 and Cyclohexanone-d10

In the rapidly evolving field of chemical and biomedical research, the exploration of novel compounds and their applications continues to drive innovation. Among these, the compound with the CAS number 51209-49-5 and the deuterated solvent Cyclohexanone-d10 have garnered significant attention due to their unique properties and potential applications in pharmaceuticals, diagnostics, and material science. This research briefing aims to provide a comprehensive overview of the latest findings related to these substances, highlighting their roles in contemporary research and development.

The compound 51209-49-5, a relatively understudied molecule, has recently emerged as a candidate for various therapeutic applications. Recent studies have focused on its structural characteristics and interactions with biological targets, suggesting potential utility in drug design. Meanwhile, Cyclohexanone-d10, a deuterated analog of cyclohexanone, has been widely utilized as a solvent in nuclear magnetic resonance (NMR) spectroscopy due to its ability to provide sharp and well-resolved spectra. Its applications extend to pharmacokinetic studies and metabolic research, where deuterium labeling plays a crucial role in tracking molecular pathways.

One of the key advancements in the study of 51209-49-5 involves its potential as an inhibitor of specific enzymatic pathways. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that this compound exhibits selective binding to certain kinases, making it a promising candidate for targeted cancer therapies. The research employed advanced computational modeling and in vitro assays to validate these findings, paving the way for further preclinical investigations.

In parallel, Cyclohexanone-d10 has been instrumental in advancing metabolic research. A recent study in Analytical Chemistry highlighted its use in stable isotope labeling to monitor drug metabolism in vivo. The study reported enhanced sensitivity and accuracy in detecting metabolic intermediates, underscoring the solvent's value in pharmacokinetic profiling. Additionally, Cyclohexanone-d10 has found applications in polymer chemistry, where its deuterated properties facilitate the study of polymer dynamics and interactions.

Despite these promising developments, challenges remain in the widespread adoption of these compounds. For 51209-49-5, issues such as synthetic scalability and bioavailability need to be addressed to transition from laboratory research to clinical applications. Similarly, the high cost and limited availability of Cyclohexanone-d10 pose barriers to its broader use in research settings. However, ongoing efforts to optimize synthesis protocols and reduce production costs are expected to mitigate these challenges in the near future.

In conclusion, the latest research on 51209-49-5 and Cyclohexanone-d10 underscores their potential to contribute significantly to chemical and biomedical advancements. While further studies are needed to fully exploit their capabilities, the current findings provide a solid foundation for future exploration. Researchers and industry professionals are encouraged to consider these compounds in their work, leveraging their unique properties to drive innovation in drug development, diagnostics, and material science.

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