Cas no 78832-54-9 (2-Naphthol-d7)

2-Naphthol-d7 is a deuterated derivative of 2-naphthol, where seven hydrogen atoms are replaced with deuterium. This isotopic labeling enhances its utility in nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry, providing improved signal resolution and reduced interference in analytical studies. The compound is particularly valuable in metabolic research, pharmacokinetics, and environmental tracing, where precise detection and quantification are critical. Its high isotopic purity and chemical stability ensure reliable performance in deuterium exchange reactions and mechanistic investigations. 2-Naphthol-d7 is synthesized under controlled conditions to meet stringent quality standards, making it a preferred choice for advanced research applications requiring isotopic labeling.
2-Naphthol-d7 structure
2-Naphthol-d7 structure
Product Name:2-Naphthol-d7
CAS No:78832-54-9
MF:C10H8O
MW:151.213054656982
CID:553527
PubChem ID:16213383
Update Time:2025-06-10

2-Naphthol-d7 Chemical and Physical Properties

Names and Identifiers

    • 2-Naphthalen-1,3,4,5,6,7,8-d7-ol
    • 2-NAPHTHOL-1,3,4,5,6,7,8-D7
    • 2-Naphthol-d7
    • (2H7)naphthalen-2-ol
    • 2-Naphthol-d71000μg
    • AKOS015912813
    • SCHEMBL13915068
    • HY-Y0110S1
    • D99463
    • DTXSID30583912
    • 2-Naphthol-1,3,4,5,6,7,8-d7, 97 atom % D
    • (~2~H_7_)Naphthalen-2-ol
    • (?H?)naphthalen-2-ol
    • CS-0564270
    • 1,3,4,5,6,7,8-heptadeuterionaphthalen-2-ol
    • 78832-54-9
    • 2-Naphthalen-1,3,4,5,6,7,8-d7-ol; 2-Naphthol-d7; 2-Naphthol (ring-D7)
    • DA-69814
    • Inchi: 1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H/i1D,2D,3D,4D,5D,6D,7D
    • InChI Key: JWAZRIHNYRIHIV-GSNKEKJESA-N
    • SMILES: OC1=C([2H])C([2H])=C2C([2H])=C([2H])C([2H])=C([2H])C2=C1[2H]

Computed Properties

  • Exact Mass: 151.101452096g/mol
  • Monoisotopic Mass: 151.101452096g/mol
  • Isotope Atom Count: 7
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • Complexity: 133
  • 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: 3
  • XLogP3: nothing
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • Density: 1.239
  • Melting Point: 120-122?°C(lit.)
  • Boiling Point: 285-286?°C(lit.)
  • Flash Point: 144°C
  • Refractive Index: 1.677

2-Naphthol-d7 Security Information

  • Hazardous Material transportation number:UN 3077 9 / PGIII
  • WGK Germany:3
  • Hazard Category Code: 22-36/37/38-50-20/22
  • Safety Instruction: 26-36-61-24/25
  • Hazardous Material Identification: Xn
  • Risk Phrases:22-36/37/38
  • Safety Term:26-36

2-Naphthol-d7 Pricemore >>

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Additional information on 2-Naphthol-d7

Professional Introduction to 2-Naphthol-d7 (CAS No. 78832-54-9)

2-Naphthol-d7, a deuterated derivative of 2-naphthol with the chemical formula C10H6D7O, is a specialized compound widely utilized in the field of chemical and pharmaceutical research. This isotope-labeled version of 2-naphthol is particularly valuable for its applications in analytical chemistry, drug metabolism studies, and as an internal standard in nuclear magnetic resonance (NMR) spectroscopy. The inclusion of deuterium atoms enhances the compound's stability and sensitivity, making it an indispensable tool for researchers seeking precise and reliable data.

The CAS number 78832-54-9 uniquely identifies this compound, ensuring consistency and accuracy in its classification and use. 2-Naphthol-d7 is derived from the parent compound 2-naphthol, a heterocyclic organic compound consisting of two fused benzene rings with a hydroxyl group (-OH) attached to one of the rings. The introduction of deuterium atoms (D) at specific positions in the molecular structure modifies its physical and chemical properties while maintaining its core structural integrity.

In recent years, the demand for isotope-labeled compounds like 2-Naphthol-d7 has surged due to advancements in metabolic studies and drug development. The use of deuterated compounds allows researchers to track metabolic pathways with greater precision, as deuterium atoms do not naturally occur in biological systems at significant levels. This distinction makes it easier to differentiate between labeled and endogenous compounds, thereby enhancing the resolution and accuracy of analytical techniques.

One of the most prominent applications of 2-Naphthol-d7 is in nuclear magnetic resonance (NMR) spectroscopy. NMR is a powerful analytical technique used to determine the molecular structure of compounds. The deuterated version improves the signal-to-noise ratio, enabling researchers to obtain clearer and more detailed spectra. This is particularly crucial when studying complex molecules such as pharmaceuticals, where precise structural information is essential for understanding their biological activity and interactions.

Recent studies have highlighted the utility of 2-Naphthol-d7 in drug metabolism research. By incorporating this labeled compound into drug formulations, researchers can monitor how drugs are metabolized within the body over time. This information is vital for optimizing drug dosages, predicting potential side effects, and developing new therapeutic agents. The ability to trace metabolic pathways with high fidelity has significantly accelerated the drug discovery process in recent years.

The chemical properties of 2-Naphthol-d7 make it an excellent candidate for various synthetic applications. Its aromatic structure allows for easy functionalization, enabling chemists to create derivatives with tailored properties for specific research or industrial purposes. Additionally, its stability under various conditions makes it suitable for long-term storage without degradation, ensuring consistent performance across multiple experiments.

In conclusion, 2-Naphthol-d7 (CAS No. 78832-54-9) represents a significant advancement in chemical research tools. Its unique properties enhance the capabilities of analytical techniques such as NMR spectroscopy and provide invaluable insights into drug metabolism and molecular structure determination. As research methodologies continue to evolve, compounds like 2-Naphthol-d7 will remain indispensable for scientists striving to push the boundaries of chemical and pharmaceutical innovation.

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