Cas no 423169-40-8 ([2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride)

[2-(Hydroxymethyl)-3-pyridyl]methanol hydrochloride is a versatile chemical intermediate with applications in pharmaceutical and organic synthesis. The compound features two hydroxymethyl groups attached to a pyridine ring, enhancing its reactivity as a building block for complex molecules. Its hydrochloride salt form improves stability and solubility, facilitating handling and storage. This derivative is particularly valuable in the synthesis of bioactive compounds, including potential drug candidates, due to its bifunctional reactivity and compatibility with diverse reaction conditions. The pyridine core also contributes to its utility in coordination chemistry and catalysis. High purity grades are available to meet rigorous research and industrial requirements.
[2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride structure
423169-40-8 structure
Product Name:[2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride
CAS No:423169-40-8
MF:C7H10ClNO2
MW:175.612801074982
MDL:MFCD08436996
CID:1026709
PubChem ID:17750570
Update Time:2025-11-02

[2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2,3-Pyridinedimethanol hydrochloride
    • [2-(hydroxymethyl)pyridin-3-yl]methanol,hydrochloride
    • 2,3-Dihydroxymethylpyridine hydrochloride
    • Pyridine-2,3-diyldimethanol hydrochloride
    • QC-3646
    • RW4094
    • [2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride
    • 423169-40-8
    • AMY3649
    • pyridine-2,3-diyldimethanol hcl
    • (2-hydroxymethyl-pyridin-3-yl)-methanol hydrogen chloride
    • A872905
    • s11918
    • AS-65068
    • MFCD08436996
    • bis(oxymethyl)pyridine hydrochloride
    • CS-0060369
    • AKOS015920294
    • pyridine-2,3-diyldimethanolhydrochloride
    • [2-(hydroxymethyl)pyridin-3-yl]methanol;hydrochloride
    • 2,3-Dihydroxymethylpyridine HCl
    • [3-(hydroxymethyl)pyridin-2-yl]methanol hydrochloride
    • F8880-3849
    • (Pyridine-2,3-diyl)dimethanol--hydrogen chloride (1/1)
    • 2,3-Bis(hydroxymethyl)pyridine hydrochloride
    • C7H10ClNO2
    • DTXSID00590577
    • EN300-127160
    • XHNKWLMBRMJUTQ-UHFFFAOYSA-N
    • [2-(HYDROXYMETHYL)PYRIDIN-3-YL]METHANOL HYDROCHLORIDE
    • SB54654
    • MDL: MFCD08436996
    • Inchi: 1S/C7H9NO2.ClH/c9-4-6-2-1-3-8-7(6)5-10;/h1-3,9-10H,4-5H2;1H
    • InChI Key: XHNKWLMBRMJUTQ-UHFFFAOYSA-N
    • SMILES: Cl.OCC1=CC=CN=C1CO

Computed Properties

  • Exact Mass: 175.04000
  • Monoisotopic Mass: 175.0400063g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 97.6
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 53.4?2

Experimental Properties

  • PSA: 53.35000
  • LogP: 0.86820

[2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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[2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride Production Method

Additional information on [2-(hydroxymethyl)-3-pyridyl]methanol;hydrochloride

Comprehensive Guide to [2-(hydroxymethyl)-3-pyridyl]methanol Hydrochloride (CAS 423169-40-8): Properties, Applications, and Market Insights

[2-(hydroxymethyl)-3-pyridyl]methanol hydrochloride (CAS 423169-40-8) is a specialized pyridine derivative with significant potential in pharmaceutical and chemical research. This compound, characterized by its dual hydroxylmethyl functional groups, has garnered attention for its unique chemical properties and versatile applications. In this detailed guide, we explore its molecular structure, synthesis methods, industrial uses, and emerging trends in research.

The chemical structure of [2-(hydroxymethyl)-3-pyridyl]methanol hydrochloride features a pyridine ring substituted with two hydroxymethyl groups at positions 2 and 3, with the hydrochloride salt enhancing its stability. This configuration makes it particularly valuable as a building block in organic synthesis, especially for creating complex molecules in drug development. Recent studies highlight its role as a precursor for biologically active compounds, aligning with current pharmaceutical industry demands for novel synthetic intermediates.

From a synthesis perspective, this compound is typically produced through controlled reduction reactions of corresponding pyridine carboxylic acid derivatives. The hydrochloride form (CAS 423169-40-8) offers improved solubility in polar solvents compared to its free base counterpart, making it preferable for many laboratory applications. Researchers particularly value its stability under various pH conditions, which is crucial for multi-step synthetic processes in medicinal chemistry.

In pharmaceutical applications, [2-(hydroxymethyl)-3-pyridyl]methanol hydrochloride serves as a key intermediate for developing central nervous system (CNS) drugs and enzyme inhibitors. Its structural similarity to nicotinamide derivatives makes it relevant for research in metabolic disorders, coinciding with growing interest in diabetes and obesity-related therapeutics. The compound's ability to form stable complexes also contributes to its use in catalysis research and material science applications.

The global market for pyridine derivatives like CAS 423169-40-8 has shown steady growth, driven by increasing pharmaceutical R&D investments. Current market analysis indicates rising demand in Asia-Pacific regions, particularly for high-purity chemical intermediates. Environmental considerations have also prompted development of greener synthesis methods for such compounds, reflecting broader industry sustainability trends.

Quality control for [2-(hydroxymethyl)-3-pyridyl]methanol hydrochloride typically involves HPLC analysis and spectroscopic characterization (NMR, MS). Storage recommendations include protection from moisture at controlled room temperature, with standard shelf lives of 24-36 months when properly packaged. These handling protocols ensure consistent performance in research applications while maintaining safety standards.

Emerging research directions for this compound include exploration in metal-organic frameworks (MOFs) and as a ligand in coordination chemistry. Its structural features make it promising for designing new functional materials, particularly in energy storage applications. Such developments position CAS 423169-40-8 as a compound with expanding scientific relevance beyond its traditional uses.

For researchers sourcing this material, current market availability shows consistent supply from specialty chemical manufacturers, with purity grades ranging from 95% to 99%. Pricing trends reflect typical fluctuations for research-grade chemicals, with bulk quantities offering cost advantages for industrial-scale applications. Proper documentation including certificates of analysis is essential when procuring this compound for regulated research environments.

Future prospects for [2-(hydroxymethyl)-3-pyridyl]methanol hydrochloride appear promising, particularly in targeted drug delivery systems and bioconjugation chemistry. Its molecular architecture allows for various modifications, making it adaptable to evolving pharmaceutical design strategies. As synthetic methodologies advance, this compound will likely find expanded applications in cutting-edge therapeutic development.

In summary, CAS 423169-40-8 represents a versatile chemical building block with growing importance across multiple scientific disciplines. Its balanced properties of reactivity and stability, combined with pharmaceutical relevance, ensure its continued use in both academic and industrial research settings. The compound's development trajectory mirrors broader trends in specialty chemicals innovation, particularly in life sciences applications.

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