Molecular structure of 1-Naphthol, CAS Number: 90-15-3
1-Naphthol (CAS 90-15-3)
Alternate Names:
1-Hydroxynaphthalene
Application:
1-Naphthol is used in the manufacturing of dyes,
CAS Number:
90-15-3
Purity:
≥99%
Molecular Weight:
144.17
Molecular Formula:
C10H8O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
1-Naphthol, also referred to as 1-hydroxy-naphthalene, is an organic compound obtained from the aromatic hydrocarbon naphthalene. This compound exists as a white crystalline solid with a subtle odor and displays high solubility in organic solvents. Scientific research extensively employs 1-naphthol across multiple applications. It serves as a reagent in the synthesis of organic compounds, encompassing polymers, and dyes. Additionally, it acts as a catalyst in the polymerization process of vinyl monomers. Notably, 1-naphthol plays a vital role as a reactant in the synthesis of 1-naphthylacetic acid and its derivatives.
1-Naphthol (CAS 90-15-3) References
- Fluorescence properties of 1-naphthol, 2-naphthol and 1,2,3,4-tetrahydronaphthol in aqueous alcohol solvents with and without beta-cyclodextrin. | Wu, D. and Hurtubise, RJ. 1993. Talanta. 40: 901-7. PMID: 18965725
- Determination of 1-naphthol and 2-naphthol from environmental waters by magnetic solid phase extraction with Fe@MgAl-layered double hydroxides nanoparticles as the adsorbents prior to high performance liquid chromatography. | Zhou, Q., et al. 2016. J Chromatogr A. 1441: 1-7. PMID: 26965650
- Enhanced degradation of 1-naphthol in landfill leachate using Arthrobacter sp. | Hu, W., et al. 2019. Environ Technol. 40: 835-842. PMID: 29168925
- Radical scavenging effects of 1-naphthol, 2-naphthol, and their sulfate-conjugates. | Sugahara, S., et al. 2018. J Toxicol Sci. 43: 213-221. PMID: 29540655
- Three Spectrophotometric Methods for Quantitative Analysis of Duloxetine in Presence of its Toxic Impurity: 1-Naphthol. | Naguib, IA., et al. 2020. J AOAC Int. 103: 972-979. PMID: 33241329
- A novel covalent triazine framework developed for efficient determination of 1-naphthol in water. | Yang, L., et al. 2021. Environ Sci Pollut Res Int. 28: 31185-31194. PMID: 33598837
- Coinducible Catabolism of 1-Naphthol via Synergistic Regulation of the Initial Hydroxylase Genes in Sphingobium sp. Strain B2. | Huang, J., et al. 2021. Appl Environ Microbiol. 87: PMID: 33771783
- Phosphate-triggered ratiometric fluoroimmunoassay based on nanobody-alkaline phosphatase fusion for sensitive detection of 1-naphthol for the exposure assessment of pesticide carbaryl. | Chen, ZJ., et al. 2022. J Hazard Mater. 424: 127411. PMID: 34629198
- Structural study of 1- and 2-naphthol: new insights into the non-covalent H-H interaction in cis-1-naphthol. | Hazrah, AS., et al. 2022. Phys Chem Chem Phys. 24: 3722-3732. PMID: 35080568
- Comparative study on the removal of 1- naphthol and 2-naphthol by ferrate (VI): Kinetics, reaction mechanisms and theoretical calculations. | Qi, Y., et al. 2023. Chemosphere. 336: 139189. PMID: 37307926
- Quantitative analysis of naphthalene, 1-naphthol and 2-naphthol at nanomol levels in geothermal fluids using SPE with HPLC. | Sajkowski, L., et al. 2023. MethodsX. 11: 102244. PMID: 37388165
- Metabolism of 1-naphthol by tyrosinase. | Doherty M, D., et al. 1985. Biochem Pharmacol. 34: 3167-72. PMID: 3929786
- Conjugation of 1-naphthol in human gastric epithelial cells. | Déchelotte, P., et al. 1993. Gut. 34: 177-80. PMID: 8432468
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Naphthol, 25 g | sc-213374 | 25 g | $49.00 | |||
1-Naphthol, 100 g | sc-213374A | 100 g | $243.00 |