Molecular structure of 1,4-Dimethylnaphthalene, CAS Number: 571-58-4
1,4-Dimethylnaphthalene (CAS 571-58-4)
CAS Number:
571-58-4
Purity:
≥95%
Molecular Weight:
156.22
Molecular Formula:
C12H12
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1,4-Dimethylnaphthalene is an aromatic hydrocarbon obtained from naphthalene and finds wide-ranging applications in industry. It serves as a solvent, plays a role in the production of resins, and acts as a fuel additive. Additionally, it functions as an intermediate in the synthesis of various compounds, including dyes. Furthermore, researchers have investigated its potential as a pesticide and herbicide. As a model compound, it has been extensively employed in studies exploring the structure and reactivity of aromatic hydrocarbons, and as a reagent in the synthesis of diverse compounds.
1,4-Dimethylnaphthalene (CAS 571-58-4) References
- Disposition and metabolism of 1,4-dimethylnaphthalene in rat. | Kilanowicz, A., et al. 2000. Int J Occup Med Environ Health. 13: 325-34. PMID: 11276846
- Characterization of Sphingomonas aldehyde dehydrogenase catalyzing the conversion of various aromatic aldehydes to their carboxylic acids. | Peng, X., et al. 2005. Appl Microbiol Biotechnol. 69: 141-50. PMID: 15812642
- Disorder-to-order transition of 1,4-dimethylnaphthalene: Formation of molecular complex with water and p-xylene on Al2O3 (0001). | Evans, MA., et al. 2006. J Phys Chem B. 110: 19758-62. PMID: 17020358
- Yields of glyoxal and ring-cleavage co-products from the OH radical-initiated reactions of naphthalene and selected alkylnaphthalenes. | Nishino, N., et al. 2009. Environ Sci Technol. 43: 8554-60. PMID: 20028051
- The sprout inhibitors chlorpropham and 1,4-dimethylnaphthalene elicit different transcriptional profiles and do not suppress growth through a prolongation of the dormant state. | Campbell, MA., et al. 2010. Plant Mol Biol. 73: 181-9. PMID: 20135197
- Liquid phase separation of polyaromatics on [Cu2(BDC)2(dabco)]. | Maes, M., et al. 2011. Langmuir. 27: 9083-7. PMID: 21696201
- The sprout inhibitor 1,4-dimethylnaphthalene induces the expression of the cell cycle inhibitors KRP1 and KRP2 in potatoes. | Campbell, MA., et al. 2012. Funct Integr Genomics. 12: 533-41. PMID: 22113341
- Functionalized derivatives of 1,4-dimethylnaphthalene as precursors for biomedical applications: synthesis, structures, spectroscopy and photochemical activation in the presence of dioxygen. | Posavec, D., et al. 2012. Org Biomol Chem. 10: 7062-9. PMID: 22847738
- Changes in gene expression in potato meristems treated with the sprout suppressor 1,4-dimethylnaphthalene are dependent on tuber age and dormancy status. | Campbell, MA., et al. 2020. PLoS One. 15: e0235444. PMID: 32614863
- Photothermally Responsive Conjugated Polymeric Singlet Oxygen Carrier for Phase Change-Controlled and Sustainable Phototherapy for Hypoxic Tumor. | Li, G., et al. 2020. Research (Wash D C). 2020: 5351848. PMID: 33103118
- Review of the existing maximum residue levels for 1,4-dimethylnaphthalene according to Article 12 of Regulation (EC) No 396/2005. | , ., et al. 2021. EFSA J. 19: e06597. PMID: 34035863
- Photothermal Responsive Singlet Oxygen Nanocarriers for Hypoxic Cancer Cell Ablation. | Zhu, T., et al. 2021. Chembiochem. 22: 2546-2552. PMID: 34101959
- Inhibition of DMBA carcinogenesis of hamster buccal pouch by phenanthrene and dimethylnaphthalene. | Malament, DS. and Shklar, G. 1981. Carcinogenesis. 2: 723-9. PMID: 6793258
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,4-Dimethylnaphthalene, 5 g | sc-237765 | 5 g | $111.00 |