Molecular structure of 9-Methylcarbazole, CAS Number: 1484-12-4
9-Methylcarbazole (CAS 1484-12-4)
CAS Number:
1484-12-4
Molecular Weight:
181.23
Molecular Formula:
C13H11N
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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9-Methylcarbazole is a chemical compound that functions as a fluorescent dye in research and development applications. It is utilized to label and visualize specific molecules or structures within cells and tissues. The compound′s mechanism of action involves binding to target molecules or structures, emitting fluorescence when excited by specific wavelengths of light. This allows researchers to track and study the localization and movement of the labeled molecules or structures in various experimental assays. 9-Methylcarbazole can be used to detect and quantify specific biomolecules in biochemical assays, contributing to the understanding of molecular interactions and cellular processes. Its ability to emit fluorescence upon binding to target molecules may be useful for visualizing and analyzing biological samples in research and development applications.
9-Methylcarbazole (CAS 1484-12-4) References
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- Novel 3-substituted N-methylcarbazole-imidazolium salt derivatives: Synthesis and cytotoxic activity. | Li, YH., et al. 2018. Chem Biol Drug Des. 92: 1206-1213. PMID: 29430875
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- Graphene oxide modified magnetic polyamidoamide dendrimers based magnetic solid phase extraction for sensitive measurement of polycyclic aromatic hydrocarbons. | Tong, Y., et al. 2022. Chemosphere. 296: 134009. PMID: 35189186
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- Mutagenicity of substituted carbazoles in Salmonella typhimurium. | LaVoie, EJ., et al. 1982. Mutat Res. 101: 141-50. PMID: 7048081
- Metabolism of N-methylcarbazole by rat lung microsomes. | Ibe, BO. and Raj, JU. 1994. Exp Lung Res. 20: 207-22. PMID: 7925139
- Chemiexcitation in the peroxidative metabolism of N-methylcarbazole: mechanistic implications. | de Melo, MP. and Cilento, G. 1994. Photochem Photobiol. 59: 677-82. PMID: 8066126
- Inactivation of purified rat liver cytochrome P-450 2B1 and rabbit liver cytochrome P-450 2B4 by N-methylcarbazole. | Kuemmerle, SC., et al. 1994. Drug Metab Dispos. 22: 343-51. PMID: 8070309
- The mechanism of stimulation of NADPH oxidation during the mechanism-based inactivation of cytochrome P450 2B1 by N-methylcarbazole: redox cycling and DNA scission. | Shen, T. and Hollenberg, PF. 1994. Chem Res Toxicol. 7: 231-8. PMID: 8199313
- Bioassay of quinoline, 5-fluoroquinoline, carbazole, 9-methylcarbazole and 9-ethylcarbazole in newborn mice. | Weyand, EH., et al. 1993. Food Chem Toxicol. 31: 707-15. PMID: 8225128
- Microbial models of mammalian metabolism: involvement of cytochrome P450 in the N-demethylation of N-methylcarbazole by Cunninghamella echinulata. | Yang, W., et al. 1993. Xenobiotica. 23: 973-82. PMID: 8291265
- The formation of an N-hydroxymethyl intermediate in the N-demethylation of N-methylcarbazole in vivo and in vitro. | Gorrod, JW. and Temple, DJ. 1976. Xenobiotica. 6: 265-74. PMID: 936646
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
9-Methylcarbazole, 5 g | sc-227145 | 5 g | $136.00 |