3147-75-9
3147-75-9
Chemical Structure
Octrizole
Synonym(s): UV-329
- CAS No.: 3147-75-9
- Formula:C20H25N3O
- Molecular Weight:323.43
IUPAC Name: 2-(2H-benzo[d][1,2,3]triazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol
InChIKey: IYAZLDLPUNDVAG-UHFFFAOYSA-N
SMILES: OC1=CC=C(C(C)(CC(C)(C)C)C)C=C1N2N=C3C=CC=CC3=N2
Biological Activity: Octrizole (UV-329) is a UV screener/stabilizer. Octrizole can prevent products from yellowing and degradation. Octrizole exhibits significant cytotoxicity to MVLN cells at concentrations higher than 50 μM and has no obvious estrogenic activity[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Octrizole | 99.67% | Octrizole (UV-329) is a UV screener/stabilizer. Octrizole can prevent products from yellowing and degradation. Octrizole exhibits significant cytotoxicity to MVLN cells at concentrations higher than 50 μM and has no obvious estrogenic activity. | ||||||||||||||||||||
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Octrizole (Standard) | ≥98% | Octrizole (Standard) (UV-329 (Standard)) is the analytical standard of Octrizole (HY-W009160). This product is intended for research and analytical applications. Octrizole (UV-329) is a UV screener/stabilizer. Octrizole can prevent products from yellowing and degradation. Octrizole exhibits significant cytotoxicity to MVLN cells at concentrations higher than 50 μM and has no obvious estrogenic activity. | ||||||||||||||||||||
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Octrizole-13C6 | Octrizole-13C6 is 13C labeled Octrizole. | |||||||||||||||||||||
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Octrizole-d4 | Octrizole-d4 (UV-329-d4) is deuterium labeled Octrizole (HY-W009160). Octrizole (UV-329) is a UV screener/stabilizer. Octrizole can prevent products from yellowing and degradation. Octrizole exhibits significant cytotoxicity to MVLN cells at concentrations higher than 50 μM and has no obvious estrogenic activity. | |||||||||||||||||||||
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References
- [1]. Feng H, et al. Estrogenic activity of benzotriazole UV stabilizers evaluated through in vitro assays and computational studies. Sci Total Environ. 2020 Jul 20;727:138549. [Content Brief]
- [2]. Lopez-Alvarado P, et al. New synthetic applications of aryllead triacetates. N-arylation of azoles. The Journal of Organic Chemistry, 1995, 60(17): 5678-5682.
