Molecular structure of 3,5-Di-tert-butyl-4-hydroxybenzaldehyde, CAS Number: 1620-98-0
3,5-Di-tert-butyl-4-hydroxybenzaldehyde (CAS 1620-98-0)
CAS Number:
1620-98-0
Molecular Weight:
234.33
Molecular Formula:
C15H22O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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3,5-Di-tert-butyl-4-hydroxybenzaldehyde (DTBHB) is a versatile chemical compound extensively employed in scientific research due to its wide range of applications. Derived from benzaldehyde, 3,5-Di-tert-butyl-4-hydroxybenzaldehyde serves as a valuable reagent in organic synthesis. 3,5-Di-tert-butyl-4-hydroxybenzaldehyde has functioned as an antioxidant, exhibiting the ability to scavenge free radicals and mitigate oxidative stress. Moreover, it is believed to impede the activity of specific enzymes implicated in cell proliferation and apoptosis.
3,5-Di-tert-butyl-4-hydroxybenzaldehyde (CAS 1620-98-0) References
- High Stabilities of Di(1-azulenyl)(4-hydroxyphenyl)methyl Hexafluorophosphates and Polarized Properties of alpha,alpha-Di(1-azulenyl)-1,4-benzoquinone Methides. | Ito, S., et al. 1997. J Org Chem. 62: 2423-2431. PMID: 11671576
- Analysis of the antioxidant butylated hydroxytoluene (BHT) in water by means of solid phase extraction combined with GC/MS. | Fries, E. and Püttmann, W. 2002. Water Res. 36: 2319-27. PMID: 12108724
- Sodium-coupled ATP synthesis in the bacterium Vitreoscilla. | Efiok, BJ. and Webster, DA. 1992. Arch Biochem Biophys. 292: 102-6. PMID: 1309288
- Monitoring of BHT-quinone and BHT-CHO in the gas of capsules of Asclepias physocarpa. | Ma, BJ., et al. 2006. Z Naturforsch C J Biosci. 61: 458-60. PMID: 16869508
- Oxidation of synthetic phenolic antioxidants during water chlorination. | Rodil, R., et al. 2012. J Hazard Mater. 199-200: 73-81. PMID: 22093692
- Aminoalkyl functionalization of dextran for coupling of bioactive molecules and nanostructure formation. | Fiege, K., et al. 2013. Carbohydr Polym. 95: 569-77. PMID: 23618308
- Cross-conjugated hexaphyrins and their bis-rhodium complexes. | Naoda, K., et al. 2014. Chemistry. 20: 7698-705. PMID: 24805261
- Toxicological effects of Sphaeranthus indicus Linn. (Asteraceae) leaf essential oil against human disease vectors, Culex quinquefasciatus Say and Aedes aegypti Linn., and impacts on a beneficial mosquito predator. | Chellappandian, M., et al. 2018. Environ Sci Pollut Res Int. 25: 10294-10306. PMID: 28455566
- Crystal structure and DFT study of (E)-2,6-di-tert-butyl-4-{[2-(pyridin-2-yl)hydrazin-1-yl-idene)meth-yl}phenol. | Faizi, MSH., et al. 2017. Acta Crystallogr E Crystallogr Commun. 73: 1449-1452. PMID: 29250356
- Contaminants migrating from crossed-linked polyethylene pipes and their effect on drinking water odour. | Kalweit, C., et al. 2019. Water Res. 161: 341-353. PMID: 31212240
- Na(+)-translocating cytochrome bo terminal oxidase from Vitreoscilla: some parameters of its Na+ pumping and orientation in synthetic vesicles. | Park, C., et al. 1996. Biochemistry. 35: 11895-900. PMID: 8794772
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3,5-Di-tert-butyl-4-hydroxybenzaldehyde, 5 g | sc-266925 | 5 g | $47.00 |