CAS 1620-98-0
:3,5-Di-tert-butyl-4-hydroxybenzaldehyde
Description:
3,5-Di-tert-butyl-4-hydroxybenzaldehyde, with the CAS number 1620-98-0, is an organic compound characterized by its aromatic structure featuring a hydroxyl group and an aldehyde functional group. It is a derivative of hydroxybenzaldehyde, specifically substituted with two tert-butyl groups at the 3 and 5 positions of the benzene ring, which significantly enhances its lipophilicity and steric hindrance. This compound is typically a white to pale yellow solid at room temperature and is known for its antioxidant properties, making it useful in various applications, including as a stabilizer in plastics and other materials. The presence of the hydroxyl group contributes to its reactivity, allowing it to participate in various chemical reactions, such as oxidation and esterification. Additionally, its bulky tert-butyl groups can influence its solubility and interaction with other molecules, making it a subject of interest in both synthetic and industrial chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C15H22O2
InChI:InChI=1S/C15H22O2/c1-14(2,3)11-7-10(9-16)8-12(13(11)17)15(4,5)6/h7-9,17H,1-6H3
InChI key:InChIKey=DOZRDZLFLOODMB-UHFFFAOYSA-N
SMILES:CC(C)(C)c1cc(cc(c1O)C(C)(C)C)C=O
Synonyms:- 2,6-Di-tert-Butyl-4-formylphenol
- 3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzaldehyde
- 3,5-Ditert-butyl-4-hydroxybenzaldehyde
- 3,5-di0T0butyl-4-hydroxybenzaldehyde*hemihydrate
- 4-Formyl-2,6-di-tert-butylphenol
- 4-Hydroxy-3,5-di-tert-butylbenzaldehyde
- Benzaldehyde, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-
- Benzaldehyde, 3,5-di-tert-butyl-4-hydroxy-
- NSC 14450
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Found 10 products.
3,5-Di-tert-butyl-4-hydroxybenzaldehyde
CAS:Formula:C15H22O2Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:234.343,5-Di-tert-butyl-4-hydroxybenzaldehyde, 98+%
CAS:<p>3,5-Di-tert-butyl-4-hydroxybenzaldehyde is employed as an OLED materials. It is also used as a pharmaceutical intermediate. The derivatives of this compound possess equipotent anti-inflammatory activities to indomethacin. This Thermo Scientific Chemicals brand product was originally part of the Alf</p>Formula:C15H22O2Purity:98+%Color and Shape:White to cream or pale yellow to yellow, Crystals or powder or crystalline powder or flakesMolecular weight:234.34Benzaldehyde, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-
CAS:Formula:C15H22O2Purity:98%Color and Shape:SolidMolecular weight:234.33403,5-Bis(tert-butyl)-4-hydroxybenzaldehyde
CAS:<p>3,5-Bis(tert-butyl)-4-hydroxybenzaldehyde</p>Formula:C15H22O2Purity:≥95%Color and Shape: pale yellow powderMolecular weight:234.33397g/mol3,5-Di-tert-butyl-4-hydroxybenzaldehyde
CAS:Controlled ProductFormula:C15H22O2Color and Shape:NeatMolecular weight:234.333,5-Di-tert-butyl-4-hydroxybenzylaldehyde
CAS:<p>3,5-Di-tert-butyl-4-hydroxybenzylaldehyde is a compound that can be used as an extraction solvent for solid phase microextraction (SPME) in analytical methods. This sample preparation technique is used to measure the amount of malonic acid in kidney bean samples, as well as to detect growth factors in cell cultures. 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde has been shown to be effective in wastewater treatment and has also been found to have anti-inflammatory properties. In addition, this compound was detected at low levels in urine samples from patients with inflammatory diseases. The mechanism of 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde's antiinflammatory activity may be due to its ability to inhibit oxidative DNA damage by reacting with hydrogen bonds.</p>Formula:C15H22O2Purity:Min. 95%Color and Shape:PowderMolecular weight:234.33 g/mol3,5-Di-tert-butyl-4-hydroxybenzaldehyde
CAS:Formula:C15H22O2Purity:95%Color and Shape:SolidMolecular weight:234.3393,5-Di-tert-butyl-4-Hydroxybenzaldehyde
CAS:Formula:C15H22O2Color and Shape:White To Off-White SolidMolecular weight:234.34Ref: 4Z-B-131014
Discontinued product
