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Merck
CN

34712

3,5-Di-tert-butyl-4-hydroxybenzoic acid

purum, ≥98.0% (T)

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About This Item

Linear Formula:
[(CH3)3C]2C6H2(OH)CO2H
CAS Number:
Molecular Weight:
250.33
EC Number:
215-823-2
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
2216948
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grade

purum

assay

≥98.0% (T)

mp

206-209 °C

SMILES string

CC(C)(C)c1cc(cc(c1O)C(C)(C)C)C(O)=O

InChI

1S/C15H22O3/c1-14(2,3)10-7-9(13(17)18)8-11(12(10)16)15(4,5)6/h7-8,16H,1-6H3,(H,17,18)

InChI key

YEXOWHQZWLCHHD-UHFFFAOYSA-N

Regulatory Information

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Karyophyllis C Tsiakitzis et al.
Journal of medicinal chemistry, 52(22), 7315-7318 (2009-10-30)
Agents against biologic stress were designed, containing GABA esterified with lorazepam and amidated with (R)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (5) or 3,5-di-tert-butyl-4-hydroxybenzoic acid (6). Compounds 5 and 6 inhibited lipid peroxidation, IC(50) 1.1 and 24 microM. Oxidative damage accompanied stress, 5 and 6
Bo Tao et al.
Journal of analytical methods in chemistry, 2020, 8869576-8869576 (2020-07-14)
The infusion bag is mainly made up of polyolefin polymer. Antioxidants are usually added to these polymer materials in the production process to prevent the materials from aging and enhance the stability of the materials. Because of the potential harm
Gonzalo García et al.
European journal of medicinal chemistry, 50, 90-101 (2012-02-18)
We report new examples of a series of losartan-hydrocaffeic hybrids that bear novel ester, amide and amine linkers. These compounds were made by linking hydrocaffeic acid to the side chain of losartan at the C-5 position of the imidazole ring

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