Quality Level
assay
97%
form
solid
mp
139-141 °C (lit.)
functional group
hydroxyl
SMILES string
CC(C)(C)c1cc(CO)cc(c1O)C(C)(C)C
InChI
1S/C15H24O2/c1-14(2,3)11-7-10(9-16)8-12(13(11)17)15(4,5)6/h7-8,16-17H,9H2,1-6H3
InChI key
HNURKXXMYARGAY-UHFFFAOYSA-N
General description
3,5-di-tert-butyl-4-hydroxybenzyl alcohol also known as 4-Hydroxymethyl-2,6-di-tert-butylphenol that is commonly used as an antioxidant in the preparation of PMA-type bifunctional polymers.
Application
3,5-Di-tert-butyl-4-hydroxybenzyl alcohol can be used as a reactant to synthesize:
- 2,6-di-tert-butyl-4-(dodecylselanylmethyl)phenol and bis(3,5-di-tert-butyl-4-hydroxybenzyl) selenide by reacting with dodecaneselenolate and sodium selenide.
- Monomeric antioxidant by reacting with imidazole and N-[4-(chlorocarbonyl)phenyl]maleimide.
- Sulfur-containing butylated hydroxytoluene derivatives by reacting with aryl/alky dithiols.
- 3,5-Di-tert-butyl-4-hydroxybenzaldehyde by oxidation reaction using stabilized IBX.
Still not finding the right product?
Explore all of our products under 3,5-二叔丁基-4-羟基苯甲醇
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Melt-grafting of maleimides having hindered phenol group onto polypropylene.
Kim TH and Lee N.
Bull. Korean Chem. Soc., 24(12), 1809-1813 (2003)
X Guan et al.
Carcinogenesis, 16(10), 2575-2582 (1995-10-01)
The mouse pneumotoxicant and lung and liver tumor promoter butylated hydroxytoluene (BHT) was examined for its effects on gap junctional intercellular communication (GJIC) in mouse lung epithelial (C10) and rat liver epithelial (WB-F344) cell lines. GJIC, as measured by fluorescent
The antioxidant activity of 3, 5-di-tert-butyl-4-hydroxybenzyl derivatives.
Kim DH and Kummerow FA.
Journal of the American Chemical Society, 39(3), 150-155 (1962)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 446424-5G | 04061832287423 |
| 446424-25G | 04061835176878 |
| 446424-100G | 04065274213316 |