446424
3,5-二叔丁基-4-羟基苯甲醇
97%
别名:
3,5-Di-tert-butyl-4-hydroxyphenylmethanol, 4-Hydroxymethyl-2,6-di-tert-butylphenol
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关于此项目
线性分子式:
HOC6H2[C(CH3)3]2CH2OH
化学文摘社编号:
分子量:
236.35
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-815-6
MDL number:
产品名称
3,5-二叔丁基-4-羟基苯甲醇, 97%
InChI key
HNURKXXMYARGAY-UHFFFAOYSA-N
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
SMILES string
CC(C)(C)c1cc(CO)cc(c1O)C(C)(C)C
assay
97%
form
solid
mp
139-141 °C (lit.)
functional group
hydroxyl
Quality Level
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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.
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.
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
O L Brekke et al.
Cytokine, 4(4), 269-280 (1992-07-01)
The effect of commonly used food antioxidants on recombinant tumor necrosis factor alpha (rTNF-alpha)-induced cytotoxicity, growth enhancement and adhesion has been evaluated. Butylated hydroxyanisole (BHA) and 4-hydroxymethyl-2,6-di-t-butylphenol (HBP) were the only two of nine antioxidants that completely inhibited rTNF-alpha-induced cytotoxicity
L R Barclay et al.
Biochimica et biophysica acta, 1328(1), 1-12 (1997-08-14)
Phenolic antioxidants of the hydroxychroman class, alpha-tocopherol (alpha-TOC) and 2,2,5,6,7-pentamethyl-6-hydroxychroman (PMHC), and the hindered phenols 2,3-dihydro-5-hydroxy-2,2,4-trimethylnaphtho[1,2-b]furan (NFUR), 2,6-di-tert-butyl-4-methoxyphenol (DBHA), and 2,6-di-tert-butyl-4-methyl phenol (BHT), were delivered into oxidizable (ACCEPTOR) liposomes of dilinoleoylphosphatidylcholine (DLPC) or 1-palmitoyl-2-linoleoyl-phosphatidylcholine (PLPC) from saturated DONOR liposomes of
REACTION OF SEVEN-AND EIGHT-MEMBERED CYCLIC PHOSPHOROCHLORIDITES WITH 3, 5-DI-tert-BUTYL-4-HYDROXYBENZYL ALCOHOL: FACILE P [sbnd] C BOND FORMATION.
Odorisio PA, et al.
Phosph. Sulfur Relat. Elem., 20(3), 273-277 (1984)
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)
Synthesis of new polymeric antioxidants.
Oh DR, et al.
Bull. Korean Chem. Soc., 22(6), 629-632 (2001)
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