446424

3,5-Di-tert-butyl-4-hydroxybenzyl alcohol

97%

• Sinónimos: 3,5-Di-tert-butyl-4-hydroxyphenylmethanol, 4-Hydroxymethyl-2,6-di-tert-butylphenol
• Fórmula lineal: HOC₆H₂[C(CH₃)₃]₂CH₂OH
• Número de CAS: 88-26-6
• Peso molecular: 236.35
• EC Number: 201-815-6
• MDL number: MFCD00017254
• UNSPSC Code: 12352100
• PubChem Substance ID: 24868276
• NACRES: NA.22

Propiedades

• 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

Descripción

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.

Información de seguridad

• hcodes: H412
• pcodes: P273 - P501
• Hazard Classifications: Aquatic Chronic 3
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• ppe: dust mask type N95 (US), Eyeshields, Gloves