446424

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

97%

• Synonyme(s) : 3,5-Di-tert-butyl-4-hydroxyphenylmethanol, 4-Hydroxymethyl-2,6-di-tert-butylphenol
• Formule linéaire : HOC₆H₂[C(CH₃)₃]₂CH₂OH
• Numéro CAS: 88-26-6
• Poids moléculaire : 236.35
• Numéro CE : 201-815-6
• Numéro MDL: MFCD00017254
• Code UNSPSC : 12352100
• ID de substance PubChem : 24868276
• Nomenclature NACRES : NA.22

Propriétés

• Essai: 97%
• Forme: solid
• Pf: 139-141 °C (lit.)
• Groupe fonctionnel: hydroxyl
• Chaîne SMILES: 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
• Clé InChI: HNURKXXMYARGAY-UHFFFAOYSA-N

Description

Description générale

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. [1]

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.

Informations sur la sécurité

• Mentions de danger: H412
• Conseils de prudence: P273 - P501
• Classification des risques: Aquatic Chronic 3
• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Gloves