446424

3,5-Di-tert-butyl-4-Hydroxybenzylalkohol

97%

• Synonym(e): 3,5-Di-tert-butyl-4-hydroxyphenylmethanol, 4-Hydroxymethyl-2,6-di-tert-butylphenol
• Lineare Formel: HOC₆H₂[C(CH₃)₃]₂CH₂OH
• CAS-Nummer: 88-26-6
• Molekulargewicht: 236.35
• EG-Nummer: 201-815-6
• MDL-Nummer: MFCD00017254
• UNSPSC-Code: 12352100
• PubChem Substanz-ID: 24868276
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: 97%
• Form: solid
• mp (Schmelzpunkt): 139-141 °C (lit.)
• Funktionelle Gruppe: 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
• InChIKey: HNURKXXMYARGAY-UHFFFAOYSA-N

Beschreibung

Allgemeine Beschreibung

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]

Anwendung

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.

Sicherheitshinweise

• H-Sätze: H412
• P-Sätze: P273 - P501
• Gefahreneinstufungen: Aquatic Chronic 3
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves