2,6-Bis(hydroxymethyl)-p-cresol

CAS : 91-04-3

Ref. 3D-FB34747

Informations sur le produit

• Nom: 2,6-Bis(hydroxymethyl)-p-cresol
• Synonymes: (2-Hydroxy-5-methyl-1,3-phenylene)dimethanol, 1,3-Benzenedimethanol, 2-hydroxy-5-methyl-, 2,3-Bis(Hydroxymethyl)-4-Methylphenol, 2,6-Bis(Hydroxymethyl)-4-Methylphenol, 2,6-Di(Hydroxymethyl)-4-Methylphenol, 2,6-Di(hydroxymethyl)-p-cresol, 2,6-Dimethylol-4-methylphenol, 2,6-Dimethylol-p-cresol, 26Dmpc, 4-Methyl-2,6-bis(hydroxymethyl)phenol, AV Lite 26DMPC, Dml-Pc, NSC 15838, α¹,α³,2-Trihydroxymesitylene, α¹,α³-Mesitylenediol, 2-hydroxy-, α1,α3-Mesitylenediol, 2-hydroxy-, 2-Hydroxy-5-methyl-1,3-benzenedimethanol

Description

2,6-Bis(hydroxymethyl)-p-cresol (BHMC) is a cross-linking agent that reacts with the hydroxyl groups of polymers to form covalent bonds. This reaction is irreversible and has been shown to be effective in thermal expansion applications. BHMC is insoluble in water and so can be used as a proton donor for the synthesis of polymer hydrogels. BHMC has also been used as a molecular modeling probe for studying protein structure and function. This compound reacts with nucleophiles by nucleophilic attack on the carbonyl carbon atom, producing an intermediate that tautomerizes to the corresponding enone. The reaction mechanism involves formation of a tetranuclear transition state followed by acid catalysis. Functional groups such as -OH, -NH2, or -COOH are required for this reaction to occur. NMR spectra have shown that there are three different chemical structures

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 168.19 g/mol
• Formule: C₉H₁₂O₃
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C9H12O3/c1-6-2-7(4-10)9(12)8(3-6)5-11/h2-3,10-12H,4-5H2,1H3
• Code InChI: InChIKey=KUMMBDBTERQYCG-UHFFFAOYSA-N
• SMILES: Cc1cc(CO)c(O)c(CO)c1