(S)-(+)-1,2-Propanediol

CAS : 4254-15-3

Ref. 3D-FP60219

Informations sur le produit

• Nom: (S)-(+)-1,2-Propanediol
• Synonymes: (S)-(+)-1,2-Dihydroxypropane(S)-(+)-Propylene Glycol, (+)-1,2-Propanediol, (2S)-1,2-Propanediol, (2S)-Propane-1,2-diol, (S)-(+)-1,2-propanediol, (S)-(+)-Propane-1,2-diol, (S)-(+)-Propylene glycol, (S)-2-Hydroxy-1-propanol, (S)-2-Hydroxypropanol, 1,2(S)-Propanediol, 1,2-Propanediol, (2S)-, 1,2-Propanediol, (S)-, 3-Deoxy-sn-glycerol, <span class="text-smallcaps">L</span>-(+)-Propanediol, <span class="text-smallcaps">L</span>-(+)-Propylene glycol, <span class="text-smallcaps">L</span>-1,2-Propanediol, d-Propylene glycol
• CAS: 4254-15-3

Description

(S)-(+)-1,2-Propanediol is a diol that is a chemical compound with the molecular formula HOCHCHOH. It has an asymmetric carbon atom and can exist as two enantiomers (S)-(+)-1,2-propanediol and (R)-(-)-1,2-propanediol. The compound is produced in the laboratory by oxidation of propylene with hydrogen peroxide in the presence of a metal catalyst. It undergoes dehydration reactions to form sugars such as erythritol and xylitol. This process also occurs naturally in some plants and bacteria where glucose is oxidized to form glycerol. The conversion of propane-1,2-diol to glycerol is catalyzed by alcohol dehydrogenase from yeast or fungi such as Candida boidinii or Candida kefyr. It also reacts with other molecules such as proteins via amide formation to form new compounds called a

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 76.09 g/mol
• Formule: C₃H₈O₂
• Degré de pureté: Min. 98%
• Couleur/Forme: Colorless Slightly Yellow Clear Liquid