a-Phenyllactic acid

CAS : 515-30-0

Ref. 3D-FP52536

Informations sur le produit

• Nom: a-Phenyllactic acid
• Synonymes: 2-Hydroxy-2-phenylpropanoic acidAtrolactic acid, (+/-)-2-Hydroxy-2-phenylpropionic acid hemihydrate, (+/-)-2-Phenyllactic acid hemihydrate, (+/-)-Atrolactic acid hemihydrate, (2R)-2-hydroxy-2-phenylpropanoate, (2S)-2-hydroxy-2-phenylpropanoate, (RS)-2-Phenyllactic acid, (±)-2-Hydroxy-2-phenylpropionic acid, (±)-α-Hydroxy-α-methylbenzeneacetic acid, 2-Hydroxy-2-phenyl-2-methylacetic acid, 2-Hydroxy-2-phenylpropanoic acid, 2-Phenyl-2-hydroxypropionic acid, 2-Phenyllactic Acid, <span class="text-smallcaps">DL</span>-2-Phenyllactic acid, <span class="text-smallcaps">DL</span>-Atrolactic acid, <span class="text-smallcaps">DL</span>-α-Methylmandelic acid, <span class="text-smallcaps">DL</span>-α-Phenyllactic acid, Atrolactic acid, Atrolacticacid, Atrolactinic acid, Benzeneacetic acid, α-hydroxy-α-methyl-, Mandelic acid, α-methyl-, NSC 128998, NSC 401846, alpha-Hydroxy-2-methylbenzeneacetic acid, dl-Atrolactic acid, α-Hydroxy-2-phenylpropionic acid, α-Hydroxy-α-phenylpropionic acid, α-Methylmandelic acid, α-Phenyllactic acid

Description

a-Phenyllactic acid is a fatty acid that is naturally found in the body. It is an intermediate of the biosynthesis of other compounds, such as pyruvic acid and lactic acid. It has been shown to be a metabolite of phenylalanine and tyrosine in urine samples by electrochemical impedance spectroscopy. a-Phenyllactic acid can be synthesized from ethylene diamine and galacturonic acid, which can be obtained from natural sources such as fruit juices or sugar cane molasses. The product may be used for neutralizing acidic substances, such as hydrochloric acid or sodium carbonate, because it is insoluble in water.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 166.17 g/mol
• Formule: C₉H₁₀O₃
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C9H10O3/c1-9(12,8(10)11)7-5-3-2-4-6-7/h2-6,12H,1H3,(H,10,11)
• Code InChI: InChIKey=NWCHELUCVWSRRS-UHFFFAOYSA-N
• SMILES: CC(O)(C(=O)O)c1ccccc1