P2126

L-Phenylalanine

≥98%

• Synonyme(s) : (S)-2-Amino-3-phenylpropionic acid
• Formule linéaire : C₆H₅CH₂CH(NH₂)CO₂H
• Numéro CAS: 63-91-2
• Poids moléculaire : 165.19
• NACRES: NA.26
• PubChem Substance ID: 24898274
• eCl@ss: 32160406
• UNSPSC Code: 12352209
• EC Number: 200-568-1
• MDL number: MFCD00064227
• Beilstein/REAXYS Number: 1910408

Propriétés

• Nom du produit: L-Phenylalanine, reagent grade, ≥98%
• grade: reagent grade
• Quality Segment: 200
• assay: ≥98%
• form: powder or crystals
• color: white to off-white
• mp: 270-275 °C (dec.) (lit.)
• solubility: 1 M NH4OH: 50 mg/mL, clear, colorless
• application(s): detection
• SMILES string: N[C@@H](Cc1ccccc1)C(O)=O
• InChI: 1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1
• InChI key: COLNVLDHVKWLRT-QMMMGPOBSA-N
• Gene Information: human ... CA1(759), CA14(23632), CA2(760), CA4(762), CA5A(763), CA7(766)

Description

Application

L-Phenylalanine has been used in Fluo-4 Ca²⁺-assay in a study to demonstrate that G-protein coupled receptor 139 reference surrogate agonists 1a and 7c and L-phenylalanine share a common binding site. It has also been used to spike blood samples to study the effect of dried blood spots on newborn screening.

Biochem/physiol Actions

L-Phenylalanine is an essential aromatic amino acid. It has a role in metabolism as it forms a starting point for many pathways. This neutral amino acid is a precursor for tyrosine, epinephrine, dopamine and norepinephrine.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)