P1751

D-Phenylalanine

≥98% (HPLC)

• Synonym(s): (R)-2-Amino-3-phenylpropionic acid
• Empirical Formula (Hill Notation): C₉H₁₁NO₂
• CAS Number: 673-06-3
• Molecular Weight: 165.19
• Beilstein: 2804068
• EC Number: 211-603-5
• MDL number: MFCD00004270
• UNSPSC Code: 12352209
• PubChem Substance ID: 24898241
• NACRES: NA.26

Properties

• product name: D-Phenylalanine, ≥98% (HPLC)
• Assay: ≥98% (HPLC)
• form: powder
• color: white to off-white
• mp: 273-276 °C
• application(s): cell analysis
• 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-/m1/s1
• InChI key: COLNVLDHVKWLRT-MRVPVSSYSA-N
• Gene Information: human ... CA1(759) , CA14(23632) , CA2(760) , CA4(762) , CA5A(763) , CA7(766)

Description

Application

<ul>
<li><strong>Paper Title: </strong> Supramolecular nanofibers co-loaded with dabrafenib and doxorubicin for targeted and synergistic therapy of differentiated thyroid carcinoma. D-Phenylalanine are used to improve the stability of peptides <em>in vivo</em> (Chen P et al., 2023).</li>
<li><strong>Paper Title: </strong> Mechanistic aspects of the transamination reactions catalyzed by D-amino acid transaminase from Haliscomenobacter hydrossis. This study focuses on the enzymatic roles of D-Phenylalanine in specific bacterial transamination processes, applicable in biocatalysis and synthetic biology (Bakunova AK et al., 2023).</li>
</ul>

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 1
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves