DL-3-(2-Naphthyl)alanine

Product Details

CAS No:14108-60-2

MF:C13H13NO2

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:KGS

Synonyms:3-(2-NAPHTHYL)-DL-ALANINE;2-AMINO-3-NAPHTHALEN-2-YL-PROPIONIC ACID;H-DL-NAL(2)-OH;H-DL-ALA(2-NAPH)-OH;H-DL-ALA(2-NAPHTHYL)-OH;H-DL-2-NAL-OH;DL-3-(2-NAPHTHYL)ALANINE;2-amino-3-naphthalen-2-ylpropanoic acid; 14108-60-2; DTXSID50290595; alpha-Amino-2-naphthalenepropanoic acid; RefChem:1076439; DTXCID30884476; H-DL-2-NAL-OH; 2-Amino-3-(naphthalen-2-yl)propanoic acid; 3-(2-Naphthyl)-DL-alanine; 2-amino-3-naphthalen-2-ylpropanoic acid; MFCD00070216; DL-2-Naphthylalanine; 6960-34-5; 2-Naphthalenepropanoic acid, alpha-amino-; 3-(2-Naphthyl)alanine; 2-Naphthalenealanine; 3-Naphthalen-2-ylalanine; beta-naphtyl alanine; 3-(2-naphthyl)-alanine; 3-(2-Naphthyl)alanine #; 2-AMINO-3-NAPHTHALEN-2-YL-PROPIONIC ACID; SCHEMBL93304; 3-(Naphthalen-2-yl)alanine; H-DL-ALA(2-NAPH)-OH; CHEMBL3272605; SCHEMBL29401985; SCHEMBL29584308; CHEBI:229533; NSC69865; DL-3-(2-NAPHTHYL)-ALANINE; NSC-69865; AKOS000191768; AKOS016843550; AB01739; AB02815; 2-Amino-3-naphthalen-2-ylpropionic acid; AS-63072; SY035605; DB-018115; DB-346705; CS-0146966; 2-AMINO-3-(2-NAPHTHYL)PROPANOIC ACID; EN300-57632; A50367; DL-2-Amino-3-(naphthalen-2-yl)propanoic acid; F237712

Product application:DL-3-(2-Naphthyl)alanine,14108-60-2,DL-2-Amino-3-(2-naphthyl)propanoic acid,3-(2-Naphthyl)-DL-alanine,2-Naphthylalanine,Unnatural aromatic amino acid,Non-proteinogenic amino acid,Pharmaceutical grade DL-3-(2-Naphthyl)alanine,Peptide modification building block,Peptidomimetic intermediate,Antitumor peptide building block,Somatostatin analogue precursor,Chiral resolution starting material,L-2-Naphthylalanine precursor,D-2-Naphthylalanine precursor,Cosmetic peptide raw material,Anti-aging peptide monomer,Asymmetric catalyst ligand intermediate,Fluorescent probe building block,Biomedical polymer monomer,Fine chemical raw material,High purity DL-3-(2-Naphthyl)alanine 99%,DL-3-(2-Naphthyl)alanine manufacturer China,CAS 14108-60-2 supplier,Suzhou Health Chemicals unnatural amino acids,2-Naphthylalanine wholesale bulk export

 

DL-3-(2-Naphthyl)alanine serves as an indispensable, high-purity unnatural aromatic amino acid building block, versatile peptidomimetic intermediate, and specialized chiral synthon extensively utilized across peptide biopharmaceuticals, asymmetric catalytic synthesis, high-performance cosmetic peptides, fluorescent sensor materials, and diverse fine chemical engineering sectors. In active pharmaceutical ingredient (API) manufacturing and therapeutic peptide engineering, functioning as a bulky, hydrophobic analogue of natural phenylalanine, the incorporation of DL-3-(2-Naphthyl)alanine or its optically resolved D- and L-enantiomers into peptide sequences significantly enhances hydrophobic pi-pi stacking interactions within target receptor binding pockets; furthermore, its rigid bicyclic naphthalene side chain imparts superior steric resistance against endogenous proteolytic cleavage, dramatically optimizing the metabolic stability, bioavailability, and pharmacokinetic profile of somatostatin analogues, targeted oncology peptides, antithrombotic peptidomimetics, and antimicrobial peptides. In asymmetric organic synthesis and organocatalysis, it is an essential chiral starting material for preparing chiral organocatalysts, asymmetric ligands, and chiral stationary phases for chromatographic separation. In cosmeceutical formulation and personal care chemistry, it functions as a critical synthetic monomer for bioactive anti-aging biomimetic peptides and collagen-stimulating agents, promoting cutaneous rejuvenation and dermal barrier resilience. In optoelectronics and fluorescent biosensing, capitalizing on the intrinsic rigid fluorophore properties of the naphthalene core, it is widely utilized to design environmental fluorescent probes, macromolecular conformational markers, and functional optoelectronic copolymers. In specialty polymer resins, functional adhesives, and protective coatings, incorporation of this aromatic amino acid derivative elevates glass transition temperatures (Tg) and enhances thermal oxidation resistance. Furthermore, in functional textile modification, advanced leather topcoats, eco-friendly wood preservatives, and metallurgical corrosion inhibitor complexes for oilfield pipelines, structural derivatives based on DL-3-(2-Naphthyl)alanine deliver outstanding chemical durability, coordination capacity, and multi-industry versatility.