N, N-Dimethyl-L-phenylalanine

<strong>N,N-Dimethyl-L-phenylalanine</strong>_x000D_ <strong>Catalog number:</strong> B2015826_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 250 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 193.24_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> RT, dry_x000D_ <strong>Keywords:</strong> (2S)-2-(Dimethylamino)-3-phenylpropanoic acid, N,N-Dimethylphenylalanine_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Dimitrova P, Bart HJ. Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N,N-dimethyl-L-phenylalanine as the chiral additive for enantioselective amino acids separation Anal Chim Acta. 2010 Mar 17;663(1):109-16._x000D_ 2: Jia DX, Ai ZG, Xue YP, Zheng YG. Chiral ligand-exchange high-performance liquid chromatography with copper (II)-L-phenylalanine complexes for separation of 3,4-dimethoxy-α-methylphenylalanine racemes Anal Bioanal Chem. 2014 Nov;406(29):7687-94._x000D_ 3: Nikolić N, Veselinović D, Vucina J, Lingeman H, Karljiković-Rajić K. Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime J Pharm Biomed Anal. 2003 Aug 21;32(6):1159-66._x000D_ 4: Bortoluzzi M, Bresciani G, Marchetti F, Pampaloni G, Zacchini S. MoCl5 as an effective chlorinating agent towards α-amino acids: synthesis of α-ammonium-acylchloride salts and α-amino-acylchloride complexes Dalton Trans. 2015 Jun 7;44(21):10030-7._x000D_ 5: Biancalana L, Tuci G, Piccinelli F, Marchetti F, Bortoluzzi M, Pampaloni G. Vanadium(v) oxoanions in basic water solution: a simple oxidative system for the one pot selective conversion of l-proline to pyrroline-2-carboxylate Dalton Trans. 2017 Nov 7;46(43):15059-15069._x000D_ 6: Bhushan R, Tanwar S. Different approaches of impregnation for resolution of enantiomers of atenolol, propranolol and salbutamol using Cu(II)-L-amino acid complexes for ligand exchange on commercial thin layer chromatographic plates J Chromatogr A. 2010 Feb 19;1217(8):1395-8._x000D_ 7: Tong S, Shen M, Zhang H, Cheng D, Yan J. Modeling the retention mechanism for high-performance liquid chromatography with a chiral ligand mobile phase and enantioseparation of mandelic acid derivatives J Sep Sci. 2015 Jun;38(12):2085-92._x000D_ 8: Nikolić N, Veselinović D, Vladimirov S, Karljiković-Rajić K, Lingeman H. Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity J Pharm Biomed Anal. 2004 Feb 4;34(2):285-93._x000D_ 9: Bortoluzzi M, Hayatifar M, Marchetti F, Pampaloni G, Zacchini S. Synthesis of α-amino acidato derivatives of niobium and tantalum pentahalides and their conversion into iminium salts Inorg Chem. 2015 Apr 20;54(8):4047-55._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/10704122">10: Dolezalová M, Tkaczyková M. Direct high-performance liquid chromatographic determination of the enantiomeric purity of levodopa and methyldopa: comparison with pharmacopoeial polarimetric methods J Pharm Biomed Anal. 1999 Mar;19(3-4):555-67. </a>_x000D_ _x000D_ <strong>Products Related to N,N-Dimethyl-L-phenylalanine can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>