4528-07-8

Basic information

• Product Name: N-(2,4-Dinitrophenyl)-L-glutamic acid
• Synonyms: (2S)-2-(2,4-Dinitrophenylamino)pentanedioic acid;(2S)-N-(2,4-Dinitrophenyl)glutamic acid;(S)-2-[(2,4-Dinitrophenyl)amino]pentanedioic acid;DNP-L-Glutamic acid;N-(2,4-Dinitrophenyl)-L-glutamic acid
• CAS NO: 4528-07-8
• Molecular Formula: C₁₁H₁₁N₃O₈
• Molecular Weight: 313.22
• Mol File: 4528-07-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2,4-Dinitrophenyl)-L-glutamic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,4-Dinitrophenyl)-L-glutamic acid(4528-07-8)
• EPA Substance Registry System: N-(2,4-Dinitrophenyl)-L-glutamic acid(4528-07-8)

Safety Data

• Hazardous Substances Data: 4528-07-8(Hazardous Substances Data)

Upstream product

• 56-86-0 L-glutamic acid 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 1655-48-7 N-(2,4-dinitrophenyl)-D,L-glutamic acid 

Relevant articles and documents

Direct resolution of optically active isomers on chiral packings containing ergoline skeletons. 5. Enantioseparation of amino acid derivatives

A new procedure for ergot alkaloid-based chiral stationary phase preparation is described. Synthesis is based on bonding the allyl derivative of terguride to mercaptopropylsilanized silica gel. The packing exhibits higher content of chiral selector, stability, reproducibility, and enantioselectivity toward amino acids compared to that previously studied. The chromatographic behavior of amino acids with different side chains and substituent groups is investigated in order to obtain a deeper insight into the enantiodiscriminative mechanism as well as to determine the limitations and strengths of terguride as a chiral selector for this class of compounds. A variety of factors, including mobile phase parameters such as pH, ionic strength, content and nature of organic modifier, and temperature, are examined. A new procedure for ergot alkaloid-based chiral stationary phase preparation is described. Synthesis is based on bonding the allyl derivative of terguride to mercaptopropylsilanized silica gel. The packing exhibits higher content of chiral selector, stability, reproducibility, and enantioselectivity toward amino acids compared to that previously studied. The chromatographic behavior of amino acids with different side chains and substituent groups is investigated in order to obtain a deeper insight into the enantiodiscriminative mechanism as well as to determine the limitations and strengths of terguride as a chiral selector for this class of compounds. A variety of factors, including mobile phase parameters such as pH, ionic strength, content and nature of organic modifier, and temperature, are examined.