(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide Basic information
- Product Name:
- (S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide
- Synonyms:
-
- 1-FLUORO-2,4-DINITROPHENYL-5-L-ALANINE AMIDE
- Nα-(2,4-Dinitro-5-fluorophenyl)-L-alanine amide≥ 98% (HPLC)
- NALPHA-(5-FLUORO-2,4-DINITROPHENYL)-L-ALANINAMIDE
- N-ALPHA-(2,4-DINITRO-5-FLUOROPHENYL)-L-ALANINAMIDE
- N-ALPHA-(2,4-DINITRO-5-FLUOROPHENYL)-L-ALANINE AMIDE
- (2,4-Dinitro-5-fluorophenyl) L-Alaninamide
- Marfey's Reagent, 99%, for chiral derivatization
- Nalpha-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide [HPLC Labeling Reagent for e.e. Determination]
- CAS:
- 95713-52-3
- MF:
- C9H9FN4O5
- MW:
- 272.19
- Product Categories:
-
- proteinmod
- Amino Acids & Derivatives
- Aromatics
- Chiral Reagents
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Amino Group Labeling Reagents for HPLC
- Analytical Chemistry
- e.e. Determination (HPLC Labeling Reagents)
- Enantiomer Excess & Absolute Configuration Determination
- HPLC Labeling Reagents
- UV Detection (HPLC Labeling Reagents)
- Mol File:
- 95713-52-3.mol
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide Chemical Properties
- Melting point:
- 229 °C
- Boiling point:
- 544.5±50.0 °C(Predicted)
- Density
- 1.592±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- acetone: 10 mg/mL, clear, yellow
- form
- powder
- pka
- 15.61±0.50(Predicted)
- color
- yellow to orange
- optical activity
- [α]20/D +56±2°, c = 1% in acetone
- BRN
- 6820069
- InChIKey
- NEPLBHLFDJOJGP-BYPYZUCNSA-N
MSDS
- Language:English Provider:SigmaAldrich
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide Usage And Synthesis
Chemical Properties
Light yellow to yellow crystal or powder
Uses
FDAA was used as derivatizing reagent, in a study performed to understand unusual amino acids using reversed phase high performance liquid chromatography-electrospray ionization mass spectrometry (RPHPLC-ESI-MS).
Uses
N-α-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide is suitable for use for the derivatization of amino acids. glutamate and analine present in cell wall. Derivatized?D- and?L-amino acids can be resolved and quantitated by HPLC.
Uses
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide can be used for chiral amino acid analysis.
General Description
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent (CDA), has high enantioselectivity but low sensitivity as compared to other CDAs. It is generally used to assign the stereochemistry of amino acids in trace amounts.
Biochem/physiol Actions
N-α-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent and is used routinely to improve the detection of underivatized amino acids in high performance liquid chromatography. Its usage is effective in separating stereoisomer.
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMideSupplier
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(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide(95713-52-3)Related Product Information
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- 3-FLUORO-N-METHYLANILINE
- N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE
- 3,4-Diaminofluorobenzene
- (S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide
- N-(2-AMINO-ETHYL)-BENZENE-1,2-DIAMINE
- N-(2-NITRO-PHENYL)-ETHANE-1,2-DIAMINE
- 4-FLUORO-5-NITROBENZENE-1,2-DIAMINE
- (3-fluoro-4-nitrophenyl)methanamine
- 2,4-DIAMINOFLUOROBENZENE
- NALPHA-(5-FLUORO-2,4-DINITROPHENYL)-L-LEUCINAMIDE