71478
Nα-（2,4-二硝基-5-氟苯基）-L氨基丙酰胺
derivatization grade (chiral), LiChropur™, ≥99.0%
别名:
FDAA, Marfey 试剂
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关于此项目
经验公式（希尔记法）:
C9H9FN4O5
化学文摘社编号:
分子量:
272.19
UNSPSC Code:
23151816
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6820069
产品名称
Nα-（2,4-二硝基-5-氟苯基）-L氨基丙酰胺, derivatization grade (chiral), LiChropur™, ≥99.0%
InChI
1S/C9H9FN4O5/c1-4(9(11)15)12-6-2-5(10)7(13(16)17)3-8(6)14(18)19/h2-4,12H,1H3,(H2,11,15)/t4-/m0/s1
SMILES string
C[C@H](Nc1cc(F)c(cc1[N+]([O-])=O)[N+]([O-])=O)C(N)=O
InChI key
NEPLBHLFDJOJGP-BYPYZUCNSA-N
grade
derivatization grade (chiral)
assay
≥99.0% (sum of enantiomers, TLC)
≥99.0%
form
powder
optical activity
[α]20/D +56±2°, c = 1% in acetone
optical purity
enantiomeric ratio: ≥99.5:0.5 (HPLC)
quality
LiChropur™
technique(s)
HPLC: suitable
storage temp.
2-8°C
Quality Level
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Application
在一项使用反相高效液相色谱-电喷雾电离质谱（RPHPLC-ESI-MS）了解罕见氨基酸的研究中，FDAA被用作衍生化试剂。
General description
Nα-(2,4-二硝基-5-氟苯基)-L-丙氨酰胺（FDAA）是一种手性衍生剂（CDA），与其他CDA相比具有高对映选择性和低灵敏度。它常被用于指定痕量氨基酸的立体化学。
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Chirality determination of unusual amino acids using precolumn derivatization and liquid chromatography-electrospray ionization mass spectrometry.
Hess S
Journal of Chromatography A, 1035(2), 211-219 (2004)
Sonja Hess et al.
Analytical biochemistry, 311(1), 19-26 (2002-11-21)
Silk fibroins from moth larvae and spiders are composed of highly repetitive Ala- and Gly-rich blocks that determine their structure, properties, and function. To investigate the metabolic integration of isotopically labeled amino acids in the excreted silk, the enrichment of
Michael J Berna et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 846(1-2), 359-363 (2006-09-12)
The ability to selectively measure serine enantiomer concentrations in rat brain microdialysate is essential during drug discovery to study the interaction of d-serine with the N-methyl-d-aspartate (NMDA) subtype of the glutamate receptor. NMDA receptor-stimulating agents, such as d-serine, have been
G Szókán et al.
Journal of chromatography, 444, 115-122 (1988-07-01)
Reversed-phase high-performance liquid chromatography and pre-column derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (Marfey's reagent) were used for monitoring racemization in peptides, amino acids and their derivatives by separation of optical isomers of amino acids. The technique was applied to the analysis of
R Bhushan et al.
Amino acids, 36(3), 571-579 (2008-07-10)
Some non-protein alpha-amino acids were derivatized with 1-fluoro-2,4-dinitrophenyl-5-L-alaninamide (Marfey's reagent, MR, FDNP-L-Ala-NH(2),) and four of its structural variants FDNP-L-Phe-NH(2), FDNP-L-Val-NH(2), FDNP-L-Leu-NH(2) and FDNP-L-Pro-NH(2). The resultant diastereomers were separated by normal and reversed phase thin layer chromatography (TLC) and reversed phase
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