71478
Nα-(2,4-ジニトロ-5-フルオロフェニル)-L-アラニンアミド
derivatization grade (chiral), LiChropur™, ≥99.0%
別名:
FDAA, Marfey試薬
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この商品について
実験式（ヒル表記法）:
C9H9FN4O5
CAS番号:
分子量:
272.19
UNSPSC Code:
23151816
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6820069
製品名
Nα-(2,4-ジニトロ-5-フルオロフェニル)-L-アラニンアミド, 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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関連するカテゴリー
Application
FDAAは、逆相高速液体クロマトグラフィー電子スプレーイオン化質量分析（RPHPLC-ESI-MS）を用いて行われた、まれなアミノ酸を理解するための研究で誘導化試薬として使用されました。
General description
Nα-(2,4-ジニトロ-5-フルオロフェニル)-L-アラニンアミド（FDAA）は、他のCDAと比較してエナンチオ選択性が高く、感受性は低いキラル誘導体化剤（CDA）です。アミノ酸の立体化学を極微量で特定するのに広く使用されています。
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
保管分類
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)
R Bhushan et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(29), 3148-3161 (2011-07-09)
The present paper describes an updated knowledge and status on Marfey's reagent (MR), 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (FDNP-L-Ala-NH(2)). The reagent is used for pre-column derivatization of amino acids followed by HPLC separation of the diastereomers so formed. Emphasis is put on the
J G Adamson et al.
Analytical biochemistry, 202(1), 210-214 (1992-04-01)
A chromatographic assay has been developed to quantitate racemization occurring during attachment of protected amino acids to peptide synthesis resins. Acidolytic cleavage of deprotected amino acids from supports and subsequent derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (Marfey's reagent) gave diastereomers separable by
S Kochhar et al.
Analytical biochemistry, 178(1), 17-21 (1989-04-01)
Amino acids are quantitatively determined by precolumn derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide and reversed-phase high-performance liquid chromatography with photometric detection at 340 nm. Excellent chromatographic resolution of a mixture of the derivatives of 20 amino acids including proline and cystine is
A D Tran et al.
Journal of chromatography, 516(1), 241-249 (1990-09-07)
Separation of amino acid enantiomers and peptide isomers has been made possible through the use of Marfey's reagent and high-performance capillary electrophoresis (HPCE). Samples of amino acids and peptides were first derivatized with Marfey's reagent and subsequently analyzed by HPCE.
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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