D7906
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide
chiral derivatizing agent , powder
동의어(들):
FDAA, Marfey’s reagent
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C9H9FN4O5
CAS 번호:
Molecular Weight:
272.19
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.25
Beilstein/REAXYS Number:
6820069
MDL number:
Form:
powder
제품 이름
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide, powder
InChI key
NEPLBHLFDJOJGP-BYPYZUCNSA-N
SMILES string
C[C@H](Nc1cc(F)c(cc1[N+]([O-])=O)[N+]([O-])=O)C(N)=O
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
form
powder
storage temp.
2-8°C
Quality Level
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관련 카테고리
Application
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.
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
저장 등급
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
C3 and 2D C3 Marfey?s methods for amino acid analysis in natural products
Vijayasarathy S, et al.
Journal of Natural Products, 79(2), 421-427 (2016)
High concentrations of D-amino acids in human gastric juice
Nagata Y, et al.
Amino Acids, 32(1), 137-140 (2007)
The functional dlt operon of Clostridium butyricum controls the D-alanylation of cell wall components and influences cell septation and vancomycin-induced lysis
Wydau-Dematteis S, et al.
Anaerobe, 35, 105-114 (2015)
Purification of branched-chain amino acid aminotransferase from Helicobacter pylori NCTC 11637
Saito M, et al.
Amino Acids, 33(3), 445-449 (2007)
A comparison of the direct and indirect LC methods for separating enantiomers of unusual glycine and alanine amino acid analogues
Peter A, et al.
Chromatographia, 56(1), S79-S89 (2002)
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