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Merck
CN

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
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grade

derivatization grade (chiral)

Quality Level

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

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

InChI key

NEPLBHLFDJOJGP-BYPYZUCNSA-N

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。

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。

Other Notes

探索最适于 HPLCLC-MS分析的LiChropur试剂
检测非常规手性 α-氨基酸类似物的衍生化试剂

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


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pictograms

Exclamation mark

signalword

Warning

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
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



全球贸易项目编号

货号GTIN
71478-50MG04061832848716