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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
Beilstein:
6820069
MDL编号:
UNSPSC代码:
23151816
PubChem化学物质编号:
NACRES:
NA.22
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等级

derivatization grade (chiral)

质量水平

方案

≥99.0% (sum of enantiomers, TLC)
≥99.0%

表单

powder

旋光性

[α]20/D +56±2°, c = 1% in acetone

光学纯度

enantiomeric ratio: ≥99.5:0.5 (HPLC)

质量

LiChropur

技术

HPLC: suitable

储存温度

2-8°C

SMILES字符串

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

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一般描述

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。

应用

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。

其他说明

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

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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)
D R Goodlett et al.
Journal of chromatography. A, 707(2), 233-244 (1995-07-21)
A high-performance liquid chromatography-electrospray ionization-mass spectrometric (LC-ESI-MS) method is presented that allows rapid and accurate determination of amino acid chiral purity in a peptide. Peptides are hydrolyzed in hydrochloric acid-d1/acetic acid-d4 and then converted to diastereomers by derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-alanine
Evan W Rogers et al.
Journal of natural products, 68(6), 891-896 (2005-06-25)
The absolute configurations of fistularin-3, 11-epi-fistularin-3, and a related bis-oxazolidinone were determined by microscale hydrolysis followed by derivatization with 1-fluoro-2,4-dinitrophenyl-5-l-alaninamide. Samples of fistularin-3 from Verongid marine sponges collected in the Great Barrier Reef (Australia), Baía de Todos os Santos (Brazil)
D B Goodnough et al.
Journal of chromatography. B, Biomedical applications, 672(2), 290-294 (1995-10-20)
D-Serine has recently been described to be present in the brain at high concentrations. However, while prior research has demonstrated that L-phosphoserine is the major precursor of L-serine in the brain, the possible role of D-phosphoserine as the direct precursor
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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