(S)-NIFE
(Synonyms: N-(4-硝基苯氧基羰基)-L-苯基丙氨酸2-甲氧基乙酯) 目录号 : GC40621
A chiral amino acid derivatizing agent for HPLC
Cas No.:328406-65-1
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
(S)-NIFE is a chiral derivatizing agent for amino acid analysis by HPLC. It can also be used for derivatization of secondary amino acids.
| Cas No. | 328406-65-1 | SDF | |
| 别名 | N-(4-硝基苯氧基羰基)-L-苯基丙氨酸2-甲氧基乙酯 | ||
| Canonical SMILES | O=C(N[C@H](C(OCCOC)=O)CC1=CC=CC=C1)OC2=CC=C([N+]([O-])=O)C=C2 | ||
| 分子式 | C19H20N2O7 | 分子量 | 388.4 |
| 溶解度 | DMF: 20 mg/mL,DMF:PBS (pH 7.2); (1:7): 0.12 mg/mL,DMSO: 10 mg/mL,Ethanol: 3 mg/mL | 储存条件 | Store at -20°C |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.5747 mL | 12.8733 mL | 25.7467 mL |
| 5 mM | 0.5149 mL | 2.5747 mL | 5.1493 mL |
| 10 mM | 0.2575 mL | 1.2873 mL | 2.5747 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
S-modified NiFe-phosphate hierarchical hollow microspheres for efficient industrial-level seawater electrolysis
J Colloid Interface Sci 2023 Mar;633:668-678.PMID:36473357DOI:10.1016/j.jcis.2022.11.113.
For sustained hydrogen generation from seawater electrolysis, an efficient and specialized catalyst must be designed to cope with the slow anode reaction and chloride ions (Cl-) corrosion. In this work, an S-modified NiFe-phosphate with hierarchical and hollow microspheres was grown on the NiFe foam skeleton (S-NiFe-Pi/NFF), acting as a bifunctional catalyst to enable industrial-scale seawater electrolysis. The introduction of S distorted the lattice of NiFe-phosphate and regulated the local electronic environment around Ni/Fe active metal, both of which enhanced the electrocatalytic activity. Additionally, the existence of phosphate groups repelled Cl- on the surface and enhanced corrosion resistance, enabling stable long-term operation in seawater. The double-electrode electrolyzer composed of the hollow-structured S-NiFe-Pi/NFF as both cathode and anode exhibited a potential of 1.68 V at 100 mA cm-2 for seawater electrolysis. Particularly, to achieve industrial requirements of 500 mA cm-2, it only required a low cell voltage of 1.8 V and demonstrated a consistent response over 100 h, which outperformed the pair of Pt/C || IrO2. This study provides a feasible idea for the preparation of electrocatalysts that are with both highly activity and corrosion resistance, which is crucial for the implementation of industrial-scale seawater electrolysis.
Three-dimensional self-supporting catalyst with NiFe alloy/oxyhydroxide supported on high-surface cobalt hydroxide nanosheet array for overall water splitting
J Colloid Interface Sci 2022 Jan 15;606(Pt 1):873-883.PMID:34428683DOI:10.1016/j.jcis.2021.08.020.
The development of available dual-function electrocatalysts is of great significance to the effective storage of excess electricity. Here, we obtained a three-dimensional Co(OH)2 nanosheet with high surface area on nickel foam (Co(OH)2/NF) via conventional hydrothermal. NiFe-coated Co(OH)2 nanosheet array (NiFe@Co(OH)2 NSAs/NF) was further constructed by electrodeposition for water splitting. By optimizing and regulating the deposition time, NiFe@Co(OH)2 NSAs/NF with a deposition time of 500 S (NiFe-500@Co(OH)2 NSAs/NF) only needs 98 mV of overpotential and can be stabilized for 100 h for hydrogen evolution at 10 mA cm-2 due to the rich density active components for NiFe alloy/oxyhydroxide layer and interaction with Co(OH)2 nanosheets. Thanks to the excellent 3D nanosheet array structure and the close integration between Co(OH)2 and the upper layer NiFe, NiFe@Co(OH)2 NSAs/NF with a deposition time of 200 S (NiFe-200@Co(OH)2 NSAs/NF) can provide 10 mA cm-2 with only 204 mV and maintain constant catalysis within 100 h. Therefore, the constructed NiFe@Co(OH)2 NSAs/NF (500||200) double-electrode cell for water splitting requires only 1.58 V drive potential and can maintain 24 h durability at 10 mA cm-2. The design of the catalyst opens up new ideas for the large-scale application of transition metals in water splitting.
High-performance liquid chromatographic enantioseparation of (R,S)-fluoxetine using Marfey's reagent and (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as chiral derivatizing reagents along with direct thin-layer chromatographic resolution and isolation of enantiomers using L-tartaric acid as mobile phase additive
Biomed Chromatogr 2010 Nov;24(11):1152-8.PMID:20954205DOI:10.1002/bmc.1421.
Chiral assay of enantiomers of fluoxetine was achieved in pharmaceutical formulations using direct and indirect methods. L-tartaric acid was used as a mobile phase additive in thin-layer chromatography; the enantiomers were separated and isolated and were used to determine the elution order in HPLC. (R,S)-flouxetine was derivatized with (S)-N-(4-nitrophenoxycarbonyl)phenylalanine methoxyethyl ester [(S)-NIFE], Marfey's reagent and 1-fluoro-2,4-dinitrophenyl-L-methionine amide (FDNP-L-Met-NH₂. The diastereomers were separated using RP-HPLC. The effect of flow rate and TFA concentration on resolution was studied. The diastereomers obtained by derivatization with FDNP-L-Met-NH₂ were also separated by RP-TLC.
Development of an UPLC-MS/MS method for simultaneous quantitation of 11 d-amino acids in different regions of rat brain: Application to a study on the associations of d-amino acid concentration changes and Alzheimer's disease
J Chromatogr B Analyt Technol Biomed Life Sci 2017 Jul 15;1058:40-46.PMID:28531844DOI:10.1016/j.jchromb.2017.05.011.
There are significant differences in d-amino acid concentrations between healthy people and Alzheimer's disease patients. In order to investigate the potential correlation between d-amino acids and Alzheimer's disease, a simple and sensitive ultra high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method has been developed. The method was applied to simultaneous determination of 11 d-amino acids in different regions of rat brain. Rat brain homogenates were firstly pretreated with protein precipitation procedure and then derivatized with (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester [(S)-NIFE]. Baseline separation of the derivatives was achieved on an ACQUITY UPLC BEH C18 column (2.1 mm×50mm, 1.7μm). The mobile phase consisted of acetonitrile and water (containing 8mM ammonium hydrogen carbonate) and the flow rate was 0.6mLmin-1. The derived analytes were sensitively detected by multiple reaction monitoring in the positive ion mode. The lower limits of quantitation ranged from 0.06 to 10ngmL-1 with excellent linearity (r≥0.9909). The intra- and inter-day RSD were in the range of 3.6-12% and 5.7-12%, respectively. The recovery rate was 82.5%-95.3%. With this UPLC-MS/MS method, the 11 d-amino acids in hippocampus, cerebral cortex, olfactory bulb and cerebellum from Alzheimer's disease rats and age-matched controls could be simultaneously determined. Compared with the normal controls, the concentrations of d-serine, d-alanine, d-leucine, and d-proline in hippocampus and cerebral cortex of Alzheimer's disease rat brain were significantly decreased, while no differences in olfactory bulb and cerebellum of all the d-amino acids were observed. The different amounts and distribution of d-amino acids in brain between the two groups, which regulated by particular pathological changes of Alzheimer's disease, would give new insights into further study in neuropathogenesis and provide novel therapeutic targets of Alzheimer's disease.
Atomic Sulfur Filling Oxygen Vacancies Optimizes H Absorption and Boosts the Hydrogen Evolution Reaction in Alkaline Media
Angew Chem Int Ed Engl 2021 Jun 14;60(25):14117-14123.PMID:33843135DOI:10.1002/anie.202104055.
The hydrogen evolution reaction (HER) usually has sluggish kinetics in alkaline solution due to the difficulty in forming binding protons. Herein we report an electrocatalyst in which sulfur atoms are doping in the oxygen vacancies (VO ) of inverse spinel NiFe2 O4 (S-NiFe2 O4 ) to create active sites with enhanced electron transfer capability. This electrocatalyst has an ultralow overpotential of 61 mV at the current density of 10 mA cm-2 and long-term stability of 60 h at 1.0 Acm-2 in 1.0 M KOH media. In situ Raman spectroscopy revealed that S sites adsorb hydrogen adatom (H*) and in situ form S-H*, which favor the production of hydrogen and boosts HER in alkaline solution. DFT calculations further verified that S introduction lowered the energy barrier of H2 O dissociation. Both experimental and theoretical investigations confirmed S atoms are active sites of the S-NiFe2 O4 .