Home>>Signaling Pathways>> Proteases>> Endogenous Metabolite>>(2-Aminoethyl)phosphonic acid

(2-Aminoethyl)phosphonic acid Sale

(Synonyms: 2-氨基乙基膦酸) 目录号 : GC38299

2-Aminoethylphosphonic acid (2-AEP, (2-Aminoethyl)phosphonic acid) is a type of abundant and ubiquitous naturally occurring phosphonate used as sources of phosphorus by many prokaryotic lineages.

(2-Aminoethyl)phosphonic acid Chemical Structure

Cas No.:2041-14-7

规格 价格 库存 购买数量
100mg
¥450.00
现货
200mg 待询 待询
500mg 待询 待询

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

View current batch:

产品描述

2-Aminoethylphosphonic acid (2-AEP, (2-Aminoethyl)phosphonic acid) is a type of abundant and ubiquitous naturally occurring phosphonate used as sources of phosphorus by many prokaryotic lineages.

[1] Shu Wang, et al. J Chromatogr A. 2018 Oct 12;1571:147-154.

Chemical Properties

Cas No. 2041-14-7 SDF
别名 2-氨基乙基膦酸
Canonical SMILES NCCP(O)(O)=O
分子式 C2H8NO3P 分子量 125.06
溶解度 Soluble in DMSO 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。
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。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 7.9962 mL 39.9808 mL 79.9616 mL
5 mM 1.5992 mL 7.9962 mL 15.9923 mL
10 mM 0.7996 mL 3.9981 mL 7.9962 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

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
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

Research Update

Phosphonic acid-functionalized poly(amido amine) macromers for biomedical applications

J Biomed Mater Res A 2020 Oct;108(10):2100-2110.PMID:32319210DOI:10.1002/jbm.a.36969.

Novel phosphonic acid-functionalized poly(amido amine) (PAA) macromers are synthesized through aza-Michael addition of 2-Aminoethyl phosphonic acid or its mixture with 5-amino-1-pentanol at different ratios onto N,N'-methylene bis(acrylamide) to control the amount of phosphonic acid functionality. The macromers were homo- and copolymerized with 2-hydroxyethyl methacrylate at different ratios to obtain hydrogels with various hydrophilicities. The hydrogels' swelling, biodegradation and mineralization properties were evaluated. The swelling and degradation rates of the gels can be tuned by the chemical structure of PAA macromer precursors as well as pH and CaCl2 pre-treatment. The hydrogels show composition-dependent mineralization in SBF and 5xSBF, as evidenced from Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX) analyses. The degradation products of the hydrogels have no effect on U-2 OS, Saos-2 and NIH 3T3 cells, suggesting their cytocompatibility. Overall, these materials have potential to be used as nontoxic degradable biomaterials.

Amino-Functionalized Layered Crystalline Zirconium Phosphonates: Synthesis, Crystal Structure, and Spectroscopic Characterization

Inorg Chem 2016 Jun 20;55(12):6278-85.PMID:27254781DOI:10.1021/acs.inorgchem.6b00943.

Two new layered zirconium phosphonates functionalized with amino groups were synthesized starting from aminomethylphosphonic acid in the presence of different mineralizers, and their structures were solved from powder X-ray diffraction data. Their topologies are unprecedented in zirconium phosphonate chemistry: the first, of formula ZrH[F3(O3PCH2NH2)], prepared in the presence of hydrofluoric acid, features uncommon ZrO2F4 units and a remarkable thermal stability; the second, of formula Zr2H2[(C2O4)3(O3PCH2NH2)2]·2H2O, prepared in the presence of oxalic acid, is based on ZrO7 units with oxalate anions coordinated to the metal atom, which were never observed before in any zirconium phosphonate. In addition, the structure of another compound based on (2-Aminoethyl)phosphonic acid is reported, which was the object of a previously published study. This compound has layered α-type structure with -NH3(+) groups located in the interlayer space. All of the reported compounds were further characterized by means of vibrational spectroscopy, which provided important information on fine structural details that cannot be deduced from the powder X-ray diffraction data.

Efficacy of varying the NMEP concentrations in the NMGly-NMEP self-etching primer on the resin-tooth bonding

Biomaterials 2005 May;26(15):2653-61.PMID:15585268DOI:10.1016/j.biomaterials.2004.07.039.

It is well understood that the application of a self-etching primer enhances the bonding at the resin-teeth interface. In this study, we designed a self-etching primer consisting of N-methacryloyl glycine (NMGly) and N-methacryloyl-2-aminoethyl phosphonic acid (NMEP). The demineralization effects on the hydroxyapatite or dentin by the carboxylic acid in the NMGly and by the phosphonic acid in the NMEP and their effects on the bond strength of the resin to the tooth were examined. The application of the NMGly-NMEP solution to the enamel resulted in an increase in the bond strength when additional amounts of NMEP were added to the NMGly aqueous solution. This increase was due to the phosphonic acid in the NMEP demineralizing the enamel. Conversely, the addition of the NMEP to the NMGly solution resulted in a decrease in the bond strength to the dentin. The optimal concentration of the NMEP in the NMGly-NMEP solution resulted in bond strengths of over 20 MPa for both the enamel and dentin.

Protein binding to amphoteric polymer brushes grafted onto a porous hollow-fiber membrane

Biotechnol Prog 2007 Nov-Dec;23(6):1425-30.PMID:17918859DOI:10.1021/bp070264q.

Three kinds of ampholites, i.e., 3-aminopropionic acid (NH2C2H4COOH), (2-Aminoethyl)phosphonic acid (NH2C2H4PO3H2), and 2-aminoethane-1-sulfonic acid (NH2C2H4SO3H), were introduced into an epoxy group-containing polymer brush grafted onto a porous hollow-fiber membrane with a porosity of 70% and pore size of 0.36 microm. The amphoteric group density of the hollow-fiber ranged from 0.50 to 0.72 mmol/g. Three kinds of proteins, i.e., lactoferrin (Lf), cytochrome c (Cyt c), and lysozyme (Ly), were captured by the amphoteric polymer brush during the permeation of the protein solution across the ampholite-immobilized porous hollow-fiber membrane. Multilayer binding of the protein to the amphoteric polymer brush, with a degree of multilayer binding of 3.3, 8.6, and 15 for Lf, Cyt c, and Ly, respectively, with the (2-aminoethyl)phosphonic acid-immobilized porous hollow-fiber membrane, was demonstrated with a negligible diffusional mass-transfer resistance of the protein to the ampholite immobilized. The 2-aminoethane-1-sulfonic acid-immobilized porous hollow-fiber membrane exhibited the lowest initial flux of the protein solution, 0.41 m/h at a transmembrane pressure of 0.1 MPa and 298 K, and the highest equilibrium binding capacity of the protein, e.g., 130 mg/g for lysozyme. Extension and shrinkage of the amphoteric polymer brushes were observed during the binding and elution of the proteins.

[Utilization and growth response of Chrysosporum ovalisporum to different phosphorus compounds]

Ying Yong Sheng Tai Xue Bao 2019 Dec;30(12):4277-4285.PMID:31840474DOI:10.13287/j.1001-9332.2019120.038.

To explore the ability of bloom-forming cyanobacterium Chrysosporum ovalisporum to utilize different kinds of phosphorus compounds in the water column, we examined the growth response of C. ovalisporum in the laboratory by taking dipotassium hydrogen phosphate as the control and set different treatments of phosphorus substrates. The results showed that C. ovalisporum could utilize sodium tripolyphosphate and terasodium pyrophosphate decahydrate, with better utilization of sodium tripolyphosphate. After 15 days, it had the highest biomass and chlorophyll a concentrations under the treatment of sodium tripolyphosphate, with a value of (426.96±47.42) mg·L-1 and (1852.34±116.60) μg·L-1, respectively. Compared with the control, there was no significant difference in biomass of C. ovalisporum under both the (2-Aminoethyl)-phosphonic acid and disodium β-glycerol phosphate pentahydrate treatments. The change characteristics of dissolved inorganic phosphate were related to the alkaline phosphatase activity, indicating that C. ovalisporum was able to utilize these two organophosphorus compounds via enzyme hydrolysis. The concentration of dissolved inorganic phosphate reached 0 mg·L-1 during the whole experiment when the C. ovalisporum were fed with glyphosate. Biomass, specific growth rate, chlorophyll a concentration and photosynthetic activity of algal cells were significantly lower than those of the control, indicating that C. ova-lisporum could not uptake phosphorus compounds in the glyphosate substrate and thus their growth being inhibited. Our results present new insights to understand the diffusion mechanism of C. ovalisporum into different aquatic ecosystems and had theoretical reference value for the prevention and control of new cyanobacterial blooms.