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O-Phosphorylethanolamine

CAS# 1071-23-4

O-Phosphorylethanolamine

Catalog No. BCN1759----Order now to get a substantial discount!

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O-Phosphorylethanolamine: 5mg $6 In Stock
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Quality Control of O-Phosphorylethanolamine

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Chemical structure

O-Phosphorylethanolamine

3D structure

Chemical Properties of O-Phosphorylethanolamine

Cas No. 1071-23-4 SDF Download SDF
PubChem ID 1015 Appearance Powder
Formula C2H8NO4P M.Wt 141.1
Type of Compound Miscellaneous Storage Desiccate at -20°C
Synonyms 2-Aminoethyl dihydrogen phosphate
Solubility H2O : 250 mg/mL (1772.30 mM; Need ultrasonic)
Chemical Name 2-AMINOETHYL DIHYDROGEN PHOSPHATE
SMILES NCCO[P](O)(O)=O
Standard InChIKey SUHOOTKUPISOBE-UHFFFAOYSA-N
Standard InChI InChI=1S/C2H8NO4P/c3-1-2-7-8(4,5)6/h1-3H2,(H2,4,5,6)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of O-Phosphorylethanolamine

The Proteus mirabilis

Biological Activity of O-Phosphorylethanolamine

Description1. O-Phosphorylethanolamine coupled with aminosilanized nanodiamonds show a homogeneous interaction with the titanium substrate.

O-Phosphorylethanolamine Dilution Calculator

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O-Phosphorylethanolamine Molarity Calculator

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Preparing Stock Solutions of O-Phosphorylethanolamine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 7.0872 mL 35.4359 mL 70.8717 mL 141.7434 mL 177.1793 mL
5 mM 1.4174 mL 7.0872 mL 14.1743 mL 28.3487 mL 35.4359 mL
10 mM 0.7087 mL 3.5436 mL 7.0872 mL 14.1743 mL 17.7179 mL
50 mM 0.1417 mL 0.7087 mL 1.4174 mL 2.8349 mL 3.5436 mL
100 mM 0.0709 mL 0.3544 mL 0.7087 mL 1.4174 mL 1.7718 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on O-Phosphorylethanolamine

Detonation nanodiamonds biofunctionalization and immobilization to titanium alloy surfaces as first steps towards medical application.[Pubmed:25550742]

Beilstein J Org Chem. 2014 Nov 26;10:2765-2773.

Due to their outstanding properties nanodiamonds are a promising nanoscale material in various applications such as microelectronics, polishing, optical monitoring, medicine and biotechnology. Beyond the typical diamond characteristics like extreme hardness or high thermal conductivity, they have additional benefits as intrinsic fluorescence due to lattice defects without photobleaching, obtained during the high pressure high temperature process. Further the carbon surface and its various functional groups in consequence of the synthesis, facilitate additional chemical and biological modification. In this work we present our recent results on chemical modification of the nanodiamond surface with phosphate groups and their electrochemically assisted immobilization on titanium-based materials to increase adhesion at biomaterial surfaces. The starting material is detonation nanodiamond, which exhibits a heterogeneous surface due to the functional groups resulting from the nitrogen-rich explosives and the subsequent purification steps after detonation synthesis. Nanodiamond surfaces are chemically homogenized before proceeding with further functionalization. Suspensions of resulting surface-modified nanodiamonds are applied to the titanium alloy surfaces and the nanodiamonds subsequently fixed by electrochemical immobilization. Titanium and its alloys have been widely used in bone and dental implants for being a metal that is biocompatible with body tissues and able to bind with adjacent bone during healing. In order to improve titanium material properties towards biomedical applications the authors aim to increase adhesion to bone material by incorporating nanodiamonds into the implant surface, namely the anodically grown titanium dioxide layer. Differently functionalized nanodiamonds are characterized by infrared spectroscopy and the modified titanium alloys surfaces by scanning and transmission electron microscopy. The process described shows an adsorption and immobilization of modified nanodiamonds on titanium; where aminosilanized nanodiamonds coupled with O-Phosphorylethanolamine show a homogeneous interaction with the titanium substrate.

Description

Phosphorylethanolamine is an endogenous metabolite.

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