TPTU

CAS# 125700-71-2

TPTU

2D Structure

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3D structure

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TPTU

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Chemical Properties of TPTU

Cas No. 125700-71-2 SDF Download SDF
PubChem ID 2733205 Appearance Powder
Formula C10H16BF4N3O2 M.Wt 297.06
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in water or 1% acetic acid
Chemical Name [dimethylamino-(2-oxopyridin-1-yl)oxymethylidene]-dimethylazanium
SMILES CN(C)C(=[N+](C)C)ON1C=CC=CC1=O
Standard InChIKey VPMAWWKDEFLLBU-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H16N3O2/c1-11(2)10(12(3)4)15-13-8-6-5-7-9(13)14/h5-8H,1-4H3/q+1
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.

TPTU Dilution Calculator

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TPTU Molarity Calculator

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Preparing Stock Solutions of TPTU

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.3663 mL 16.8316 mL 33.6632 mL 67.3265 mL 84.1581 mL
5 mM 0.6733 mL 3.3663 mL 6.7326 mL 13.4653 mL 16.8316 mL
10 mM 0.3366 mL 1.6832 mL 3.3663 mL 6.7326 mL 8.4158 mL
50 mM 0.0673 mL 0.3366 mL 0.6733 mL 1.3465 mL 1.6832 mL
100 mM 0.0337 mL 0.1683 mL 0.3366 mL 0.6733 mL 0.8416 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 TPTU

PVC membrane based potentiometric sensors for uranium determination.[Pubmed:18968336]

Talanta. 2001 Jul 6;54(6):1153-61.

Two novel uranyl PVC matrix membrane sensors responsive to uranyl ion are described. The first sensor incorporates tris(2-ethylhexyl)phosphate (TEHP) as both electroactive material and plasticizer and sodium tetraphenylborate (NaTPB) as an ion discriminator. The sensor displays a rapid and linear response for UO(2)(2+) ions over the concentration range 1x10(-1)-2x10(-5) mol l(-1) UO(2)(2+) with a cationic slope of 25.0+/-0.2 mV decade(-1). The working pH range is 2.8-3.6 and the life span is 4 weeks. The second sensor contains O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-bis(tetra-methylene)uronium hexafluorophosphate (TPTU) as a sensing material, sodium tetraphenylborate as an ion discriminator and dioctyl phenylphosphonate (DOPP) as a plasticizer. Linear and stable response for 1x10(-1)-5x10(-5) mol l(-1) UO(2)(2+) with near-Nernstian slope of 27.5+/-0.2 mV decade(-1) are obtained. The working pH range is 2.5-3.5 and the life span of the sensor is 6 weeks. Interference from many inorganic cations is negligible for both sensors. However, interference caused by some ions (e.g. Th(4+), Cu(2+), Fe(3+)) is eliminated by a prior ion exchange or solvent extraction step. Direct potentiometric determination of as little as 5 mug ml(-1) uranium in aqueous solutions shows an average recovery of 97.2+/-1.3%. Application for the determination of uranium at levels of 0.01-1 wt.% in naturally occurring and certified ores gives results with good correlation with data obtained by X-ray fluorescence.

Synthesis and biological evaluation of pyridin-2-one nucleosides.[Pubmed:11563103]

Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):731-3.

The synthesis of 1-(beta-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid and the 3-carboxamide as well as a short series of 3N-carboxamides, prepared by TPTU/HOBt coupling of primary amines with 1-(beta-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid, and their evaluation as anti-infective agents is described.

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