Z-Glu-OH

CAS# 1155-62-0

Z-Glu-OH

Catalog No. BCC2781----Order now to get a substantial discount!

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Chemical structure

Z-Glu-OH

3D structure

Chemical Properties of Z-Glu-OH

Cas No. 1155-62-0 SDF Download SDF
PubChem ID 70866 Appearance Powder
Formula C13H15NO6 M.Wt 281.3
Type of Compound N/A Storage Desiccate at -20°C
Synonyms N-Cbz-L-Glutamic Acid;N-Benzyloxycarbonyl-L-Glutamic Acid
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2S)-2-(phenylmethoxycarbonylamino)pentanedioic acid
SMILES C1=CC=C(C=C1)COC(=O)NC(CCC(=O)O)C(=O)O
Standard InChIKey PVFCXMDXBIEMQG-JTQLQIEISA-N
Standard InChI InChI=1S/C13H15NO6/c15-11(16)7-6-10(12(17)18)14-13(19)20-8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,14,19)(H,15,16)(H,17,18)/t10-/m0/s1
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.

Z-Glu-OH Dilution Calculator

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Z-Glu-OH Molarity Calculator

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Preparing Stock Solutions of Z-Glu-OH

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.5549 mL 17.7746 mL 35.5492 mL 71.0985 mL 88.8731 mL
5 mM 0.711 mL 3.5549 mL 7.1098 mL 14.2197 mL 17.7746 mL
10 mM 0.3555 mL 1.7775 mL 3.5549 mL 7.1098 mL 8.8873 mL
50 mM 0.0711 mL 0.3555 mL 0.711 mL 1.422 mL 1.7775 mL
100 mM 0.0355 mL 0.1777 mL 0.3555 mL 0.711 mL 0.8887 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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Background on Z-Glu-OH

Z-Glu-OH

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References on Z-Glu-OH

Conformational study of Z-Glu-OH and Z-Arg-OH: dispersion interactions versus conventional hydrogen bonding.[Pubmed:23095122]

J Phys Chem A. 2013 Feb 14;117(6):1216-27.

The gas-phase conformational preferences of the model dipeptides Z-Glu-OH and Z-Arg-OH have been studied in the low-temperature environment of a supersonic jet. IR-UV ion-dip spectra obtained using the free electron laser FELIX provide conformation-specific IR spectra, which in combination with density functional theory (DFT) allow us to determine the conformational structures of the peptides. Molecular dynamics modeling using simulated annealing generates a variety of low-energy structures, for which geometry optimization and frequency calculations are then performed using the B3LYP functional with the 6-311+G(d,p) basis set. By comparing experimental and theoretical IR spectra, three conformations for Z-Glu-OH and two for Z-Arg-OH have been identified. For three of the five structures, the dispersion interaction provides an important contribution to the stabilization, emphasizing the importance of these forces in small peptides. Therefore, dispersion-corrected DFT functionals (M05-2X and B97D) have also been employed in our theoretical analysis. Second-order Moller-Plesset perturbation theory (MP2) has been used as benchmark for the relative energies of the different conformational structures. Finally, we address the ongoing debate on the gas-phase structure of arginine by elucidating whether isolated arginine is canonical, tautomeric, or zwitterionic.

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