TribenzylamineCAS# 620-40-6 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 620-40-6 | SDF | Download SDF |
| PubChem ID | 24321 | Appearance | Powder |
| Formula | C21H21N | M.Wt | 287.4 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | N,N-dibenzyl-1-phenylmethanamine | ||
| SMILES | C1=CC=C(C=C1)CN(CC2=CC=CC=C2)CC3=CC=CC=C3 | ||
| Standard InChIKey | MXHTZQSKTCCMFG-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C21H21N/c1-4-10-19(11-5-1)16-22(17-20-12-6-2-7-13-20)18-21-14-8-3-9-15-21/h1-15H,16-18H2 | ||
| 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. |
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| 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. |
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| 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. | ||
| Targets | Estrogen receptor | Progestogen receptor |
Tribenzylamine Dilution Calculator
Tribenzylamine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.4795 mL | 17.3974 mL | 34.7947 mL | 69.5894 mL | 86.9868 mL |
| 5 mM | 0.6959 mL | 3.4795 mL | 6.9589 mL | 13.9179 mL | 17.3974 mL |
| 10 mM | 0.3479 mL | 1.7397 mL | 3.4795 mL | 6.9589 mL | 8.6987 mL |
| 50 mM | 0.0696 mL | 0.3479 mL | 0.6959 mL | 1.3918 mL | 1.7397 mL |
| 100 mM | 0.0348 mL | 0.174 mL | 0.3479 mL | 0.6959 mL | 0.8699 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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Tribenzylamine C-H activation and intermolecular hydrogen transfer promoted by WCl6.[Pubmed:24624963]
Inorg Chem. 2014 Apr 7;53(7):3832-8.
The 1:1 molar reaction of WCl6 with Tribenzylamine (tba), in dichloromethane, selectively afforded the iminium salt [(PhCH2)2N horizontal lineCHPh][WCl6], 1, and the ammonium one [tbaH][WCl6], 2, in equimolar amounts. The products were fully characterized by means of spectroscopic methods, analytical methods, and X-ray diffractometry. Density functional theory calculations were carried out with the aim of comprehending the mechanistic aspects.
Multiple hindered rotators in a gyroscope-inspired tribenzylamine hemicryptophane.[Pubmed:21271707]
J Org Chem. 2011 Mar 4;76(5):1418-24.
A gyroscope-inspired Tribenzylamine hemicryptophane provides a vehicle for exploring the structure and properties of multiple p-phenylene rotators within one molecule. The hemicryptophane was synthesized in three steps in good overall yield using mild conditions. Three rotator-forming linkers were cyclized to form a rigid cyclotriveratrylene (CTV) stator framework, which was then closed with an amine. The gyroscope-like molecule was characterized by (1)H NMR and (13)C NMR spectroscopy, and the structure was solved by X-ray crystallography. The rigidity of the two-component CTV-trismethylamine stator was investigated by (1)H variable-temperature (VT) NMR experiments and molecular dynamics simulations. These techniques identified gyration of the three p-phenylene rotators on the millisecond time scale at -93 degrees C, with more dynamic but still hindered motion at room temperature (27 degrees C). The activation energy for the p-phenylene rotation was determined to be ~10 kcal mol(-1). Due to the propeller arrangement of the p-phenylenes, their rotation is hindered but not strongly correlated. The compact size, simple synthetic route, and molecular motions of this gyroscope-inspired Tribenzylamine hemicryptophane make it an attractive starting point for controlling the direction and coupling of rotators within molecular systems.
Extractive separation and determination of chromium in tannery effluents and electroplating waste water using tribenzylamine as the extractant.[Pubmed:19135302]
J Hazard Mater. 2009 Jun 15;165(1-3):886-92.
A simple extractive separation method has been developed for the determination of chromium based on the extraction of Cr (VI) as its ion-pair with Tribenzylamine (TBA). The ion-pair is extracted at acidic pH using toluene as the diluent. The concentration of chromium in the organic phase was measured spectrophotometrically at 309 nm. The influence of experimental variables such as pH, sample volume, equilibration time, diverse ions etc. has been studied in detail. The extracted chromium (VI) could be stripped to the aqueous phase using NaOH as the stripping agent. The extracts were characterized using FT-IR spectroscopy. A detection limit of 0.08 microg mL(-1) could be achieved and the validity of the method was checked in real tannery effluent, electroplating waste water and spiked water samples.
