Home >> Research Area >>Natural Products>>Alkaloids>> Tribenzylamine

Tribenzylamine

CAS# 620-40-6

Tribenzylamine

Catalog No. BCN1817----Order now to get a substantial discount!

Product Name & Size Price Stock
Tribenzylamine: 5mg Please Inquire In Stock
Tribenzylamine: 10mg Please Inquire In Stock
Tribenzylamine: 20mg Please Inquire Please Inquire
Tribenzylamine: 50mg Please Inquire Please Inquire
Tribenzylamine: 100mg Please Inquire Please Inquire
Tribenzylamine: 200mg Please Inquire Please Inquire
Tribenzylamine: 500mg Please Inquire Please Inquire
Tribenzylamine: 1000mg Please Inquire Please Inquire

Quality Control of Tribenzylamine

Number of papers citing our products

Chemical structure

Tribenzylamine

3D structure

Chemical Properties of Tribenzylamine

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.
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 Tribenzylamine

The herbs of Humulus lupulus

Biological Activity of Tribenzylamine

TargetsEstrogen receptor | Progestogen receptor

Tribenzylamine Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

Tribenzylamine Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Tribenzylamine

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.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

University of Maryland School of Medicine

University of Illinois at Chicago

The Ohio State University

University of Zurich

Harvard University

Colorado State University

Auburn University

Yale University

Worcester Polytechnic Institute

Washington State University

Stanford University

University of Leipzig

Universidade da Beira Interior

The Institute of Cancer Research

Heidelberg University

University of Amsterdam

University of Auckland
TsingHua University
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on Tribenzylamine

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.

Keywords:

Tribenzylamine,620-40-6,Natural Products, buy Tribenzylamine , Tribenzylamine supplier , purchase Tribenzylamine , Tribenzylamine cost , Tribenzylamine manufacturer , order Tribenzylamine , high purity Tribenzylamine

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: