Tribenzylamine | CAS#620-40-6 | biochemical

MedKoo Cat#: 591755 | Name: Tribenzylamine

Featured

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Tribenzylamine is an organic tertiary amine featuring a central nitrogen atom bonded to three benzyl groups, imparting hydrophobic and steric properties. Its structural framework enhances its utility as a precursor or intermediate in organic synthesis, particularly in the production of pharmaceuticals and specialty chemicals. With moderate basicity and solubility in organic solvents, tribenzylamine is also explored for its role in coordination chemistry and catalysis.

Chemical Structure

Tribenzylamine

CAS#620-40-6

Theoretical Analysis

MedKoo Cat#: 591755

Name: Tribenzylamine

CAS#: 620-40-6

Chemical Formula: C21H21N

Exact Mass: 287.1674

Molecular Weight: 287.41

Elemental Analysis: C, 87.76; H, 7.37; N, 4.87

Price and Availability

Size	Price	Availability
5g	USD 350.00	2 Weeks
25g	USD 450.00	2 Weeks
100g	USD 650.00	2 Weeks

Bulk Inquiry

Buy Now

Add to Cart

Related CAS #

No Data

Synonym

Tribenzylamine; AI3-01809; AI3 01809; AI301809

IUPAC/Chemical Name

Tribenzylamine

InChi Key

MXHTZQSKTCCMFG-UHFFFAOYSA-N

InChi Code

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

SMILES Code

N(CC1=CC=CC=C1)(CC2=CC=CC=C2)CC3=CC=CC=C3

Appearance

TBD

Purity

>98% (or refer to the Certificate of Analysis)

Shipping Condition

Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition

Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility

Soluble in DMSO

Shelf Life

>3 years if stored properly

Drug Formulation

This drug may be formulated in DMSO

Stock Solution Storage

0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code

2934.99.03.00

More Info

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 287.41 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Concentration / Solvent Volume / Mass	1 mg	5 mg	10 mg
1 mM	1.15 mL	5.76 mL	11.51 mL
5 mM	0.23 mL	1.15 mL	2.3 mL
10 mM	0.12 mL	0.58 mL	1.15 mL
50 mM	0.02 mL	0.12 mL	0.23 mL

1: Mikata Y, Nodomi Y, Ohnishi R, Kizu A, Konno H. Tris(8-methoxy-2-quinolylmethyl)amine (8-MeOTQA) as a highly fluorescent Zn(2+) probe prepared by convenient C3-symmetric tripodal amine synthesis. Dalton Trans. 2015 May 7;44(17):8021-30. doi: 10.1039/c5dt00514k. PubMed PMID: 25827829. 2: Bortoluzzi M, Marchetti F, Pampaloni G, Zacchini S. Tribenzylamine C-H activation and intermolecular hydrogen transfer promoted by WCl6. Inorg Chem. 2014 Apr 7;53(7):3832-8. doi: 10.1021/ic5001683. Epub 2014 Mar 13. PubMed PMID: 24624963. 3: Lang X, Ma W, Zhao Y, Chen C, Ji H, Zhao J. Visible-light-induced selective photocatalytic aerobic oxidation of amines into imines on TiO2. Chemistry. 2012 Feb 27;18(9):2624-31. doi: 10.1002/chem.201102779. Epub 2012 Jan 23. PubMed PMID: 22271403. 4: Khan NS, Perez-Aguilar JM, Kaufmann T, Hill PA, Taratula O, Lee OS, Carroll PJ, Saven JG, Dmochowski IJ. Multiple hindered rotators in a gyroscope-inspired tribenzylamine hemicryptophane. J Org Chem. 2011 Mar 4;76(5):1418-24. doi: 10.1021/jo102480s. Epub 2011 Jan 27. PubMed PMID: 21271707; PubMed Central PMCID: PMC3045655. 5: Alajarin M, Orenes RA, Steed JW, Pastor A. Self-assembly of tris(ureidobenzyl)amines: flexible bricks for robust architectures. Chem Commun (Camb). 2010 Mar 7;46(9):1394-403. doi: 10.1039/b922531e. Epub 2010 Jan 27. PubMed PMID: 20162128. 6: Kalidhasan S, Ganesh M, Sricharan S, Rajesh N. Extractive separation and determination of chromium in tannery effluents and electroplating waste water using tribenzylamine as the extractant. J Hazard Mater. 2009 Jun 15;165(1-3):886-92. doi: 10.1016/j.jhazmat.2008.10.122. Epub 2008 Nov 7. PubMed PMID: 19135302. 7: Bialecki J, Ruzicka J, Attygalle AB. An unprecedented rearrangement in collision-induced mass spectrometric fragmentation of protonated benzylamines. J Mass Spectrom. 2006 Sep;41(9):1195-204. PubMed PMID: 16924596. 8: Rajesh N, Subramanian MS. A study of the extraction behavior of thallium with tribenzylamine as the extractant. J Hazard Mater. 2006 Jul 31;135(1-3):74-7. Epub 2005 Dec 15. PubMed PMID: 16359783. 9: Han WS, Chung KC, Kim MH, Ko HB, Lee YH, Hong TK. A hydrogen ion-selective poly(aniline) solid contact electrode based on dibenzylpyrenemethylamine ionophore for highly acidic solutions. Anal Sci. 2004 Oct;20(10):1419-22. PubMed PMID: 15524194. 10: Qu Y, Ding ZH, Liu JK. The first occurrence in nature of two compounds from hops. Z Naturforsch C. 2003 Sep-Oct;58(9-10):640-2. PubMed PMID: 14577623. 11: Han WS, Yoo SJ, Kim SH, Hong TK, Chung KC. Behavior of a polypyrrole solid contact pH-selective electrode based on tertiary amine ionophores containing different alkyl chain lengths between nitrogen and a phenyl group. Anal Sci. 2003 Mar;19(3):357-60. PubMed PMID: 12675339. 12: Alajarín M, Pastor A, Orenes RA, Steed JW. Dimeric self-assembling capsules derived from the highly flexible tribenzylamine skeleton. J Org Chem. 2002 Oct 4;67(20):7091-5. PubMed PMID: 12354004. 13: Jin S, Zhou R, Scheuer EM, Adamchuk J, Rayburn LL, DiSalvo FJ. Synthesis, characterization, and ligand exchange studies of W(6)S(8)L(6) cluster compounds. Inorg Chem. 2001 Jun 4;40(12):2666-74. PubMed PMID: 11375677. 14: Alberti A, Benaglia M, Macciantelli D. Mechanistic studies of radical-based processes. Use and misuse of EPR spectroscopy. Org Lett. 2000 Jun 1;2(11):1553-5. PubMed PMID: 10841477. 15: Arya SP, Malla JL, Slathia V. A selective spectrophotometric method for determination of copper with ferron. Talanta. 1987 Feb;34(2):293-5. PubMed PMID: 18964299. 16: Donaldson EM. Improved tribenzylamine-silver bromide extraction/atomic-absorption spectrophotometric method for the determination of silver in ores, related materials and zinc process solutions. Talanta. 1984 Jun;31(6):443-8. PubMed PMID: 18963626. 17: Donaldson EM, Mark E, Leaver ME. Comparison of silver results for canadian reference ores and concentrates and zinc-processing products by acid decomposition, tribenzylamine/chloroform extraction and fire-assay combined with atomic-absorption spectrophotometry. Talanta. 1984 Jan;31(1):89-96. PubMed PMID: 18963534. 18: Loeppky RN, Tomasik W, Millard TG. Ester-mediated nitrosamine formation from nitrite and secondary or tertiary amines. IARC Sci Publ. 1984;(57):353-63. PubMed PMID: 6533026. 19: Donaldson EM. Determination of silver in ores, concentrates, zinc process solutions, copper metal and copper-base alloys by atomic-absorption spectrophotometry after separation by extraction of the tribenzylamine-silver bromide complex. Talanta. 1982 Dec;29(12):1069-75. PubMed PMID: 18963258. 20: Sakakibara H, Okekawa O, Fujiwara T, Otani M, Omura S. Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3"-O-propionylleucomycin A5 (TMS-19-Q). J Antibiot (Tokyo). 1981 Aug;34(8):1001-10. PubMed PMID: 7319915.

View History

Tributylamine