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723134

Tris(2-pyridylmethyl)amine

98%

Synonym(s):

TPA, TPMA, Tri-(2-picolyl)amine, Tripicolylamine

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About This Item

Empirical Formula (Hill Notation):
C18H18N4
CAS Number:
16858-01-8
Molecular Weight:
290.36
NACRES:
NA.23
PubChem Substance ID:
329763979
UNSPSC Code:
12162002
MDL number:
MFCD14708176
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assay

98%

form

solid

mp

85-89 °C

SMILES string

C(N(Cc1ccccn1)Cc2ccccn2)c3ccccn3

InChI

1S/C18H18N4/c1-4-10-19-16(7-1)13-22(14-17-8-2-5-11-20-17)15-18-9-3-6-12-21-18/h1-12H,13-15H2

InChI key

VGUWFGWZSVLROP-UHFFFAOYSA-N

Application

Atom Transfer Radical Polymerization (ATRP) ligand for the creation of telechelic polymers.
ATRP for Everyone: Ligands and Initiators for the Clean Synthesis of Functional Polymers

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1

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Certificates of Analysis (COA)

Lot/Batch Number
MKCN3910
MKCL7211
MKCH0701
MKCC4862
MKBZ8647V

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Protocols

Concepts and Tools for RAFT Polymerization

We present an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

Polymerizing via ATRP

Polymerization via ATRP procedures demonstrated by Prof. Dave Haddleton's research group at the University of Warwick.

Typical Procedures for Polymerizing via RAFT

We presents an article featuring procedures that describe polymerization of methyl methacrylate and vinyl acetate homopolymers and a block copolymer as performed by researchers at CSIRO.

Articles

ATRP Ligands & Initiators: Clean Functional Polymers

ATRP is a successful method for precise polymer synthesis with controlled molecular weights and high chain end functionalities.

Micro Review of RAFT Polymerization

Micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization.

Yanfeng Xu et al.
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Chemotherapy is critical for the treatment of liver cancer. Despite the pro-apoptotic effects of corosolic acid (CA) have been revealed, the methods to enhance its efficacy are unclear. The aim of this study is to investigate the target that might
Ward Sents et al.
Cancer research, 77(24), 6825-6837 (2017-10-20)
Protein phosphatase 2A (PP2A) complexes counteract many oncogenic kinase pathways. In cancer cells, PP2A function can be compromised by several mechanisms, including sporadic mutations in its scaffolding A and regulatory B subunits or more frequently through overexpression of cellular PP2A
Christiane Trimpert et al.
PloS one, 12(9), e0183774-e0183774 (2017-09-21)
Regulation of our water homeostasis is fine-tuned by dynamic translocation of Aquaporin-2 (AQP2)-bearing vesicles to and from the plasma membrane of renal principal cells. Whereas binding of vasopressin to its type-2 receptor initiates a cAMP-protein kinase A cascade and AQP2
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Global Trade Item Number

SKUGTIN
723134-1G04061832861043
723134-250MG04061832861050