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Sigma-Aldrich

4,4′-Dinonyl-2,2′-dipyridyl

97%

Sinónimos:

dNbpy

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About This Item

Fórmula empírica (notación de Hill):
C28H44N2
Número de CAS:
142646-58-0
Peso molecular:
408.66
MDL number:
MFCD00800915
UNSPSC Code:
12352100
PubChem Substance ID:
24871818
NACRES:
NA.22

assay

97%

mp

61-63 °C (lit.)

SMILES string

CCCCCCCCCc1ccnc(c1)-c2cc(CCCCCCCCC)ccn2

InChI

1S/C28H44N2/c1-3-5-7-9-11-13-15-17-25-19-21-29-27(23-25)28-24-26(20-22-30-28)18-16-14-12-10-8-6-4-2/h19-24H,3-18H2,1-2H3

InChI key

VHJFWJXYEWHCGD-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

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Maryam Bozorg et al.
Soft matter, 16(4), 1066-1081 (2019-12-21)
Poly[oligo(ethylene oxide)] based gradient and random copolymers with different compositions are synthesized via Cu-based atom transfer radical polymerization. The solubility behavior of these copolymers in pure water and in the presence of different salts, surfactants and ethanol is investigated. According
Yi-Shen Huang et al.
Polymers, 11(6) (2019-06-27)
Atom transfer radical polyaddition (ATRPA) was utilized herein to synthesize a specific functional polyester. We conducted ATRPA of 4-vinylbenzyl 2-bromo-2-phenylacetate (VBBPA) inimer and successfully obtained a linear type poly(VBBPA) (PVBBPA) polyester with benzylic bromides along the backbone. To obtain a
Taeheon Lee et al.
Nanoscale, 7(15), 6745-6753 (2015-03-26)
We synthesized poly((furfuryl methacrylate)-co-(2-(dimethylamino)ethyl methacrylate)) (p(FMA-co-DMAEMA)) for the dispersion of single-walled carbon nanotubes (SWCNTs) while maintaining their high aspect ratios. The nanotubes' length and height were 2.0 μm and 2 nm, as determined by transmission electron microscopy and atomic force

Artículos

ATRP Ligands and Initiators for the Clean Synthesis of Functional Polymers

Atom transfer radical polymerization (ATRP) has emerged as one of the most successful synthetic techniques for the preparation of polymers with predetermined molecular weights, narrow molecular weight distributions, and high degrees of chain end functionalities.

ATRP: Complete Tools for the Synthesis of Well-Defined, Functionalized Polymers

Find how atom transfer radical polymerization (ATRP) tools can be used for the synthesis of well-defined functionalized polymers.

ATRP: Complete Tools for the Synthesis of Well-Defined Functionalized Polymers

ATRP polymerization, chain transfer agent, living polymerization, functional telechelic polymers

A Micro Review of Reversible Addition/Fragmentation Chain Transfer (RAFT) Polymerization

We presents an article about a micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization. RAFT (Reversible Addition/Fragmentation Chain Transfer) polymerization is a reversible deactivation radical polymerization (RDRP) and one of the more versatile methods for providing living characteristics to radical polymerization.

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Protocolos

Concepts and Tools for RAFT Polymerization

Sigma-Aldrich presents an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

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.

Typical Procedures for Polymerizing via ATRP

Sigma-Aldrich presents an article about the typical procedures for polymerizing via ATRP, which demonstrates that in the following two procedures describe two ATRP polymerization reactions as performed by Prof. Dave Hadddleton′s research group at the University of Warwick.

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