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Sigma-Aldrich

Poly(4-vinylpyridine-co-styrene)

powder

Synonym(s):

4-Vinylpyridine-styrene copolymer, Poly(4-vinylpyridine)-polystyrene copolymer, Styrene-4-vinylpyridine copolymer

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About This Item

CAS Number:
26222-40-2
MDL number:
MFCD00084388
UNSPSC Code:
12162002
NACRES:
NA.23

form

powder

Quality Level

100

application(s)

advanced drug delivery
coatings

SMILES string

C=CC1=CC=CC=C1.C=CC1=CC=NC=C1

InChI

1S/C8H8.C7H7N/c1-2-8-6-4-3-5-7-8;1-2-7-3-5-8-6-4-7/h2-7H,1H2;2-6H,1H2

InChI key

CIPXQVPZUWMSQE-UHFFFAOYSA-N

Related Categories

Application

Poly(4-vinylpyridine-co-styrene) can be used:
  • As a precursor in the preparation of ionic polymer with pendant photochromic moieties by reactingwith1,3,3-trimethyl-6′-bromohexyloxyspiro[2H]-indol-2,3′-[3H]-naphth[2,1-b][1,4]oxazine.
  • As permselective membrane in the preparation of composite electrodes for glucose sensing.
  • To prepare mixed redox polymer [RuIII(edta)(OH2)(py)]2[RuII(NH3)5(py)], which can switch into six redox states.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 8(9), 4885-4888 (2008-12-04)
An ionic polymer with pendant photochromic moieties was prepared by the reaction of poly(4-vinylpyridine-co-styrene) and 1,3,3-trimethyl-6'-bromohexyloxyspiro[2H]-indol-2,3'-[3H]-naphth[2,1-b][1,4]oxazine. The photochromic reaction in question is caused by the reversible heterolytic cleavage of the C(spiro)-O bond under UV irradiation, yielding the colored form that

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