What is the POLY(4-VINYLPHENOL)?

POLY(4-VINYLPHENOL) is , while it's Molecular Formula is C8H8O. Poly(p-hydroxystyrene) can substitute for Novolac resins in photoresists, adhesion promoter and improves heat resistance in hot melt adhesives and surface treatment in metal finishing. Derivatives used as antioxidants and flame retardants in plastics. Component of polymer blends to modify surface characteristics and improve impact resistance.

What is the CAS number for POLY(4-VINYLPHENOL)?

The CAS number of POLY(4-VINYLPHENOL) is 24979-70-2.

Reliable factory customized supply PVP 24979-70-2

Molecular Formula:C8H8O
Molecular Weight:120.150001525879
Vapor Pressure:0.168mmHg at 25°C
Melting Point:360oC (dec.)
Refractive Index:n20/D 1.6
Boiling Point:206.2°C at 760 mmHg
Flash Point:308°C
PSA：20.23000
Density:1.16 g/mL at 25 °C(lit.)
LogP:2.03520

POLY(4-VINYLPHENOL)(Cas 24979-70-2) Usage

General Description

Poly(4-vinylphenol) (PVP) is a polymeric cross-linker mainly used as a layer to improve adhesion by forming a non-toxic and low cost film. It is an acidic polymer which consists of more than 100 hydroxyl groups in one molecule of PVP which result in high stability and complexation of the films.

InChI:InChI=1/C8H8O/c1-2-7-3-5-8(9)6-4-7/h2-6,9H,1H2

24979-70-2 Relevant articles

Obtaining 4-vinylphenols by decarboxylation of natural 4-hydroxycinnamic acids under microwave irradiation

Bernini, Roberta,Mincione, Enrico,Barontini, Maurizio,Provenzano, Gianfranco,Setti, Leonardo

, p. 9663 - 9667 (2007)

4-Vinylphenols, useful compounds for ind...

-

Schmid,Karrer

, p. 722,738 (1945)

Phosphorus- And Sulfur-Containing High-Refractive-Index Polymers with High Tg and Transparency Derived from a Bio-Based Aldehyde

Fang, Linxuan,Sun, Jing,Chen, Xiaoyao,Tao, Yangqing,Zhou, Junfeng,Wang, Caiyun,Fang, Qiang

, p. 125 - 131 (2020)

Two flexible and colorless polymers are ...

Monitoring hydroxycinnamic acid decarboxylation by lactic acid bacteria using high-throughput UV-Vis spectroscopy

García-Cano, Israel,Giusti, M. Monica,Jiménez-Flores, Rafael,Miyagusuku-Cruzado, Gonzalo,Rocha-Mendoza, Diana

, (2020)

Hydroxycinnamic acid (HCA) decarboxylati...

4-Vinylphenyl Glycidyl Ether: Synthesis, RAFT Polymerization, and Postpolymerization Modifications with Alcohols

McLeod, David C.,Tsarevsky, Nicolay V.

, p. 1135 - 1142 (2016)

4-Vinylphenyl glycidyl ether (4VPGE), an...

Facile synthesis and characterization of highly branched polystyrene by self-condensing atom transfer radical polymerization

Lee, Jun Hyup

, p. 46 - 51 (2017)

To simply prepare hyperbranched polystyr...

Novel Amination and 1,2-Amino,hydro-Elimination between 2,3-Diketopyrido[4,3,2-de]quinolines and Primary Amino Compounds

Ding, Qizhu,Lown

, p. 7965 - 7972 (1999)

A novel animation and 1,2-amino,hydro-el...

Microbial transformations of p-Coumaric acid by Bacillus megaterium and Curvularia lunata

Torres y Torres,Rosazza

, p. 1408 - 1414 (2001)

p-Coumaric acid (1) is an abundant pheno...

Two-photon induced isomerization through a cyaninic molecular antenna in azo compounds

Villatoro, Emmanuel,Mu?oz-Rugeles, Leonardo,Durán-Hernández, Jesús,Salcido-Santacruz, Bernardo,Esturau-Escofet, Nuria,López-Cortés, Jose G.,Ortega-Alfaro, M. Carmen,Peón, Jorge

, p. 3123 - 3126 (2021)

We present a new design for non-linear o...

-

Sovish

, p. 1345,1346 (1959)

Characterization of the p-coumaric acid decarboxylase from Lactobacillus plantarum CECT 748T

Rodriguez, Hector,Landete, Jose Maria,Curiel, Jose Antonio,De Las Rivas, Blanca,Mancheno, Jose Miguel,Munoz, Rosario

, p. 3068 - 3072 (2008)

It was previously reported that cell cul...

Tetrazolation of side chains and anhydrous conductivity in a hydrophobic polymer

Ricks-Laskoski, Holly L.,Chaloux, Brian L.,Deese, Stephen M.,Laskoski, Matthew,Miller, Joel B.,Buckley, Mary A.,Baldwin, Jeffrey W.,Hickner, Michael A.,Saunders, Kaitlin M.,Christensen, Caroline M.

, p. 4243 - 4250 (2014)

1H-Tetrazoles possess the lowest pKa wit...

Antioxidant properties of 4-vinyl derivatives of hydroxycinnamic acids

Terpinc, Petra,Polak, Toma?,?egatin, Nata?a,Hanzlowsky, Andrej,Ulrih, Nata?a Poklar,Abramovi?, Helena

, p. 62 - 69 (2011)

The compounds 4-vinylphenol (4-VP), 4-vi...

Preparation of 4-vinylphenol using pHCA decarboxylase in a two-solvent medium

Ben-Bassat, Arie,Breinig, Sabine,Crum, Grace A.,Huang, Lixuan,La Bonte Altenbaugh, Amee,Rizzo, Nancy,Trotman, Robert J.,Vannelli, Todd,Sariaslani, F. Sima,Haynie, Sharon L.

, p. 278 - 285 (2007)

An efficient synthesis of 4-vinylphenol ...

3D-Printed Phenacrylate Decarboxylase Flow Reactors for the Chemoenzymatic Synthesis of 4-Hydroxystilbene

Peng, Martin,Mittmann, Esther,Wenger, Lukas,Hubbuch, Jürgen,Engqvist, Martin K. M.,Niemeyer, Christof M.,Rabe, Kersten S.

, p. 15998 - 16001 (2019)

Continuous flow systems for chemical syn...

Novel anionic photoacid generators (PAGs) and corresponding PAG bound polymers for sub-50 nm EUV lithography

Wang, Mingxing,Gonsalves, Kenneth E.,Rabinovich, Monica,Yueh, Wang,Roberts, Jeanette M.

, p. 1699 - 1706 (2007)

A new series of anionic photoacid genera...

Aromatic vs. aliphatic hyperbranched polyphosphoesters as flame retardants in epoxy resins

Markwart, Jens C.,Battig, Alexander,Velencoso, Maria M.,Pollok, Dennis,Schartel, Bernhard,Wurm, Frederik R.

, (2019)

The current trend for future flame retar...

Synthesis method of hydroxyl-substituted styrene compound and synthesis method of photoresist resin monomer

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Paragraph 0006; 0083-0085, (2022/01/12)

The present invention provides a synthes...

MODIFIED MONOMER, MODIFIED POLYMER COMPRISING THE SAME AND METHOD FOR PREPARING THEM

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Paragraph 0188-0191, (2021/05/18)

A modified monomer useful for the polyme...

Copper(ii)-catalyzed protoboration of allenes in aqueous media and open air

Nekvinda, Jan,Santos, Webster L.,Snead, Russell F.

supporting information, p. 14925 - 14931 (2021/09/04)

A method has been developed for the faci...

Rapid biosynthesis of phenolic glycosides and their derivatives from biomass-derived hydroxycinnamates

Zhao, Mingtao,Hong, Xulin,Abdullah,Yao, Ruilian,Xiao, Yi

, p. 838 - 847 (2021/02/09)

Biomass-derived hydroxycinnamates (mainl...

24979-70-2 Process route

: 19704-86-0
N,N-dimethyl-L-tyrosine N-oxide

: 5725-96-2
N,N-dimethylhydroxylamine

: 7400-08-0,50940-26-6
p-Coumaric Acid

: 2628-17-3,24979-70-2
4-Vinylphenol

Conditions

Conditions	Yield
In N,N-dimethyl acetamide; at 130 ℃; Product distribution / selectivity;	75% 3.3%

: 50-99-7
D-glucose

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 2628-17-3,24979-70-2
4-Vinylphenol

: 621-82-9
Cinnamic acid

Conditions

Conditions	Yield
With E_. coli strain WWQ_51.1; at 35 ℃; for 50h; pH=6.8 - 7.0; Microbiological reaction;

24979-70-2 Upstream products

123-07-9
4-Ethylphenol
2628-16-2
p-acetoxystyrene
7400-08-0
p-Coumaric Acid
32568-59-5
4-vinylphenyl benzoate

24979-70-2 Downstream products

32568-59-5
4-vinylphenyl benzoate
156366-10-8
1-(2-{2-[2-Hydroxy-3-(4-vinyl-phenoxy)-propoxy]-ethoxy}-ethoxy)-3-(4-vinyl-phenoxy)-propan-2-ol
156366-11-9
1-[2-(2-{2-[2-Hydroxy-3-(4-vinyl-phenoxy)-propoxy]-ethoxy}-ethoxy)-ethoxy]-3-(4-vinyl-phenoxy)-propan-2-ol
156366-12-0
1-{2-[2-(2-{2-[2-Hydroxy-3-(4-vinyl-phenoxy)-propoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-3-(4-vinyl-phenoxy)-propan-2-ol

PVP