POLY(N-VINYLCARBAZOLE)

POLY(N-VINYLCARBAZOLE) Structure
CAS No.
25067-59-8
Chemical Name:
POLY(N-VINYLCARBAZOLE)
Synonyms
PVCz;PNVC;PNVK;PVCA;dh700;tuvical210;M.N. 56,400;luvicanm150;luvicanm170;M.N. 56,400 5GR
CBNumber:
CB3288478
Molecular Formula:
C42H33N3X2
Molecular Weight:
579.73
MOL File:
25067-59-8.mol
MSDS File:
SDS
Modify Date:
2024/7/2 17:04:22

POLY(N-VINYLCARBAZOLE) Properties

Melting point >300 °C
Density 1.2 g/mL at 25 °C(lit.)
Tg 227
refractive index n20/D 1.683
form powder
color Off-white
Stability Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 25067-59-8(CAS DataBase Reference)
EPA Substance Registry System 9H-Carbazole, 9-ethenyl-, homopolymer (25067-59-8)

SAFETY

Risk and Safety Statements

Safety Statements  24/25
WGK Germany  2
RTECS  FE6225480
TSCA  TSCA listed
HS Code  29339900
NFPA 704
0
1 0

POLY(N-VINYLCARBAZOLE) price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 182605 Poly(9-vinylcarbazole) average Mw ~1,100,000, powder 25067-59-8 5G ₹10770.88 2022-06-14 Buy
Sigma-Aldrich(India) 368350 Poly(9-vinylcarbazole) average Mn 25,000-50,000 25067-59-8 5G ₹15068.4 2022-06-14 Buy
Sigma-Aldrich(India) 182605 Poly(9-vinylcarbazole) average Mw ~1,100,000, powder 25067-59-8 25G ₹31111.05 2022-06-14 Buy
Product number Packaging Price Buy
182605 5G ₹10770.88 Buy
368350 5G ₹15068.4 Buy
182605 25G ₹31111.05 Buy

POLY(N-VINYLCARBAZOLE) Chemical Properties,Uses,Production

Chemical Properties

off-white crystalline powder

Uses

PVK:graphene oxide composite can be used as a hybrid film which can be coated on silica substrate for the fabrication of organic field effect transistors (OFETs). It can also form a nano-composite film with carbon nanospheres (CNS) which can be potentially used in supercapacitors and sensor based applications.

Definition

ChEBI: A macromolecule composed of repeating 9-ethylcarbazole units.

Preparation

N-Vinyl carbazole may be obtained from phenylhydrazine and cyclohexanone by the following route:

25067-59-8 synthesis


The second step in this synthesis is an example of the Fischer indole synthesis. Carbazole also occurs in coal tar.
Poly(vinyl carbazole) is produced by adiabatic bulk polymerization under nitrogen pressure using azobisisobutyronitrile and di-tert-butyl peroxide as initiators. Heating to 80-90??C causes an onset of polymerization and a rapid increase in temperature. After the maximum temperature has been reached the mass is cooled under pressure.
Poly(vinyl carbazole) is a very brittle material with a high softening point (about 195??C Vicat). It is insoluble in most organic solvents except aromatic and chlorinated hydrocarbons and tetrahydrofuran. The polymer is difficult to mould, requiring high process temperatures, namely about 300??C for injection moulding and 250??C for compression moulding. More usually the material is cast as thin film from solution. The most significant property of poly(vinyl carbazole) is its high photoconductivity and this has resulted in widespread use of the polymer in electrostatic dry-copying machines. When an electrostatic charge is applied to the polymer in the dark it discharges to an equilibrium value but when the polymer is illuminated almost complete discharging occurs. This phenomenon is used to create a latent electrostatic image which is then developed by transferring the charge to the toner.
Poly(vinyl carbazole) also has good electrical insulation characteristics which are maintained over a wide range of temperature and frequency. On account of these characteristics, the polymer has been used as a capacitor dielectric, but this application is now of minor importance.

General Description

Poly(9-vinylcarbazole) (PVK) is a conductive polymer which is mainly used as a hole transporting medium at high efficiencies with low driving voltage. It can also be used as an anode for hole injection and can act as an effective charge transferring gate by co-doping it with organic dyes.

Purification Methods

Precipitate it seven times from tetrahydrofuran with MeOH, with final freeze-drying from *benzene. Dry it under vacuum.

POLY(N-VINYLCARBAZOLE) Preparation Products And Raw materials

Global( 132)Suppliers
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TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
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Chemical Centre 91-22-22031616 Maharashtra, India 29 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20361 58 Inquiry
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Zhengzhou Alfa Chemical Co.,Ltd +8618530059196 China 12962 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418671 China 34571 58 Inquiry
Dayang Chem (Hangzhou) Co.,Ltd. 571-88938639 +8617705817739 China 52861 58 Inquiry
tuvical210 N-VINYLCARBAZOLE POLYMER POLYVINYL CARBAZOLE POLY(N-VINYLCARBAZOL) POLY(9-VINYLCARBAZOLE), SECONDARY STANDA RD Poly(N-vinylcarbazole), approx. M.W. 90,000 Poly(N-vinylcarbazole), secondary standard M.N. 56,400 Poly(N-vinylcarbazole), secondary standard, M.W. 135,600 9-Vinyl-9H-carbazole POLY(N-VINYLCARBAZOLE) POLY(9-VINYLCARBAZOLE) 9-ethenyl-9h-carbazolhomopolymer 9-vinylcarbazolehomopolymer 9-vinyl-carbazolpolymer dh700 luvicanm150 luvicanm170 Poly(9-vinylcarbazole) average Mn 25,000-50,000 Poly(9-vinylcarbazole) average Mw ~1,100,000, powder poly(vinylcarbazole) macromolecule n-vinylcarbazolehomopolymer polyvinyl carbazole (PVK) Poly(n-vinylcarbazole), secondary standard, MW. 135,600: MN. 56,400 9-Vinylcarbazole polymer Poly(9-vinyl-9H-carbazole) Poly(N-vinylcarbazole) [approx. M.W. 9000] Poly(9-vinylcarbazole),PVK PVK , Poly(N-vinylcarbazole) M.N. 56,400 5GR Poly(N-vinylcarbazole), approx. M.W. 90,000 10GR Poly(N-vinylcarbazole), approx. M.W. 90,000 25GR PVCz Poly(N-vinylcarbazole), average M.W. 90,000 PNVC PNVK Poly(9-ethenyl-9H-carbazole) Poly[1-(N-carbazolyl)ethylene] PVCA 25067-59-8 C42H33N3X2 -C12H6NHCHCH2n C12H8NCHCH2n POLB - POLY Alphabetic Electroluminescence Carbazoles (for Conduting Polymer Research) Carbazoles Reagents for Conducting Polymer Research Analytical Standards Analytical Chromatography Product Catalog Carbazoles Carbazoles (for Conduting Polymer Research) Electroluminescence Functional Materials Reagents for Conducting Polymer Research Electronic Chemicals