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Postion:Product Catalog >2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole
2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole
  • 2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole

2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole NEW

Price Get Latest Price
Package 1kg 25kg
Min. Order: 1kg
Supply Ability: 30MT/Month
Update Time: 2024-05-27

Product Details

Product Name: 2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole CAS No.: 7189-82-4
EC-No.: 230-555-6 Min. Order: 1kg
Purity: 99% Supply Ability: 30MT/Month
Release date: 2024/05/27

7189-82-4 - Names and Identifiers

Name2,2'-Bis(O-Chlorophenyl)-4,4',5,5'-Tetraphenyl-1,2'-Bi (III-Imidazole)
SynonymsKSBC
INBC
BCIM
Photopolymerizationinitiator
2,2'-di-(o-nitrophenoxy)-biphenyl
2,2-Bis(2-chlorophenyl)-4,4,5,5-tetraphenyl-1,2-biimidazole
2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazo
2,2'-Bis(2-chlorophenyl)-4,4'5,5'-tetraphenyl-1,2'-biimidazole
2,2'-Bis(o-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole
2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole
2,2'-Bis(2-chlorophenyl)-4,5,4',5'-tetraphenyl-1,2'-biimidazole
2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-2'H-1,2'-biimidazole
2,2'-bis(o-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-bi(iii-imidazole)
2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole (BCIM)
2,2'-Bis(O-Chlorophenyl)-4,4',5,5'-Tetraphenyl-1,2'-Bi (III-Imidazole)
2-(2-CHLOROPHENYL)-1-[2-(2-CHLOROPHENYL)-4,5-DIPHENYL-IMIDAZOL-2-YL]-4,5-DIPHENYL-IMIDAZOLE
CAS7189-82-4
EINECS230-555-6
InChIInChI=1/C42H28Cl2N4/c43-35-27-15-13-25-33(35)41-45-39(31-21-9-3-10-22-31)40(32-23-11-4-12-24-32)48(41)42(34-26-14-16-28-36(34)44)46-37(29-17-5-1-6-18-29)38(47-42)30-19-7-2-8-20-30/h1-28H

7189-82-4 - Physico-chemical Properties

Molecular FormulaC42H28Cl2N4
Molar Mass659.6
Density1.24±0.1 g/cm3(Predicted)
Melting Point194°C
Boling Point810.3±75.0 °C(Predicted)
Flash Point443.9°C
Vapor Presure0-0Pa at 20-25℃
AppearanceSolid:crystalline
ColorLight yellow to Yellow to Green
pKa3.37±0.10(Predicted)
Storage ConditionRoom Temprature
Refractive Index1.675
MDLMFCD00060081

7189-82-4 - Risk and Safety

HS Code29339900

7189-82-4 - Reference Information

LogP7.6 at 35℃ and pH9
EPA chemical substance informationinformation provided by: ofmpeb.epa.gov (external link)
Applicationhexaaryl biimidazoles are a class of organic compounds (abbreviated as ABI), typically hexaphenyl biimidazoles. 2,2 '-bis (2-chlorophenyl)-4,4'5,5'-tetraphenyl-1, 2 '-bis-imidazole is The photoinitiator O-chlorohexaaryl bis-imidazole (BCIM), the existing synthesis method is to use sodium hypochlorite as the oxidation condensation agent for the synthesis of BCIM, which brings more alkaline "wastewater" with low yield and high cost.
preparationA preparation method of diimidazole photoinitiator, the specific steps are as follows:(1) add 30% ml of water or the previous batch of reaction mother liquor and 50g of 1 ml liquid alkali into a 100 ml glass reaction flask, stir and mix well;(2) add g of BCIM-monomer wet material, stir for 15 minutes, then add 300g of dichloromethane and 6g of dodecyldimethyl benzyl ammonium chloride;(3) Keep the temperature at 20-35 ° C., slowly drop 50g of 30% hydrogen peroxide for 4-6 hours, add it and stir for 60 minutes;(4) sample for liquid chromatography analysis; If the weight percentage of unreacted BCIM-monomer wet material is more than 0.5%, add 30% hydrogen peroxide, the weight is 2 times the weight of the unreacted BCIM-monomer wet material analyzed by liquid chromatography;(5) stirring for 1 hour, repeating the 4th step, until the unreacted BCIM-monomer wet material content is less than 0.5% by weight; (6) the reaction solution is poured into a 1000ml separatory funnel, and allowed to stand for 15 minutes to clarify, and then the aqueous layer is separated;(7) 200ml of water is added to the dichloromethane layer, and after stirring for 5 minutes, (8) separate the washed water layer, add deionized water, stir for 30 minutes, and then stand for 1 hour;(9) Pour the organic layer into a 500ml distillation flask, dichloromethane can be recovered by heating under normal pressure, and the dichloromethane recovered by distillation can be used for the next batch of reaction;(10) add 200ml isopropanol, continue distillation, and stop distillation when the reaction solution becomes turbid;(11) under stirring, add cold water, cool to room temperature, and filter; (12) the filter cake was slightly washed twice with fresh isopropanol;(13) dried in a drying cabinet to give 93-95g of yellow BCIM crystals in 93%-95% yield.


Company Profile Introduction

Shijiazhuang Jianxin Biotechnology Co., Ltd. was established in December 2023 with a registered capital of five hundred thousand yuan, located in Xingtang Chemical Industry Park, Shijiazhuang City, Hebei Province. It is an important part of Xingtang Development Zone and a key chemical new material enterprise. Adhering to the concept of integrity, green, innovation and win-win development, with a strong R & D team and scientific management mode, the company is committed to the technology development, technology transformation and production and operation of new energy materials. The company has 48 employees, including 12 R&D personnel. Since 2023, it has successfully researched and developed electrolyte additives such as 1, 3, 6-hexane trinitrile (HTCN), and pharmaceutical intermediates such as 2-phenylacetamide and tryptamine.

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Shijiazhuang Jianxin Biotechnology Co., LTD

1YR ChinaChina
  • Since: 2023-11-27
  • Address: No.17, Xinglong West Street, North Longgang Village, Nanqiao Town, Xingtang County, Shijiazhuang Cit
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