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2,2'-Biimidazole

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CAS:492-98-8
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2,2'-Biimidazole manufacturers

  • 2,2'-Biimidazole
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  • $1.00
  • 2026-08-07
  • CAS:492-98-8
  • Min. Order: 1KG
  • Purity: 95%
  • Supply Ability: 200000KG
  • 2,2'-BIIMIDAZOLE
  • 2,2'-BIIMIDAZOLE pictures
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  • 2026-03-20
  • CAS:492-98-8
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100 mt
  • 2,2'-BIIMIDAZOLE
  • 2,2'-BIIMIDAZOLE pictures
  • $1.00
  • 2019-07-06
  • CAS:492-98-8
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 200KG
2,2'-Biimidazole Basic information
Product Name:2,2'-Biimidazole
Synonyms:bisimidazole;LABOTEST-BB LTBB005450;2-(1H-imidazol-2-yl)-1H-imidazole;1H,1'H-[2,2']BIIMIDAZOLYL;2,2'-Biimidazolyl;2,2'-Bisimidazole;2,2'-Diimidazole;Glycosine of Debus
CAS:492-98-8
MF:C6H6N4
MW:134.14
EINECS:207-768-8
Product Categories:
Mol File:492-98-8.mol
2,2'-Biimidazole Structure
2,2'-Biimidazole Chemical Properties
Melting point >350°C
Boiling point 455.5±28.0 °C(Predicted)
density 1.371±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pkapK1: 5.01(+1) (25°C,μ= 0.3)
color Light yellow to Brown to Dark green
λmax274nm(HCl aq.)(lit.)
InChIInChI=1S/C6H6N4/c1-2-8-5(7-1)6-9-3-4-10-6/h1-4H,(H,7,8)(H,9,10)
InChIKeyAZUHIVLOSAPWDM-UHFFFAOYSA-N
SMILESC1(C2NC=CN=2)NC=CN=1
Safety Information
Hazard Codes Xi
HS Code 2933.29.4300
HazardClass IRRITANT
MSDS Information
2,2'-Biimidazole Usage And Synthesis
Chemical Properties2,2'-Biimidazole is soluble in polar solvents such as methanol, water and dimethyl sulfoxide (DMSO).
Uses1H,1''H-2,2''-Biimidazole is used in the preparation of complexes that exhibits photoluminescence and optical properties. Also used in the preparation of bismuth biimidazoles as semi-conductors.
Application2,2'-Biimidazole is an important organic reagent used as:
(1) Preparation of catalytically active coordination compounds. It is a Lewis base capable of producing coordination compounds with metal ions such as Cu(I), Ag(I), Au(I-II) and palladium, which are used as efficient catalysts in other chemical reactions.
(2) Construction of hypercrosslinked polymers 2,2′-biimidazolyl HCPs, which are used as adsorbents and sensors for iodine capture and DNP detection in the field of environmental remediation.
(3) Synthesis of fluorescent proteins, nanoparticles and other ligand compounds.
Synthesis120 ml of distilled water was added to 1,092 g (14.2 mol, 4.0 eq.) of ammonium acetate at 40 ℃, 500 g of 20 wt percent aqueous glyoxal (3.45 mol) was then slowly added dropwise to the resulting slurry for three hours while stirring vigorously. Immediately after the addition was finished, the reaction mixture was neutralized with distilled water to adjust the pH to 5-7. The produced brown-colored solid was filtered and washed alternately with 500 ml of acetone and 500 ml of distilled water several times to obtain 82.0 g (53.2 percent yield) of 2,2'-Biimidazole.
References[1] Patent: US2003/199700, 2003, A1. Location in patent: Page/Page column 2
[2] Archiv der Pharmazie, 1986, vol. 319, # 2, p. 183 - 185
2,2'-Biimidazole Preparation Products And Raw materials
Raw materials1,2-Ethenediylbis(oxy) (9CI)-->Ammonium acetate
Preparation Products1,1-bis(pyridin-3-ylmethyl)-2,2-bisimidazole-->1,1-bis(pyridin-2-ylmethyl)-2,2-bisimidazole
Tag:2,2'-Biimidazole(492-98-8) Related Product Information
2,2'-BIS(4,5-DIMETHYLIMIDAZOLE) 2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole 2,2',4-Tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4',5'-diphenyl-1,1'-biimidazole 2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,1'-biimidazole 2,2'-BIBENZIMIDAZOLE 2,2'-Biimidazole 1-METHYL-1H,1'H-[2,2']BIIMIDAZOLYL 2-(1-METHYLIMIDAZOL-2-YL)-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID 1,1'-DIMETHYL-1H,1'H-[2,2']BIIMIDAZOLYL 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL 2,2'-BI-(IMIDAZOL-1-YL-ACETIC ACID) BI-(1,4,5-TRIMETHYL-IMIDAZOLE) 4,5-DIBROMO-2-(4,5-DIBROMOIMIDAZOL-2-YL)IMIDAZOLE 6,6'-DICHLORO-4,4'-DIMETHYL-1H,1'H-[2,2']BIBENZOIMIDAZOLYL 6-(1'-METHYL-[2,2']BIIMIDAZOLYL-1-YL)HEXYLAMINE HCL 4,4'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL (1'-METHYL-1'H-[2,2']BIIMIDAZOLYL-1-YL)ACETIC ACID 2,2'-BI-[N-(2-AMINO-ETHYL)IMIDAZOLE] 4HCL