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Anthrimide

Base Information Edit
  • Chemical Name:Anthrimide
  • CAS No.:82-22-4
  • Molecular Formula:C28H15 N O4
  • Molecular Weight:429.431
  • Hs Code.:2922399090
  • European Community (EC) Number:201-405-7
  • NSC Number:7226
  • UNII:717ZXC72EA
  • DSSTox Substance ID:DTXSID4058865
  • Nikkaji Number:J4.609D
  • Wikidata:Q27265938
  • Mol file:82-22-4.mol
Anthrimide

Synonyms:Anthrimide;1,1'-Dianthrimide;82-22-4;1,1'-Iminodianthraquinone;1,1'-Dianthraquinonylamine;Dianthrimide;9,10-Anthracenedione, 1,1'-iminobis-;Dianthraquinonylamine;1,1-Dianthrimid;Imino-1,1'-bianthraquinone;Anthraquinonylaminoanthraquinone;Di-1,1'-anthrachinonylamin;Di(1-anthraquinoyl)amine;1,1-Dianthrimid [Czech];Bis-(1-anthrachinonyl)amin;NSC 7226;ANTHRAQUINONE, 1,1'-IMINODI-;1,1'-Azanediylbis(anthracene-9,10-dione);1-[(9,10-dioxoanthracen-1-yl)amino]anthracene-9,10-dione;Bis-(1-anthrachinonyl)amin [Czech];EINECS 201-405-7;Di-1,1'-anthrachinonylamin [Czech];Bis(1-anthraquinonyl)amine;BRN 2607016;UNII-717ZXC72EA;AI3-28933;717ZXC72EA;NSC7226;NSC-7226;4-14-00-00432 (Beilstein Handbook Reference);1,1'-Iminodianthraquinone [for Determination of Boron];C28H15NO4;1,1'-Dianthrimid;ANTHRIMIDE [MI];1,1'-iminodianthraquinon;9, 1,1'-iminobis-;AISE 4;Anthraquinone,1'-iminodi-;SCHEMBL42481;BIDD:GT0777;DTXSID4058865;1,1'-Iminodianthra-9,10-quinone;BIS(ANTHRAQUINON-1-YL)AMINO;1,1'-iminodianthracene-9,10-dione;C28-H15-N-O4;MFCD00019132;STK027253;AKOS015894668;1,1'-azanediyldianthracene-9,10-dione;LS-20696;CS-0357999;D0133;FT-0631373;1,1'-IMINOBIS-9,10-ANTHRACENEDIONE;T71363;W-109294;WLN: L C666 BV IVJ DM- DL C666 BV IVJ;Q27265938;1-[(9,10-dioxo-1-anthryl)amino]anthracene-9,10-dione

Suppliers and Price of Anthrimide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TCI Chemical
  • 1,1'-Iminodianthraquinone [for Determination of Boron] >98.0%(N)
  • 5g
  • $ 390.00
  • Crysdot
  • 1,1'-Azanediylbis(anthracene-9,10-dione) 97%
  • 100g
  • $ 612.00
  • American Custom Chemicals Corporation
  • 1,1'-DIANTHRIMIDE 95.00%
  • 10G
  • $ 1190.37
  • AK Scientific
  • 1,1'-Iminodianthraquinone
  • 5g
  • $ 549.00
  • AHH
  • 1,1'-Dianthraquinonylamine 98%
  • 250g
  • $ 406.00
Total 15 raw suppliers
Chemical Property of Anthrimide Edit
Chemical Property:
  • Appearance/Colour:Dark red powder 
  • Melting Point:300 °C  
  • Refractive Index:1.6290 (estimate) 
  • Boiling Point:544.01°C (rough estimate) 
  • PKA:-4.72±0.20(Predicted) 
  • Flash Point:221.6oC 
  • PSA:80.31000 
  • Density:1.2950 (rough estimate) 
  • LogP:5.05400 
  • XLogP3:5.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:429.10010796
  • Heavy Atom Count:33
  • Complexity:783
Purity/Quality:

98% *data from raw suppliers

1,1'-Iminodianthraquinone [for Determination of Boron] >98.0%(N) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 37/39-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Dyes -> Anthraquinone Dyes
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)NC4=CC=CC5=C4C(=O)C6=CC=CC=C6C5=O
  • Uses Determination of boron. 1,1'-Dianthrimide is used as a 0.02% solution in Concentrated H2SO4. The olive-green solution turns blue in the presence of boron. The blue solution has an absorption max at 620 nm. Also used in the determination of silicon.
Technology Process of Anthrimide

There total 7 articles about Anthrimide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium carbonate; nitrobenzene;
Guidance literature:
With copper diacetate; sodium carbonate; at 260 ℃;
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