Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic. For video creation, please contact our Academic Video Service.
Version Summary Created by Modification Content Size Created at Operation
1 handwiki Dean Liu -- 1049 2022-11-16 01:38:07

Video Upload Options

We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
HandWiki. Phthalocyanine Blue BN. Encyclopedia. Available online: https://encyclopedia.pub/entry/37634 (accessed on 23 September 2026).
HandWiki. Phthalocyanine Blue BN. Encyclopedia. Available at: https://encyclopedia.pub/entry/37634. Accessed September 23, 2026.
HandWiki. "Phthalocyanine Blue BN" Encyclopedia, https://encyclopedia.pub/entry/37634 (accessed September 23, 2026).
HandWiki. (2022, December 01). Phthalocyanine Blue BN. In Encyclopedia. https://encyclopedia.pub/entry/37634
HandWiki. "Phthalocyanine Blue BN." Encyclopedia. Web. 01 December, 2022.
Phthalocyanine Blue BN
Edit

Phthalocyanine Blue BN, also called by many names (EINECS 205-685-1), is a bright, crystalline, synthetic blue pigment from the group of phthalocyanine dyes. Its brilliant blue is frequently used in paints and dyes. It is highly valued for its superior properties such as light fastness, tinting strength, covering power and resistance to the effects of alkalis and acids. It has the appearance of a blue powder, insoluble in most solvents including water.

insoluble phthalocyanine alkalis

References

  1. Löbbert, Gerd (2000). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a20_213. . https://dx.doi.org/10.1002%2F14356007.a20_213
  2. Copper phthalocyanine chemblink.com http://www.chemblink.com/products/147-14-8.htm
  3. Toxic Substances Control Act Chemical Substance Inventory: volume 2
  4. Spectroscopic Properties of Inorganic and Organometallic Compounds: volume 40
  5. Chem Product Index by Friedrich W. Derz
  6. Coloring of Plastics: Fundamentals, r. Robert A. Charvat
  7. Paint and Coating Testing Manual, e. Joseph V. Koleske
  8. User guide and indices to the initial inventory, substance name index, US EPA
  9. Industrial Organic Pigments: Production, Crystal Structures, Properties, Applications by Klaus Hunger & Martin U. Schmidt
  10. The Porphyrin Handbook: Applications of Phthalocyanines, e. Karl Kadish, Kevin M. Smith & Roger Guilard
  11. Tattoo Inks: Analysis, Pigments, Legislation by Gerald Prior
  12. Pigment + Füllstoff: Tabellen by Olaf Lückert
  13. Material Safety Data Sheets Service 7:89, Information Handling Services
  14. Coloring of Food, Drugs, and Cosmetics by Gisbert Otterstätter
  15. Chemical Formulation: An Overview of Surfactant Based Chemical Preparations Used in Everyday Life by Anthony E. Hargreaves
  16. Waterloo Station: A History of London's busiest terminus by Robert Lordan
  17. COPPER PHTHALOCYANINE, CAS No.: 147-14-8 inchem.org http://www.inchem.org/documents/sids/sids/147148.pdf
  18. e.g. Structural and Transport Properties of Copper Phthalocyanine (CuPc) Thin Films www.egmrs.org http://www.egmrs.org/EJS/PDF/vo252/307.pdf
  19. Gregory, Peter (2000). "Industrial applications of phthalocyanines". Journal of Porphyrins and Phthalocyanines (worldscinet.com) 4 (4): 432–437. doi:10.1002/(SICI)1099-1409(200006/07)4:4<432::AID-JPP254>3.0.CO;2-N. http://www.worldscinet.com/jpp/04/0404/S1088424600000669.html. 
  20. https://incidecoder.com/ingredients/ci-74160
  21. https://kosterkeunen.com/formulas/color-deposition-conditioner-ultra-violet#post-5632
  22. Forensic Analysis of Tattoos and Tattoo Inks by Michelle D. Miranda, page 163: Muddy Water Blue
  23. https://hautschutzengel.de/_/produkt/51660.html#h2tab1a
  24. Szybowicz, M (October 2004). "High temperature study of FT-IR and Raman scattering spectra of vacuum deposited CuPc thin films". Journal of Molecular Structure 704 (1–3): 107–113. doi:10.1016/j.molstruc.2004.01.053. Bibcode: 2004JMoSt.704..107S.  https://dx.doi.org/10.1016%2Fj.molstruc.2004.01.053
  25. Wojdyla, Michal; Derkowska, Beata; Bala, Waclaw Bala (2005). "Lock-in phase analysis of copper phthalocyanine photoabsorption spectrum". Optica Applicata 35 (3): 561–571. 
  26. Bala, M; Wojdyla, M; Rebarz, M; Szybowic, M; Drozdowski, M; Grodzicki, A; Piszczek, P (2009). "Influence of central metal atom in MPc (M = Cu, Zn, Mg, Co) on Raman, FT-IR, absorbance, reflectance, and photoluminescence spectra". J. Optoelectron. Adv. M. 11 (3): 264–269. 
  27. Askat E, Jailaubekov (2013). "Hot charge-transfer excitons set the time limit for charge separation at donor/acceptor interfaces in organic photovoltaics". Nature Materials 12 (1): 66–73. doi:10.1038/nmat3500. PMID 23223125. Bibcode: 2013NatMa..12...66J.  https://dx.doi.org/10.1038%2Fnmat3500
  28. Xin, Li (January 2013). "CuPc/C60 bulk heterojunction photovoltaic cells with evidence of phase segregation". Organic Electronics 14: 250–254. doi:10.1016/j.orgel.2012.10.041.  https://dx.doi.org/10.1016%2Fj.orgel.2012.10.041
  29. Chaidogiannos, G.; Petraki, F.; Glezos, N.; Kennou, S.; Nešpůrek, S. (2009). "Low voltage operating OFETs based on solution-processed metal phthalocyanines". Applied Physics A 96 (3): 763. doi:10.1007/s00339-009-5268-1. Bibcode: 2009ApPhA..96..763C.  https://dx.doi.org/10.1007%2Fs00339-009-5268-1
  30. New material for quantum computing discovered out of the blue. phys.org. October 27, 2013 http://phys.org/news/2013-10-material-quantum-blue.html
  31. Warner, Marc (October 26, 2013). "New Material for Quantum Computing Discovered Out of the Blue". Nature. https://www.sciencedaily.com/releases/2013/10/131027185206.htm. 
  32. Quenqua, Douglas (November 4, 2013). "A Key to Quantum Computing, Close to Home". The New York Times. https://www.nytimes.com/2013/11/05/science/a-key-to-quantum-computing-close-to-home.html. 
  33. Gerd Löbbert "Phthalocyanines" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a20_213. https://doi.org/10.1002%2F14356007.a20_213
  34. P.Erk, H.Hengelsberg, M.F.Haddow, R.van Gelder (2004). "The innovative momentum of crystal engineering". CrystEngComm 6 (78): 474. doi:10.1039/b409282a.  https://dx.doi.org/10.1039%2Fb409282a
  35. H. S. Rzepa, www.ch.imperial.ac.uk/rzepa/blog/?p=3641, Accessed: 2011-03-08. (Archived by WebCite® at https://www.webcitation.org/5x2Q0jeBj) http://www.ch.imperial.ac.uk/rzepa/blog/?p=3641
  36. James H., Sharp; Martin, Abkowitz (1973). "Dimeric Structure of a Copper Phthalocyanine Polymorph". J. Phys. Chem. 77 (11): 477–481. doi:10.1021/j100623a012.  https://dx.doi.org/10.1021%2Fj100623a012
  37. Jacques M., Assour (1965). "On the Polymorphic Modifications of Phthalocyanines". J. Phys. Chem. 69 (7): 2295–2299. doi:10.1021/j100891a026.  https://dx.doi.org/10.1021%2Fj100891a026
  38. A.K., Hassan; R.D., Gould (2006). "Structural Studies of Thermally Evaporated Thin Films of Copper Phthalocyanine". Physica Status Solidi A 132 (1): 91–101. doi:10.1002/pssa.2211320110. Bibcode: 1992PSSAR.132...91H.  https://dx.doi.org/10.1002%2Fpssa.2211320110
  39. Hai, Wang; Soumaya, Mauthoor; Salahud, Din; Jules A., Gardener; Rio, Chang; Marc, Warner; Gabriel, Aeppli; David W., McComb et al. (June 7, 2010). "Ultralong Copper Phthalocyanine Nanowires with New Crystal Structure and Broad Optical Absorption". ACS Nano 4 (7): 3921–3926. doi:10.1021/nn100782w. PMID 20527798.  https://dx.doi.org/10.1021%2Fnn100782w
  40. Amy C, Cruickshank; Christian J, Dotzler; Salahud, Din; Sandrine, Heutz; Michael F, Toney; Mary P, Ryan (2012). "The crystalline structure of copper phthalocyanine films on ZnO(1100)". Journal of the American Chemical Society 134 (35): 14302–14305. doi:10.1021/ja305760b. PMID 22897507.  https://dx.doi.org/10.1021%2Fja305760b
  41. Safety data sheet cornelius.co.uk http://www.cornelius.co.uk/Documents/MSDS/Sitrament_Blue_GCN_(Blue_15.3)/$File/01030R-2%20gcn.pdf
  42. Sandor, S; Prelipceanu, O; Checiu, I (1985). "Sulphonated phthalocyanine induced caudal malformative syndrome in the chick embryo.". Morphol Embryol (Bucur) 31 (3): 173–81. PMID 2931590.  http://www.ncbi.nlm.nih.gov/pubmed/2931590
More
Upload a video for this entry
Information
Subjects: Others
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
View Times: 2.7K
Entry Collection: HandWiki
Revision: 1 time (View History)
Update Date: 01 Dec 2022
Notice
You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
OK
Confirm
Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?
Yes
No
${ textCharacter }/${ maxCharacter }
Submit
Cancel
There is no comment~
${ textCharacter }/${ maxCharacter }
Submit
Cancel
${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
Submit
Cancel
Confirm
Are you sure to Delete?
Yes No
Academic Video Service