Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and Congo red: Difference between pages

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| verifiedrevid = 470446279

| Name = Congo red

| ImageFile = Congo-red-2D-skeletal.png

| ImageSize = 300

| ImageAlt = Skeletal formula of congo red

| ImageFile1 = Congo-red-sodium-3D-spacefill.png

| ImageSize1 = 280

| ImageAlt1 = Space-filling model of the component ions of congo red

| IUPACName = disodium 4-amino-3-[4-[4-(1-amino-4-sulfonato-naphthalen-2-yl)diazenylphenyl]phenyl]diazenyl-naphthalene-1-sulfonate

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| Section1 = {{Chembox Identifiers

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| PubChem=11313

| SMILES = [Na+].[Na+].[O-]S(=O)(=O)c5cc(/N=N/c1ccc(cc1)c4ccc(/N=N/c3cc(c2ccccc2c3N)S([O-])(=O)=O)cc4)c(N)c6c5cccc6

| MeSHName=Congo+red

| Section2 = {{Chembox Properties

| Formula=C₃₂H₂₂N₆Na₂O₆S₂

| MolarMass=696.665

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| Section3 = {{Chembox Hazards

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[[File:Конго красный.jpg|alt=Congo red solid and in solution|thumb|Congo red solid and in water solution]]

'''Congo red''' is an [[organic compound]], the sodium salt of 3,3′-([1,1′-biphenyl]-4,4′-diyl)bis(4-aminonaphthalene-1-sulfonic acid). It is an [[azo dye]]. Congo red is water-soluble, yielding a red [[colloid]]al solution; its solubility is greater in organic solvents. The use of Congo red in the textile industry has long been abandoned, primarily because of its carcinogenic properties,<ref name=Azodye>Klaus Hunger, Peter Mischke, Wolfgang Rieper, Roderich Raue, Klaus Kunde, Aloys Engel: "Azo Dyes" in ''Ullmann's Encyclopedia of Industrial Chemistry'', 2005, Wiley-VCH, Weinheim.{{doi|10.1002/14356007.a03_245}}.</ref> but it is still used for [[Staining (biology)|histological staining]].

== History ==

Congo red was first synthesized in 1883 by Paul Böttiger, who had been employed at Friedrich [[Bayer]] Company in Elberfeld, Germany. He was looking for [[Substantive dye|textile dyes that did not require]] a [[mordant]] step. The company which had a [[right of first refusal]] to his inventions was not interested in this bright red color, so he filed the patent under his own name and sold it to the [[AGFA]] company of Berlin. AGFA marketed the dye under the name "Congo red", a catchy name in Germany at the time of the 1884 [[Berlin Conference|Berlin West Africa Conference]], an important event in the [[Colonisation of Africa]]. The dye was a major commercial success for AGFA. In the following years, for the same reason, other dyes were marketed using the "Congo" name: Congo rubine, Congo corinth, brilliant Congo, Congo orange, Congo brown, and Congo blue.<ref>{{ cite journal | author = Steensma, D. P. | year = 2001 | title = Congo Red: Out of Africa? | journal = Archives of Pathology and Laboratory Medicine | volume = 125 | issue = 2 | pages = 250–252 | doi = 10.5858/2001-125-0250-CR | pmid = 11175644 | url = http://www.archivesofpathology.org/doi/pdf/10.1043/0003-9985%282001%29125%3C0250%3ACR%3E2.0.CO%3B2 | format = pdf }}{{dead link|date=August 2017 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> Once of economic significance, Congo red has fallen into disuse as have all [[benzidine]]-derived dyes, owing to their carcinogenic activity.

It is prepared by azo coupling of the bis(diazonium) derivative of [[benzidine]] with [[naphthionic acid]].<ref name=Ullmann>Gerald Booth "Naphthalene Derivatives" in [[Ullmann's Encyclopedia of Industrial Chemistry]], 2005, Wiley-VCH, Weinheim. {{doi|10.1002/14356007.a17_009}}.</ref>

Congo blue, however, is in widespread international use, in gel sheet form, as a filter to place in front of theatrical, motion picture, television, church, and live event lighting instruments. It is sold under the item name "181 Congo Blue" by [[Lee Filters]]. It emits a deep rich saturated blue color with elements of red. Depending upon the color temperature of the source lamp, the light from a lighting instrument with a Congo Blue filter reflected from a white surface can vary from very saturated blue to purple or violet. The manufacturer reports that fluorescent light through a Congo Blue filter gives the appearance of black light.<ref>{{Cite web |title=LEE 181: Congo Blue Filter - Congo Blue Gel |url=https://leefilters.com/colour/181-congo-blue/ |access-date=2023-03-09 |website=LEE Filters |language=en-US}}</ref> Congo Blue filters are frequently used at live music concerts at an angle from behind musicians to cross back-light with a "warm" color gel like yellow, straw, gold, orange, or magenta, from an opposing angle, for a very dramatic effect. Another use of Congo Blue filters by lighting technicians, is to cut a small strip from the gel sheet, which the technician looks through to make brightness adjustments to a video monitor displaying a standard color bar chart. The Congo Blue filter effectively removes the color from chart and shows the separate bars only in terms of their differing incremental brightness levels. This allows the technician to adjust the monitor to show a full and correct range of brightnesses.

== Behavior in solution ==

{{pH_indicator_template|indicator_name=Congo red|low_pH=3.0|high_pH=5.2|low_pH_color=blue|low_pH_text=white|high_pH_color=red|high_pH_text=white}}

Due to a color change from blue to red at [[pH]]&nbsp;3.0–5.2, Congo red can be used as a [[pH indicator]]. Since this color change is an approximate inverse of that of [[litmus]], it can be used with litmus paper in a simple parlor trick: add a drop or two of Congo red to both an acid solution and a base solution. Dipping red litmus paper in the red solution will turn it blue, while dipping blue litmus paper in the blue solution will turn it red. This property gives Congo red a [[metachromatic]] property as a dye, both in strongly acidic solutions and with strongly [[acidophilic]] tissue.

Congo red has a propensity to aggregate in aqueous and organic solutions. The proposed mechanisms suggest hydrophobic interactions between the aromatic rings of the dye molecules, leading to a π–π [[Stacking (chemistry)|stacking]] phenomenon. Although these aggregates are present under various sizes and shapes, the "ribbon-like micelles" of a few molecules seem to be the predominant form (even if the "[[micelle]]" term is not an entirely appropriate name for it). This aggregation phenomenon is more prevalent in high Congo red concentrations, at high salinity and/or low pH.

== Diagnostic use ==

[[File:Cardiac amyloidosis very high mag.jpg|thumb|right|[[Micrograph]] demonstrating [[amyloid]] deposition (red-orange) with Congo red staining in [[cardiac amyloidosis]]]]

In [[histology]] and [[microscopy]], Congo red is used for [[Staining (biology)|staining]] in [[amyloidosis]], and for the [[cell walls]] of plants and fungi, and for the [[Bacterial outer membrane|outer membrane]] of [[Gram-negative bacteria]]. Apple-green [[birefringence]] of Congo red stained preparations under [[polarized light]] is indicative of the presence of amyloid fibrils. Additionally, Congo red is used for the diagnostics of the ''[[Shigella flexneri]]'' serotype 2a, where the dye binds the bacterium's unique [[lipopolysaccharide]] structure.

Furthermore, Congo red may also be used to induce expression of the type III secretion system of ''Shigella flexneri'', bringing about the secretion of IpaB and IpaC, which form translocation pores within host cell membrane, allowing effector proteins to pass through and alter the host cell's biochemistry. The dye can also be used in flow cytometry experiments for the detection of ''Acanthamoeba'', ''Naegleria'' and other amoebal cysts.

In confocal microscopy, Congo red can be used as a stable fluorescent stain.<ref>{{ cite journal | journal = Journal of Microscopy | author1 = Michels, J. | author2 = Büntzow, M. | year = 2010 | title = Assessment of Congo red as a fluorescence marker for the exoskeleton of small crustaceans and the cuticle of polychaetes | volume = 238 | issue = 2 | pages = 95–101 | doi = 10.1111/j.1365-2818.2009.03360.x | pmid = 20529057 | s2cid = 205342989 }}</ref>

==See also==

* [[Thioflavin]]

==References==

{{Reflist}}

{{Stains}}

[[Category:Azo dyes]]

[[Category:PH indicators]]

[[Category:Staining dyes]]

[[Category:Naphthalenesulfonates]]

[[Category:Naphthylamines]]

[[Category:Biphenyls]]

[[Category:Organic sodium salts]]

[[Category:Substances discovered in the 19th century]]