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| Names | |
|---|---|
| IUPAC name disodium;2-[[4-[ethyl-[(3-sulfonatophenyl)methyl]amino]phenyl]-[4-[ethyl-[(3-sulfonatophenyl)methyl]azaniumylidene]cyclohexa-2,5-dien-1-ylidene]methyl]benzenesulfonate | |
Other names
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| Identifiers | |
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3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider |
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| ECHA InfoCard | 100.021.219 |
| EC Number |
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| E number | E133(colours) |
| KEGG | |
| UNII | |
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| Properties | |
| C37H34N2Na2O9S3 | |
| Molar mass | 792.85 g/mol |
| Melting point | 283 °C (decomposes) |
| soluble | |
| Hazards | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Brilliant blue FCF (Blue 1) is a syntheticorganic compound used primarily as a bluecolorant for processed foods, medications, dietary supplements, and cosmetics.[1] It is classified as atriarylmethane dye and is known under various names, such as FD&C Blue No. 1 or acid blue 9. It is denoted byE numberE133 and has acolor index of 42090. It has the appearance of a blue powder and is soluble in water and glycerol,[2] with a maximum absorption at about 628nanometers.[3] It is one of the oldest FDA-approved color additives, having been permanently listed for use in food and ingested drugs in 1969. It is generally considered nontoxic and safe for consumption.[4][5][6]
Brilliant blue FCF is asyntheticdye produced by thecondensation of 2-formylbenzenesulfonic acid and the appropriate aniline followed by oxidation.[7] It can be combined withtartrazine (E102) to produce various shades of green.
It is usually a disodium salt. The diammonium salt has CAS number 2650-18-2.[8] Calcium and potassium salts are also permitted. It can also appear as an aluminiumlake. The chemical formula is C37H34N2Na2O9S3.
Related dyes are C.I. acid green 3 (CAS#4680-78-8[9]) and acid green 9 (CAS#4857-81-2[10]). In these dyes, the 2-sulfonic acid group is replaced by H and Cl, respectively.[11]
Many attempts have been made to find similarly colored natural dyes that are as stable as brilliant blue FCF. Blue pigments must possess many chemical traits, including pi-bond conjugation, aromatic rings,heteroatoms and heteroatom groups, and ionic charges in order to absorb low energy red light. Most natural blue dyes are either unstable, blue only in alkaline conditions, or toxic; good candidates for further research into use as natural dyes includeanthocyanin andtrichotomine derivatives. No replacement for brilliant blue FCF has been found for use in beverages.[12][disputed –discuss]
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Like many other color additives, the primary use of Blue No. 1 is to correct or enhance natural coloring or to give colorless compounds a vivid hue.[13]
In the United States, of the two approved blue dyes (the other beingIndigo carmine, or FD&C Blue #2), brilliant blue FCF is the more common of the two. As a blue color, brilliant blue FCF is often found incotton candy,ice cream,canned processedpeas, packet soups, bottledfood colorings, icings, ice pops,blueberry flavored products, children's medications,dairy products, sweets[14]soft drinks, and drinks, especially the liqueurBlue Curaçao. It is also used insoaps,shampoos,mouthwash[15] and other hygiene and cosmetics applications.
Brilliant blue FCF is extensively used as a water tracer agent.[16] Due to its ability to retain color for long periods of time, brilliant blue FCF outperforms other dye tracers. Additionally, brilliant blue FCF has a low toxicity level that is favorable for the environment. However, brilliant blue FCF has different impacts on varying soils. Brilliant blue FCF is attracted to andsorbed in acidic soils due to its large size and ionic charge. Soil composition andflow velocity also affect the level of sorption of brilliant blue FCF.[17]
Brilliant blue FCF dye within beverages items—such as soda—can be used in theblue bottle experiment. In such foods, both the dye andreducing agents are incorporated in the same solution. When the solution is blue, oxygen is present. On the addition of NaOH, a reaction occurs that removes the oxygen, turning the solution clear. The dye turns back to blue once it is reoxidized by swirling the solution, incorporating oxygen from the air as anoxidizing agent.[18]
When applied to the tongue or to shaven skin, brilliant blue FCF can be absorbed directly into the bloodstream.[19] However, it is poorly absorbed from the gastrointestinal tract, and 95% of the ingested dye can be found in the feces.[citation needed]
Due to its nontoxic properties, brilliant blue FCF has been used as a biological stain. When dissolved in an acidic medium, this dye has been used to stain cell walls, bacteria, and fungal cells. The dye does not inhibit the growth of any of these species.[20]
For similar reasons, brilliant blue FCF is also being utilized inhemostatic medical devices, most notably the Hemopatch—designed to be placed on bleeding tissues and coagulate the blood. A low concentration of brilliant blue FCF is placed on the backside of the Hemopatch at 1 cm increments, allowing surgeons to cut precisely and indicate the side of the Hemopatch that is an active hemostatic agent for correct placement.[21]
Brilliant blue FCF is an approved food colorant and pharmacologically inactive substance for drug formulations in the EU and the United States. It is also legal in other countries. In a 1979 clinical trial of patients with perennial asthma, brilliant blue FCF, tested alongside two other non-azobenzene dyes (Erythrosine &Indigotin), was found to have no effect on pulmonary function in 42 of 43 participants.[22] This indicates that brilliant blue FCF is highly unlikely to causeallergic reactions in individuals with pre-existing moderate asthma. But, a case study of a 55-year-old man in 1996 reporting occupational asthma when exposed toIndigotine (a derivative ofIndigotin) at work found reduced pulmonary function could be recapitulated under laboratory conditions upon exposure;[23] suggesting that there may be some people sensitive to non-azobenzene dyes or justIndigotin particularly. In 2003, the U.S. FDA issued a public health advisory to warn health care providers of the potential toxicity of this synthetic dye in enteral feeding solutions.[24]The following legal limits apply in the EU (E 133) and other countries: 150–300 mg/kg depending on the type of food. Safety limit for foods and drugs: 0.1 mg/day per kg body weight.[25]Theacceptable daily intake for brilliant blue FCF is 6 mg/kg.
Brilliant blue FCF and similar dyes such as brilliant blue G are inhibitors topurinergic receptors—receptors that are responsible for inflammatory responses and other cell process.[26]
Scientists who were conductingin-vivo studies of compounds to lessen the severity of inflammation following experimentalspinal cord injury had previously tested a compound called OxATP to block a keyATP receptor in spinalneurons. However, OxATP has toxic side effects and must be injected directly into the spinal cord; in searching for alternatives they noted that brilliant blue FCF has a similar structure. This led them to test a related dye, brilliant blue G (also known asCoomassie brilliant blue) in rats, which improved recovery from spinal cord injury while temporarily turning them blue.[27]
When human washed platelets are evaluated usingturbidimetry it was found that brilliant blue FCF affectsplatelet aggregation by blocking thePanx1 channels. These inhibitory effects on collagen-induced shape change and maximal aggregation were shown by high (1 mM) concentrations of the dye but not by lower concentrations (100 μM). The 1 mM effective concentration is 1.59 times greater than the approximately 0.63 mM maximal allowable brilliant blue FCF concentration according to the European Food Safety Authority.[28]
Scientists are performing studies to better understand the effects of brilliant blue FCF duringveingraft explantation. Brilliant blue FCF hinders thepurinergic receptors, limiting cell proliferation that may lead tointimal hyperplasia. The effects of brilliant blue FCF were tested on rat aortic cells. It was found that brilliant blue FCF had a positive impact in limiting the development of intimal hyperplasia following a vein graft procedure.[29][30]
porcine tongue dorsum was exposed to human saliva with 15,000 ng/cm2 of dye for 20 min. 24-h diffusion resulted in 34 ng/cm2 of BB and 86 ng/cm2 of PB which can be directly absorbed into the blood system.
