Chemistry:Pararosaniline
From HandWiki
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| IUPAC name
[4-[Bis(4-aminophenyl)methylidene]-1-cyclohexa-2,5-dienylidene]dianiline
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| Other names
Pararosaniline
p-rosaniline C.I. 42500 Para magenta | |
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3D model (JSmol)
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PubChem CID
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| Properties | |
| C19H17N3 | |
| Molar mass | 323.83 g/mol |
| Appearance | Green crystalline solid |
| Melting point | 268 to 270 °C (514 to 518 °F; 541 to 543 K) decomposes |
| Slightly soluble | |
| Hazards | |
| Safety data sheet | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Pararosaniline, Basic Red 9, or C.I. 42500 is an organic compound with the formula [(H2NC6H4)3C]Cl. It is a magenta solid with a variety of uses as a dye.[1] It is one of the four components of basic fuchsine. (The others are rosaniline, new fuchsine and magenta II.)[2] It is structurally related to other triarylmethane dyes called methyl violets including crystal violet, which feature methyl groups on nitrogen.
It is prepared by the condensation of aniline and para-aminobenzaldehyde. Alternatively, it arises from the oxidation of 4,4'-bis(aminophenyl)methane in the presence of aniline.
Uses
- It is used to dye polyacrylonitrile fibers.
- It is used to detect sulfur dioxide.[3]
- Pararosaniline is used as a colorimetric test for aldehydes, in the Schiff test. It is the only basic fuchsine component suitable for making the aldehyde-fuchsine stain for pancreatic islet beta cells.[4]
- It has use as an Antischistosomal. [5]
Related compounds
References
- ↑ Thomas Gessner and Udo Mayer "Triarylmethane and Diarylmethane Dyes" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim.doi:10.1002/14356007.a27_179
- ↑ Horobin RW, Kiernan JA (2002) Conn's Biological Stains, 10th ed. Oxford: BIOS.
- ↑ J. B. Pate, J. P. Lodge, A. F. Wartburg (1962). "Effect of Pararosaniline in the Trace Determination of Sulfur Dioxide.". Analytical Chemistry 34 (12): 1660–1662. doi:10.1021/ac60192a001. ISSN 0003-2700. https://pubs.acs.org/doi/abs/10.1021/ac60192a001. Retrieved 2023-03-03.
- ↑ Mowry, RW; Emmel, VM (1978). "Aldehyde fuchsin staining, direct or after oxidation: problems and remedies, with special reference to pancreatic B cells, pituitaries and elastic fibers". Stain Technology 53 (3): 141–154. doi:10.3109/10520297809111457. PMID 83035.
- ↑ "Pharmaceutical compositions containing pararosaniline or derivatives thereof" GB patent 908634, published 1962-10-24
Further reading
- Colour Index 3rd Edition Volume 4, Bradford: Society of Dyers and Colourists, 1971, pp. 4388, http://www.colour-index.org/help/3121_Triarylmethane.pdf.
- Gessner, T.; Mayer, U. (2002), "Triarylmethane and Diarylmethane Dyes", Ullmann's Encyclopedia of Industrial Chemistry 6th Edition, Weinheim: Wiley-VCH, doi:10.1002/14356007.a27_179.
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