aniline hydrofluoride. It becomes magenta when dissolved in water; as a solid, it forms dark green crystals. Hunger K (2003) Industrial Dyes. ; [Cl-]. ", https://en.wikipedia.org/w/index.php?title=Fuchsine&oldid=972666227, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Articles with unsourced statements from September 2012, Wikipedia articles needing clarification from November 2012, Creative Commons Attribution-ShareAlike License. 2,4,6-Trichloroaniline is a chemical compound with a formula of C6H4Cl3N. Their structure differs from the structure shown above by the absence of the methyl group on the upper ring, otherwise they are quite similar. When warmed with aniline it yields anilido-aposafranine, which may also be obtained by the direct oxidation of ortho-aminodiphenylamine. aniline hydrochloride. Ingestion, inhalation, skin and eye contact, combustible at high temperature, slightly explosive around open flames and sparks. Wikipedia® est une marque déposée de la Wikimedia Foundation, Inc., organisation de bienfaisance régie par le paragraphe 501(c)(3) du code fiscal des États-Unis. Names IUPAC name. MDL number MFCD00012958. DSSTox_RID_75362. New Window. Help. This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. Basic fuchsine is a mixture of rosaniline, pararosaniline, new fuchsine and Magenta II. [4] It is well established that production of fuchsine results in development of bladder cancers by production workers. Basic fuchsine in aqueous solution. In solution with phenol (also called carbolic acid) as an accentuator[15] it is called carbol fuchsin and is used for the Ziehl–Neelsen and other similar acid-fast staining of the mycobacteria which cause tuberculosis, leprosy etc. [5], Fuchsine was first prepared by August Wilhelm von Hofmann from aniline and carbon tetrachloride in 1858. Phenylhydrazine forms monoclinic prisms that melt to an oil around room temperature which may turn yellow to dark red upon exposure to air. Original file ‎(SVG file, nominally 245 × 260 pixels, file size: 15 KB). Files are available under licenses specified on their description page. (T. [1] Induline consists of a mixture of several intensely colored species, so the name is often indulines. The indulines may be subdivided into the following groups: (1) benzindulines, derivatives of phenazine; (2) isorosindulines; and (3) rosindulines, both derived from naphthophenazine; and (4) naphthindulines, derived from naphthazine. NACRES NA.22 [16] Basic fuchsine is widely used in biology to stain the nucleus, and is also a component of Lactofuchsin, used for Lactofuchsin mounting. [1], The rosindulines and naphthindulines have a strongly basic character, and their salts possess a marked red color and fluorescence. New Window. This page was last edited on 13 August 2020, at 07:43. It is sparingly soluble in water. Chemistry, Properties, Applications. 2.4.1 MeSH Entry Terms. 4-METHOXYBENZENAMINE HYDROCHLORIDE. aniline diphosphate (1:1) aniline diphosphate (3:1) aniline diphosphate (4:1) aniline hydrobromide. Compare Products: Select up to 4 products. [3] American and English dictionaries (Webster's, Oxford, Chambers, etc.) Consisting of a phenyl group attached to an amino group, aniline is the prototypical aromatic amine. Pubchem - ANILINE HYDROCHLORIDE; Wikipedia - Anilinium chloride. Fuchsine is an amine salt and has three amine groups, two primary amines and a secondary amine. HCl. HCl. The crystals pictured at the right are of basic fuchsine, also known as basic violet 14, basic red 9, pararosanaline or CI 42500. [NH2+]=C\1/C=C\C(C=C/1)=C(\c2ccc(N)c(C)c2)c3ccc(N)cc3, Except where otherwise noted, data are given for materials in their. COVID-19 is an emerging, rapidly evolving situation. There are other similar chemical formulations of products sold as fuchsine, and several dozen other synonyms of this molecule. This page was last edited on 21 September 2020, at 20:18. In the literature of biological stains the name of this dye is frequently misspelled, with omission of the terminal -e, which indicates an amine. p-Anisidine hydrochloride, 99%.

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