187112-40-9

Basic information

• Product Name: Basic Red 9
• Synonyms: 4-((4-Aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)phenylamine; 4,4'-[(4-Iminocyclohexa-2,5-dien-1-ylidene)methylene]dianiline; Benzenamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-; benzenamine, 4,4'-[(4-imino-2,5-cyclohexadien-1-ylidene)methylene]bis-; Benzenamine, 4-[(4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl]-; 4,4'-[(4-iminocyclohexa-2,5-dien-1-ylidene)methanediyl]dianiline; 4,4'-[(4-iminocyclohexa-2,5-dien-1-ylidene)methanediyl]dianiline nitrate (1:1); 4,4'-[(4-iminocyclohexa-2,5-dien-1-ylidene)methanediyl]dianiline acetate (1:1)
• CAS NO: 187112-40-9
• Molecular Formula: C₂₁H₂₁N₃O₂
• Molecular Weight: 347.4103
• EINECS: 262-806-0
• Mol File: 187112-40-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 568.2°C at 760 mmHg
• Flash Point: 297.4°C
• Vapor Pressure: 6.33E-13mmHg at 25°C
• CAS DataBase Reference: Basic Red 9(CAS DataBase Reference)
• NIST Chemistry Reference: Basic Red 9(187112-40-9)
• EPA Substance Registry System: Basic Red 9(187112-40-9)

Safety Data

• Hazardous Substances Data: 187112-40-9(Hazardous Substances Data)

Upstream product

• 467-62-9 pararosaniline 
• 16097-08-8 pararosaniline leucosulfonic acid 
• 569-61-9 C₁₉H₁₇N₃*2ClH 
• 548-62-9 crystal violet 
• 101-77-9 4,4'-diamino diphenyl methane 
• 62-53-3 aniline 
• 569-61-9 basic red 9 
• 569-61-9 C₁₉H₁₇N₃*3ClH 

Downstream Products

• 873664-04-1 C₃₁H₂₆N₃O₂P 
• 128527-15-1 4,4',4''-Tris(4-hydroxyphenylazo)triphenylmethanol 
• 128527-11-7 4,4',4''-Tris<4-(dimethylamino)phenylazo>triphenylmethanol 

Relevant articles and documents

Temperature Dependence of the Modified Pararosaniline Method for the Determination of Formaldehyde in Air

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A series of BiO: XIy/GO photocatalysts: Synthesis, characterization, activity, and mechanism

A series of bismuth oxyiodide (BiOxIy)-grafted graphene oxide (GO) sheets with different GO contents were synthesized through a simple hydrothermal method. This is the first report where four composites of BiOI/GO, Bi4O5I2/GO, Bi7O9I3/GO, and Bi5O7I/GO have been characterized using X-ray diffraction, transmission electron microscopy, scanning electron microscopy energy-dispersive spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The assembled BiOxIy/GO composites exhibited excellent photocatalytic activities in the degradation of crystal violet (CV) under visible light irradiation. The order of rate constants was as follows: Bi7O9I3/GO > Bi4O5I2/GO > Bi4O5I2 > Bi7O9I3 > Bi5O7I/GO > BiOI/GO > BiOI > Bi5O7I > GO. The photocatalytic activity of the Bi7O9I3/GO (or Bi4O5I2/GO) composite reached a maximum rate constant of 0.351 (or 0.322) h-1, which was 1.8 (or 1.7) times higher than that of Bi7O9I3 (or Bi4O5I2), 6-7 times higher than that of BiOI/GO, and 119-130 times higher than that of BiOI. The quenching effects of different scavengers and electron paramagnetic resonance demonstrated that the superoxide radical (O2-) played a major role and holes (h+) and hydroxyl radicals (OH) played a minor role as active species in the degradation of crystal violet (CV) and salicylic acid (SA). Possible photodegradation mechanisms are proposed and discussed in this research.

The structure of Schiff reagent aldehyde adducts and the mechanism of the Schiff reaction as determined by nuclear magnetic resonance spectroscopy

An nmr study of compounds isolated from the Schiff aldehyde reaction between pararosaniline hydrochloride , sulfur dioxide, and acetaldehyde has demonstrated that these adducts are α-anilinoalkylsulfonic acids.The evidence is incompatible with the other structures most often accepted in the literature, N-phenyl alkylsulfonamides.In combination with nmr spectra obtained from solutions of the Schiff reagent and the Schiff reaction and with literature spectrophotometric data, this result leads to a reasonable proposal for the mechanism of the colour development.The effects of the concentrations of the dye, acetaldehyde, and in particular, sulfur dioxide are explained and suggest that the dominant coloured species is a 2:1 acetaldehyde-dye adduct.The nmr results also reveal a kinetic/thermodynamic competition for acetaldehyde between the aniline of the dye and the aldehyde carbonyl leading to bisulfite addition.The relation of the Schiff test with acetaldehyde and the Feulgen test for aldehydes in biological samples is also discussed.