because it is a locating agent that identify the different substances , espically the invisible amine acid
Since amino acids are colourless compounds, ninhydrin is used for detecting them. To identify this, after development, the TLC plate is sprayed with ninhydrin reagent and dried in an oven, at 105°C for about 5 minutes. Ninhydrin reacts with α- amino acids that results in purple coloured spots [(due to the formation of the complex - Rheuman's purple).
Ninhydrin is used as a visualization reagent in thin layer chromatography to detect amino acids and other compounds that contain primary amines. When sprayed onto the developed TLC plate and heated, ninhydrin reacts with primary amines to form colored products, allowing for visualization and identification of the separated compounds.
Ninhydrin solution reacts with amino acids in the developed spots, producing a purple color. This color change makes the spots more visible and helps in their visualization on chromatography materials.
These are the amino acids that will yield positive result to the ninhydrin test: Non-polar amino acids: Glycine, Alanine, Valine, Leucine, Isoleucine, Phenylalanine, Methionine, Tryptophan Polar Neutral Amino acids: Serine, Cysteine, Threonine, Asparagine, Glutamine, Tyrosine Polar Acidic Amino Acids: Aspartic acid and Glutamic acid Polar Basic Amino Acids: Histidine, Lysine, Arginine
The boiling point of ninhydrin is approximately 275-280°C.
Since amino acids are colourless compounds, ninhydrin is used for detecting them. To identify this, after development, the TLC plate is sprayed with ninhydrin reagent and dried in an oven, at 105°C for about 5 minutes. Ninhydrin reacts with α- amino acids that results in purple coloured spots [(due to the formation of the complex - Rheuman's purple).
ninhydrin reagent
Ninhydrin is used as a visualization reagent in thin layer chromatography to detect amino acids and other compounds that contain primary amines. When sprayed onto the developed TLC plate and heated, ninhydrin reacts with primary amines to form colored products, allowing for visualization and identification of the separated compounds.
Ninhydrin is used as a TLC stain in chromatography experiments to detect and visualize amino acids and other compounds that contain primary amines. It reacts with these compounds to form a colored product, making it easier to identify and analyze them on the chromatogram.
Ninhydrin solution reacts with amino acids in the developed spots, producing a purple color. This color change makes the spots more visible and helps in their visualization on chromatography materials.
The locating agents commonly used in paper chromatography are ninhydrin, iodine vapor, and UV light. These agents help visualize the separated components on the paper chromatogram.
Proline can be estimated using spectrophotometric methods such as the ninhydrin method, which involves reacting proline with ninhydrin to form a colored product that can be measured at a specific wavelength. Another approach is using high-performance liquid chromatography (HPLC) to separate and quantify proline in a sample based on its unique retention time. Both techniques are commonly used for proline estimation in biological samples.
Ruhemann's purple is a deep violet compound that forms as a result of the reaction of ninhydrin with amino acids present in a sample. This color change is used in analytical techniques such as chromatography to detect and quantify amino acids. Ruhemann's purple formation indicates the presence of primary amines in the sample.
Ninhydrin is used in amino acid TLC because it readily stains amino acids by reacting with the amine groups. This reaction takes place very quickly and creates a brownish-color that can be easily visualized.
It really depends on the type of chromatography. E.g. with thin layer chromatography, UV light is used, and the amount of light that is absorbed is measured, and they can tell the amino acid from this. In paper chromatography, a substance called ninhydrin is sprayed onto the separated amino acids and they become visible.
Well, the best I could come up with is it's either:C9H6O2orC4H3O2If someone knows any different please correct me.jman63: it is actually C9H6O4
Yes, ninhydrin has some drawbacks. It can react with other substances present in the sample, leading to false positive results. Additionally, the reaction with ninhydrin is not specific to a particular amino acid, which can limit its application in identifying specific amino acids.