Methyl orange
Template:ChemboxTemplate:Infobox color Methyl orange is a pH indicator frequently used in titration because of its clear and distinct color variance at different pH values. Methyl orange shows red color in acidic medium and yellow color in basic medium. Because it changes color at the pKa of a mid strength acid, it is usually used in titration of strong acids in weak bases that reach the equivalence point at a pH of 3.1-4.4.<ref name="A/B Indicators">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Unlike a universal indicator, methyl orange does not have a full spectrum of color change, but it has a sharp end point. In a solution becoming less acidic, methyl orange changes from red to orange and, finally, to yellow—with the reverse process occurring in a solution of increasing acidity.
Indicator colorsEdit
In a solution that decreases in acidity, methyl orange moves from the color red to orange and finally to yellow with the opposite occurring for a solution increasing in acidity. This color change from yellow to red occurs because the protons in the acidic solution react with the N=N bond of the molecule, protonating one of them and changing the visible light absorption of the molecule to reflect more red light than orange/yellow. Template:PH indicator template In an acid, it is reddish and in alkali, it is yellow. Methyl orange has a pKa of 3.47 in water at Template:Convert.<ref>Template:Cite journal</ref>
Other indicatorsEdit
{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Template:PH indicator template Modified (or screened) methyl orange, an indicator consisting of a solution of methyl orange and xylene cyanol, changes from grey-violet to green as the solution becomes more basic.
SafetyEdit
Methyl orange has mutagenic properties.<ref name=sciencelab>MSDS Template:Webarchive from ScienceLab.com, Inc. Retrieved 2011-09-24</ref> When methyl orange is put under oxidative stress, one of the double-bonded nitrogen atoms that connects the aromatic rings gets radicalized and can further break down into reactive oxygen species or anilines, which are carcinogenic and can mutate DNA.<ref name="Radiat. Phys. Chem.">Template:Cite journal</ref> Various bacteria and enzymes can also cause this breakdown to occur.
SynthesisEdit
Methyl orange is an azobenzene derivative that can be formed from dimethylaniline and sulfanilic acid, first through a diazonium salt formation with the sulfanilic acid, followed by a nucleophilic attack from the dimethylaniline and rearomatization.<ref>Template:Cite journal</ref>
UV-vis spectrumEdit
The absorption of methyl orange on the UV-vis spectrum is between 350-550 nm, with its peak at 464 nm. This is in the green-purple visible light range and explains why methyl orange is, in fact, orange.<ref>Template:Cite journal</ref>
See alsoEdit
- Bromothymol blue
- Congo red
- Litmus
- Methyl red
- pH indicator
- Phenolphthalein
- Sulfarsazene
- Universal indicator