Skip to main content

Methyl Orange

Methyl orange is a pH indicator frequently used in titrations because of its clear and distinct colour change. Because it changes colour at the pH of a midstrength acid, it is usually used in titrations for acids. Unlike a universal indicator, methyl orange does not have a full spectrum of colour change, but has a sharper end point. Methyl orange shows red colour in acidic medium and yellow colour in basic medium.

In a solution becoming less acidic, methyl orange moves from red to orange and finally to yellow with the reverse occurring for a solution increasing in acidity.The entire color change occurs in acidic conditions.In an acid, it is reddish and in alkali, it is yellow. Methyl orange has a pKa of 3.47 in water at 25 °C (77 °F).
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.
Since acidic solutions have low pH values, it will be red and transition to orange and yellow as the acidity of the solution decreases. In basic solutions, it will be yellow as well as in neutral solutions because the pH of a neutral solution is approximately 7 and falls after the color change of methyl orange.

Dissolve 0.5 g of bromothymol blue in 500 mL of water. Add a drop of ammonia solution to turn the solution deep blue in colour. Prepare methyl orange acid-base indicator, pH < 3.1 red to pH > 4.4 yellow-orange. It is best for solutions with concentration > M/5.
pH-related color changes result from changes in the way electrons are confined in a molecule when hydrogen ions are attached or detached. Here is the structure of methyl orange in acidic solution: The molecule absorbs blue-green light, which makes its solution appear red.
Methyl orange is a pH indicator frequently used in titrations because of its clear and distinct colour change. Because it changes colour at the pH of a midstrength acid, it is usually used in titrations for acids.



Comments

Popular posts from this blog

Phenol-Formaldehyde Resin

Phenol formaldehyde resins (PF) or phenolic resins are synthetic polymers obtained by the reaction of phenol or substituted phenol with formaldehyde. Used as the basis for Bakelite, PFs were the first commercial synthetic resins (plastics). They have been widely used for the production of molded products including billiard balls, laboratory countertops, and as coatings and adhesives. They were at one time the primary material used for the production of circuit boards but have been largely replaced with epoxy resins and fiberglass cloth, as with fire-resistant FR-4 circuit board materials. There are two main production methods. One reacts phenol and formaldehyde directly to produce a thermosetting network polymer, while the other restricts the formaldehyde to produce a prepolymer known as novolac which can be moulded and then cured with the addition of more formaldehyde and heat. There are many variations in both production and input materials that are used to produce a wide variety...

Malachite Green Dye

Malachite green is an organic compound that is used as a dyestuff and controversially as an antimicrobial in aquaculture. Malachite green is traditionally used as a dye for materials such as silk, leather, and paper. Despite its name the dye is not prepared from the mineral malachite, and the name just comes from the similarity of color. Malachite green is classified in the dyestuff industry as a triarylmethane dye and also using in pigment industry. Formally, malachite green refers to the chloride salt [C6H5C(C6H4N(CH3)2)2]Cl, although the term malachite green is used loosely and often just refers to the colored cation. The oxalate salt is also marketed. The anions have no effect on the color. The intense green color of the cation results from a strong absorption band at 621 nm (extinction coefficient of 105 M−1 cm−1). Malachite green is prepared by the condensation of benzaldehyde and dimethylaniline to give leuco malachite green (LMG): C6H5CHO + 2 C6H5N(CH3)2 → C6H5CH(C6H4N...