Summary
Millon's reagent is an analytical reagent used to detect the presence of soluble proteins. A few drops of the reagent are added to the test solution, which is then heated gently. A reddish-brown coloration or precipitate indicates the presence of tyrosine residue which occur in nearly all proteins.[1] The test was developed by the French chemist Auguste Nicolas Eugene Millon. The structure of the metal complex is usually misrepresented. It is an nitroso complex, with M-N bonds.[2]
The reagent is made by dissolving metallic mercury in nitric acid and diluting with water, forming mercuric nitrate (Hg[NO3]2).[3] In the test, the phenol group in the side chain of tyrosine gets nitrated, and that product then complexes with Hg(I) or Hg(II) ions to give a red colored precipitate. Millon's test is not specific for proteins; it also gives a positive test for other compounds containing the phenol functional group. Therefore, the biuret test or the ninhydrin reaction are used along with it to confirm the presence of proteins.
See also
editReferences
edit- ^ Walsh, Edward O. (1961). An Introduction to Biochemistry. London: The English Universities Press; Hodder & Stoughton. pp. 406–407. OCLC 421450365. Archived from the original on 2022-05-16. Retrieved 2022-05-16.
- ^ Kobayashi, Yoshiko; Iitaka, Yoichi; Kido, Yasumasa (1970). "The Crystal Structure of a Colored Complex, C7H7OHg·C7H6O2N, Obtained in the Millon Reaction of p -Cresol". Bulletin of the Chemical Society of Japan. 43 (10): 3070–3078. doi:10.1246/bcsj.43.3070.
- ^ "Millon's reagent, for the detection of Tyrosine, Thermo Scientific | Fisher Scientific". www.fishersci.com. Archived from the original on 16 May 2022. Retrieved 16 May 2022.