Benedict's reagent
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|
 Positive Benedict's test | |
| Classification | Colorimetric method |
|---|---|
| Analytes | Reducing sugars |
Benedict's reagent (often called Benedict's qualitative solution or Benedict's solution) is a chemical reagent and complex mixture of sodium carbonate, sodium citrate and copper(II) sulphate pentahydrate.[1], often used in place of Fehling's solution to detect the presence of reducing sugars. The presence of other reducing substances also gives a positive reaction.[2] Such tests that use this reagent are called the Benedict's tests. A positive test with Benedict's reagent is shown by a color change from clear blue to a brick-red precipitate.
Generally, Benedict's test detects the presence of aldehydes and alpha-hydroxy-ketones, also by hemiacetal, including those that occur in certain ketoses. Thus, although the ketose fructose is not strictly a reducing sugar, it is an alpha-hydroxy-ketone, and gives a positive test because it is converted to the aldoses glucose and mannose by the base in the reagent.
The principle of Benedict's test is that when reducing sugars are heated in the presence of an alkali they are converted to powerful reducing species known as enediols. Enediols reduce the cupric compounds (Cu2+) present in the Benedict's reagent to cuprous compounds (Cu+) which are precipitated as insoluble red copper(I) oxide(Cu2O).
The color of the obtained precipitate gives an idea about the quantity of sugar present in the solution, hence the test is semi-quantitative. A greenish precipitate indicates about 0.5 g% concentration; yellow precipitate indicates 1 g% concentration; orange indicates 1.5 g% and red indicates 2 g% or higher concentration.
Benedict's test for organic analysis
To test for the presence of monosaccharides and reducing disaccharide sugars in food, the food sample is dissolved in water, and a small amount of Benedict's reagent is added. During a water bath, which is usually 4–10 minutes, the solution should progress in the colors of blue (with no reducing sugar present), orange, yellow, green, red, and then brick red precipitate or brown (with high reducing sugar present). A color change would signify the presence of a reducing sugar.[2] The common disaccharides lactose and maltose are directly detected by Benedict's reagent because each contains a glucose with a free reducing aldehyde moiety (functional group), after isomerization.
Sucrose (table sugar) contains two sugars (fructose and glucose) joined by their glycosidic bond in such a way as to prevent the glucose isomerizing to aldehyde, or the fructose to alpha-hydroxy-ketone form. Sucrose is thus a non-reducing sugar which does not react with Benedict's reagent. Sucrose indirectly produces a positive result with Benedict's reagent if heated with dilute hydrochloric acid prior to the test, although after this treatment it is no longer sucrose. The acidic conditions and heat break the glycosidic bond in sucrose through hydrolysis. The products of sucrose decomposition are glucose and fructose, both of which can be detected by Benedict's reagent, as described above.
Starches do not react or react very poorly with Benedict's reagent, due to the relatively small number of reducing sugar moieties, which occur only at the ends of carbohydrate chains. Inositol (myoinositol) is another carbohydrate which produces a negative test.
Benedict's reagent can be used to test for the presence of glucose in urine. Glucose in urine is called glucosuria and can be indicative of diabetes mellitus, but the test is not recommended or used for the diagnosis of diabetes mellitus. A false positive reaction can be due to the presence of other reducing substances in urine such as ascorbic acid (during intake of vitamin supplements), drugs (levodopa, contrast used in radiological procedures) and homogentisic acid (alkaptonuria).
Benedict's solution
Benedict's solution is a deep-blue solution used to test for the presence of the aldehyde functional group, - CHO.[2] It is an aqueous alkaline mixture of CuSO4 and sodium citrate. Here sodium citrate is the complexing agent that keeps Cu2+ in solution, which would otherwise precipitate as cupric carbonate. The substance to be tested is heated up to 95 °C (for example, in a water bath) with Benedict's solution; formation of a brick-red precipitate indicates presence of the aldehyde group in relatively high concentrations.[2] Since simple sugars (e.g., glucose) give a positive test, the solution is used to test for the presence of glucose in urine, a sign of diabetes. One litre of Benedict's solution contains 173 grammes sodium citrate, 100 grammes sodium carbonate, and 17.3 grammes cupric sulphate pentahydrate. It reacts chemically similarly to Fehling's solution; the cupric ion (complexed with citrate ions) is reduced to cuprous ion by the aldehyde group (which is oxidised), and precipitates as cuprous oxide, Cu2O.
| Experiment | Observation | Inference |
|---|---|---|
| Substance in water + 3ml Benedict's solution, then boil for few minutes and allow to cool. | Red, green, or yellow precipitate is obtained | Reducing sugar e.g. Glucose is present |
| Substance in water + 3ml Benedict's solution, then boil for few minutes and allow to cool. | Solution remains clear or is a little blue | Reducing sugar is not present |
Benedict's reagent: It can be used to test for the presence of glucose in urine. Glucose in urine is called glucosuria and can be indicative of diabetes mellitus, but the test is not recommended or used for the diagnosis of diabetes mellitus. A false positive reaction can be due to the presence of other reducing substances in urine such as ascorbic acid (during intake of vitamin supplements), drugs (levodopa, contrast used in radiological procedures) and homogentisic acid (alkaptonuria).
Preparation of Benedict's reagent: Dissolve 173 g of sodium citrate and 100 g of anhydrous sodium carbonate in 800 ml of slightly warm distilled water. Filter it, if necessary. Dissolve 17.3 g of copper sulphate (cupric sulphate) in 100 ml of distilled water separately. Mix this copper sulphate solution slowly with 800 ml of sodium carbonate-citrate solution with constant stirring. Now make the final volume 1000 ml with distilled water.(Ref: Chapter 48 in Essentials of Practical Biochemistry, Prem Prakash & Neelu Gupta, Jaypee Brothers Medical Publishers, Ltd)
Quantitative reagent
Benedict's quantitative reagent contains potassium thiocyanate and is used to determine how much reducing sugar is present.[2] This solution forms a copper thiocyanate precipitate which is white and can be used in a titration. The titration should be repeated with 1% glucose solution instead of the sample for calibration.
Benedict refers to American chemist Stanley Rossiter Benedict.[3]
See also
Other oxidizing reagents
Other reducing reagents (opposite)
References
- ^ Robert D. Simoni; Robert L. Hill; Martha Vaughan (2002). "Benedict's Solution, a Reagent for Measuring Reducing Sugars: the Clinical Chemistry of Stanley R. Benedict". J. Biol. Chem. 277 (16): 10–11. doi:10.1074/jbc.M110516200. PMC 4492735. PMID 11773074.
{{cite journal}}: Unknown parameter|last-author-amp=ignored (|name-list-style=suggested) (help)CS1 maint: unflagged free DOI (link) - ^ a b c d e Collins Edexcel International GCSEBiology, Student Book (ISBN 978-0-00-745000-8) p.42-43
- ^ Benedict, S. R.7 (1 January 1909). "A Reagent For the Detection of Reducing Sugars" (PDF). J. Biol. Chem. 5 (6): 485–487.
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