Benedict's reagent

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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) sulfate pentahydrate.[1] It is 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 result.[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 brick-red with a precipitate.

Benedict's test
Trommer's test.jpg
Positive Benedict's test
ClassificationColorimetric method
AnalytesReducing sugars

Generally, Benedict's test detects the presence of aldehydes, alpha-hydroxy-ketones, and hemiacetals, 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. Oxidation of the reducing sugar by the cupric (Cu2+) complex of the reagent produces a cuprous (Cu+), which precipitates as insoluble red copper(I) oxide (Cu2O).[3]

It is named after American chemist Stanley Rossiter Benedict.[4]

Organic analysisEdit

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 through the colors of blue (with no reducing sugar present), orange, yellow, green, red, and then brick red precipitate or brown (if a high concentration of reducing sugar is present). A color change would signify the presence of a reducing sugar.[2]

Experiment Observation Inference
Substance in water + 3 mL Benedict's solution, then boil for few minutes and allow to cool. Red, green, or yellow precipitate is obtained Reducing sugar, such as glucose, is present
Substance in water + 3 mL 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

The common disaccharides lactose and maltose are directly detected by Benedict's reagent because each contains a glucose with a free reducing aldehyde moiety 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 undergoing isomerization to an aldehyde, or fructose to alpha-hydroxy-ketone form. Sucrose is thus a non-reducing sugar which does not react with Benedict's reagent. However, sucrose indirectly produces a positive result with Benedict's reagent if heated with dilute hydrochloric acid prior to the test, although it is modified during this treatment as 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. Other carbohydrates which produce a negative result include inositol.

Benedict's reagent can also be used to test for the presence of glucose in urine, elevated levels of which is known as glucosuria. Glucosuria can be indicative of diabetes mellitus, but Benedict's test is not recommended or used for diagnosis of the aforementioned condition. This is due to the possibility of a reaction in which the presence of other reducing substances such as ascorbic acid, drugs (levodopa, contrast used in radiological procedures) and homogentisic acid (alkaptonuria) creates a false positive.

As color of the obtained precipitate can be used to infer the quantity of sugar present in the solution, 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% concentration; and red indicates 2 g% or higher concentration.

Composition and preparationEdit

Benedict's solution is deep-blue.[2] It is an aqueous alkaline mixture of CuSO4 and sodium citrate.[5] Sodium citrate acts as a complexing agent which serves to keeps Cu2+ in solution, which would otherwise precipitate as cupric carbonate. Sodium carbonate serves to keep the solution alkaline. 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.

Quantitative reagentEdit

Benedict's quantitative reagent contains potassium thiocyanate and is used to quantitatively determine the concentration of reducing sugars.[2] This solution forms a copper thiocyanate precipitate which is white and can be used in titration. The titration should be repeated with 1% glucose solution instead of the sample for calibration.

Net reactionEdit

The net reaction between an aldehyde (or an alpha-hydroxy-ketone) and the copper(II) ions in Benedict's solution may be written as

RCHO + 2 Cu2+ + 5 OH → RCOO + Cu2O + 3 H2O.

The hydroxide ions in the equation forms when sodium carbonate dissolves in water. With the citrate included, the reaction becomes

RCHO + 2 Cu(C6H5O7) + 5 OH → RCOO + Cu2O + 2 C6H5O73− + 3 H2O.

See alsoEdit

Other oxidizing reagents

Other reducing reagents


  1. ^ 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.
  2. ^ a b c d Collins Edexcel International GCSEBiology, Student Book (ISBN 978-0-00-745000-8) p.42-43
  3. ^ "Carbohydrates - Benedict's Test". Retrieved 2020-03-08.
  4. ^ Benedict, S. R.7 (1 January 1909). "A Reagent For the Detection of Reducing Sugars" (PDF). J. Biol. Chem. 5 (6): 485–487.
  5. ^ Prakash, Prem; Gupta, Neelu. Essentials of Practical Biochemistry. Jaypee Brothers Medical Publishers. pp. Chapter 48.