Sucrose
Sucrose is a disaccharide, a sugar composed of glucose and fructose subunits. It is produced naturally in plants and is the main constituent of white sugar. It has the molecular formula.
For human consumption, sucrose is extracted and refined from either sugarcane or sugar beet. Sugar mills – typically located in tropical regions near where sugarcane is grown – crush the cane and produce raw sugar which is shipped to other factories for refining into pure sucrose. Sugar beet factories are located in temperate climates where the beet is grown, and process the beets directly into refined sugar. The sugar-refining process involves washing the raw sugar crystals before dissolving them into a sugar syrup which is filtered and then passed over carbon to remove any residual colour. The sugar syrup is then concentrated by boiling under a vacuum and crystallized as the final purification process to produce crystals of pure sucrose that are clear, odorless, and sweet.
Sugar is often an added ingredient in food production and recipes. About 185 million tonnes of sugar were produced worldwide in 2017.
Etymology
The word sucrose was coined in 1857, by the English chemist William Miller from the French sucre and the generic chemical suffix for sugars -ose. The abbreviated term Suc is often used for sucrose in scientific literature.The name saccharose was coined in 1860 by the French chemist Marcellin Berthelot. Saccharose is an obsolete name for sugars in general, especially sucrose.
Physical and chemical properties
Structure
Sucrose's IUPAC name is β-D-fructofuranosyl--α-D-glucopyranoside. In this disaccharide, glucose and fructose are linked via a glycosidic linkage, i.e. an ether bond between C1 on the glucosyl subunit and C2 on the fructosyl unit. Glucose exists predominantly as a mixture of α and β "pyranose" anomers, but sucrose has only the α form. Fructose exists as a mixture of five tautomers but sucrose has only the β-D-fructofuranose form. Unlike most disaccharides, the glycosidic bond in sucrose is formed between the reducing ends of both glucose and fructose, and not between the reducing end of one and the non-reducing end of the other. This linkage inhibits further bonding to other saccharide units, and prevents sucrose from spontaneously reacting with cellular and circulatory macromolecules in the manner that glucose and other reducing sugars do. Since sucrose contains no anomeric hydroxyl groups, it is classified as a non-reducing sugar.Sucrose crystallizes in the monoclinic space group P21 with room-temperature lattice parameters a = 1.08631 nm, b = 0.87044 nm, c = 0.77624 nm, β = 102.938°.
Thermal and oxidative degradation
Sucrose does not melt at high temperatures. Instead, it decomposes at to form caramel. Like other carbohydrates, it combusts to carbon dioxide and water by the simplified equation:Mixing sucrose with the oxidizer potassium nitrate produces a fuel called rocket candy that is often used to propel amateur rocket motors.
This reaction is somewhat simplified though. Some of the carbon does get fully oxidized to carbon dioxide, and other reactions, such as the water-gas shift reaction also take place. A more accurate theoretical equation is:
Sucrose burns with chloric acid, formed by the reaction of hydrochloric acid and potassium chlorate:
Sucrose can be dehydrated with concentrated sulfuric acid to form a black, carbon-rich solid, as indicated in the following idealized equation:
The formula for sucrose's decomposition can be represented as a two-step reaction: the first simplified reaction is dehydration of sucrose to pure carbon and water, and then carbon is oxidised to by from air.
| T | S |
| 50 | 259 |
| 55 | 273 |
| 60 | 289 |
| 65 | 306 |
| 70 | 325 |
| 75 | 346 |
| 80 | 369 |
| 85 | 394 |
| 90 | 420 |
Hydrolysis
breaks the glycosidic bond converting sucrose into glucose and fructose. Hydrolysis is, however, so slow that solutions of sucrose can sit for years with negligible change. If the enzyme sucrase is added, however, the reaction will proceed rapidly. Hydrolysis can also be accelerated with acids, such as cream of tartar or lemon juice, both weak acids. Likewise, gastric acidity converts sucrose to glucose and fructose during digestion, the bond between them being an acetal bond which can be broken by an acid.Given heats of combustion of 1349.6 kcal/mol for sucrose, 673.0 for glucose, and 675.6 for fructose, hydrolysis releases about per mole of sucrose, or about 3 small calories per gram of product.
Synthesis and biosynthesis of sucrose
The biosynthesis of sucrose proceeds via the precursors UDP-glucose and fructose 6-phosphate, catalyzed by the enzyme sucrose-6-phosphate synthase. The energy for the reaction is gained by the cleavage of uridine diphosphate.Sucrose is formed by plants, algae and cyanobacteria but not by other organisms. Sucrose is the end product of photosynthesis and is found naturally in many food plants along with the monosaccharide fructose. In many fruits, such as pineapple and apricot, sucrose is the main sugar. In others, such as grapes and pears, fructose is the main sugar.
Chemical synthesis
After numerous unsuccessful attempts by others, Raymond Lemieux and George Huber succeeded in synthesizing sucrose from acetylated glucose and fructose in 1953.Measurement
The purity of sucrose is measured by polarimetry, i.e., the rotation of plane-polarized light by a sugar solution. The specific rotation at using yellow "sodium-D" light is +66.47°. Commercial samples of sugar are assayed using this parameter. Sucrose does not deteriorate at ambient conditions.The sugar industry uses degrees Brix, introduced by Adolf Brix, as units of measurement of the mass ratio of dissolved substance to water in a liquid. A 25 °Bx sucrose solution has 25 grams of sucrose per 100 grams of liquid; or, to put it another way, 25 grams of sucrose sugar and 75 grams of water exist in the 100 grams of solution. A 25 °Bx solution therefore has a concentration of 25 mass % sucrose.
Production
Table sugar comes from plant sources. Two important sugar crops predominate: sugarcane and sugar beets, in which sugar can account for 12% to 20% of the plant's dry weight. The plant material is separated to isolate the sucrose-rich portions. Purification of the sucrose exploits the good solubility of sucrose in water. After this aqueous extraction, a variety of tools and techniques allow further purification and production of solid forms suited for the markets.Culinary sugars
Mill white
Mill white, also called plantation white, crystal sugar or superior sugar is produced from raw sugar. It is exposed to sulfur dioxide during the production to reduce the concentration of color compounds and helps prevent further color development during the crystallization process. Although common to sugarcane-growing areas, this product does not store or ship well. After a few weeks, its impurities tend to promote discoloration and clumping; therefore this type of sugar is generally limited to local consumption.Blanco directo
Blanco directo, a white sugar common in India and other south Asian countries, is produced by precipitating many impurities out of cane juice using phosphoric acid and calcium hydroxide, similar to the carbonatation technique used in beet sugar refining. Blanco directo is purer than mill white sugar, but less pure than white refined sugar.White refined
White sugar, also called table sugar or regular sugar, is a commonly used type of sugar, made either of beet sugar or cane sugar. It is nearly pure sucrose. The refining process completely removes the molasses from cane juice or beet juice to give the disaccharide white sugar, sucrose. It has a purity higher than 99.7%. Its molecular formula is. White sugars produced from sugar cane and sugar beet are chemically indistinguishable: it is possible, however, to identify their origin through a carbon-13 analysis.From a chemical and nutritional point of view, white sugar does not contain minerals present in small quantities in molasses. The only detectable differences are, therefore, the white color and the less intense flavor.
White refined sugar is typically sold as granulated sugar, which has been dried to prevent clumping and comes in various crystal sizes for home and industrial use:
Image:Sucre blanc cassonade complet rapadura.jpg|thumb|Sugars; clockwise from top left: Refined, unrefined, brown, unprocessed cane
- Coarse-grain, such as sanding sugar is a coarse grain sugar used to add sparkle and flavor atop baked goods and candies. Its large reflective crystals will not dissolve when subjected to heat.
- Granulated, familiar as table sugar, with a grain size about 0.5 mm across. "Sugar cubes" are lumps for convenient consumption produced by mixing granulated sugar with sugar syrup.
- Caster, a fine white sugar with small grains favorable for cooking. Commonly used in baking and mixed drinks, it is sold as "superfine" sugar in the United States. Because of its fineness, it dissolves faster than regular white sugar and is especially useful in meringues and cold liquids. Caster sugar can be prepared at home by grinding granulated sugar for a couple of minutes in a mortar or food processor.
- Powdered, confectioner's sugar, or icing sugar, produced by grinding sugar to a fine powder. The manufacturer may add a small amount of anticaking agent to prevent clumping — either corn starch or tricalcium phosphate.