Structure Sucrose's
IUPAC name is
β-D-fructofuranosyl-(2→1)-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 Pure crystalline sucrose melts at approximately . However, the melting point is highly sensitive to the presence of water and impurities such as mineral salts, and sucrose also begins to decompose at a lower temperature than its melting point. The decomposition of sucrose is exploited in cookery to form
caramel. Like other
carbohydrates, sucrose 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.
Hydrolysis 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
(higher) 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 (UDP). 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 (589 nm) 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 (symbol °Bx), 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. == Sources ==