2152-98-9 , b1-4Galactobiose; Galb1-4Gal , 4-O-(b-D-Galactopyranosyl)-D-galactopyranose
C12H22O11 / 342.29
Beta-D-galactopyranosyl-(1->4)-D-galactopyranose, also known as lactose, is a disaccharide composed of galactose and glucose. It is found in milk and dairy products and is widely used as a sweetener, filler, and bulking agent in the food industry. In this paper, we will explore the various aspects of beta-D-galactopyranosyl-(1->4)-D-galactopyranose, including its definition and background, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.
Definition and Background
Beta-D-galactopyranosyl-(1->4)-D-galactopyranose is a disaccharide made up of beta-D-galactose and alpha-D-glucose. It is also known as lactose, and it is found in milk and dairy products. Lactose makes up around 2-8% of the milk of mammals, depending on the species. Human milk has a lower lactose content than that of cows and other domesticated animals. The name lactose comes from the Latin word “lac,” which means milk.
Physical and Chemical Properties
Beta-D-galactopyranosyl-(1->4)-D-galactopyranose is a white, crystalline, odorless powder with a sweet taste. It is soluble in water and practically insoluble in alcohol, ether, and chloroform. The molecular weight of lactose is 342.3 g/mol, and its melting point is 202°C.
Synthesis and Characterization
Lactose can be synthesized chemically or enzymatically. In the chemical synthesis, galactose and glucose are condensed by heating in the presence of an acid catalyst. The resulting lactose is then purified by crystallization. Enzymatic synthesis, on the other hand, involves the use of beta-galactosidase, which catalyzes the condensation of galactose and glucose. The resulting lactose is then purified by chromatography or crystallization.
Analytical Methods
Several analytical methods can be used to quantify lactose in various samples. Among them, HPLC and TLC are widely used methods. In HPLC, the lactose is separated from other components of the sample by a column, and its concentration is measured by detecting the absorbance at a specific wavelength. TLC, on the other hand, separates the components of the sample in a thin layer of silica gel or aluminum oxide, and the lactose can be detected by spraying with a reagent that reacts with it.
Biological Properties
Beta-D-galactopyranosyl-(1->4)-D-galactopyranose is an important source of energy for infants and adults. It is hydrolyzed in the small intestine by lactase, an enzyme produced by the brush border of the small intestine. The resulting glucose and galactose are then absorbed into the bloodstream and used as a source of energy. People with lactose intolerance have a deficiency of lactase, which leads to the accumulation of undigested lactose in the large intestine, causing symptoms such as abdominal pain, bloating, and diarrhea.
Toxicity and Safety in Scientific Experiments
Lactose is generally regarded as safe and non-toxic in scientific experiments. However, it can cause allergic reactions in some people, especially those who are allergic to milk.
Applications in Scientific Experiments
Beta-D-galactopyranosyl-(1->4)-D-galactopyranose is a widely used substrate in enzymatic assays for the detection and quantification of lactase activity. It is also used as a source of carbon and energy in the culture media for the growth of bacteria and yeast.
Current State of Research
Research on beta-D-galactopyranosyl-(1->4)-D-galactopyranose is ongoing in various fields. In the food industry, lactose is used as a sweetener, filler, and bulking agent. In the pharmaceutical industry, lactose is used as an excipient in the formulation of tablets and capsules.
Potential Implications in Various Fields of Research and Industry
Lactose has potential implications in various fields of research and industry. In the food industry, lactose-free products are becoming increasingly popular due to the growing number of people with lactose intolerance. In the pharmaceutical industry, the use of lactose-free excipients is being explored to improve the bioavailability of drugs.
Limitations
One limitation of lactose is its low solubility in organic solvents, which limits its applications in some fields. Another limitation is its potential to cause allergic reactions in some people, which restricts its use in certain products.
Future Directions
There are several future directions for research on beta-D-galactopyranosyl-(1->4)-D-galactopyranose. One direction is the development of new synthetic methods for lactose that are more efficient and environmentally friendly. Another direction is the exploration of lactose-free excipients for the formulation of drugs. Moreover, the use of lactose in the development of new biomaterials, such as hydrogels and nanoparticles, is also an area of interest. Finally, the investigation of the potential health benefits of lactose, such as its prebiotic properties, is an area that needs further research.
CAS Number | 2152-98-9 |
Product Name | beta-D-galactopyranosyl-(1->4)-D-galactopyranose |
IUPAC Name | (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3R,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol |
Molecular Formula | C12H22O11 |
Molecular Weight | 342.3 g/mol |
InChI | InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5+,6+,7-,8-,9-,10+,11?,12+/m1/s1 |
InChI Key | GUBGYTABKSRVRQ-HEJLOQJISA-N |
SMILES | C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O |
Canonical SMILES | C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O |
Isomeric SMILES | C([C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@H]2[C@H](OC([C@@H]([C@H]2O)O)O)CO)O)O)O)O |
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