28447-38-3 , b-D-Gal-(1→3)-D-Glc ,
3-O-(b-D-Galactopyranosyl)-D-glucopyranose
C12H22O11 / 342.30
MFCD15145334
3-O-(b-D-Galactopyranosyl)-D-glucopyranose
3-O-beta-D-Galactopyranosyl-D-glucopyranose or lactose, as commonly known, is a disaccharide sugar composed of galactose and glucose. It is found naturally in milk and dairy products. The sugar is widely used in food processing, pharmaceuticals, biotechnology, and other related industries. This paper reviews the definition, background, physical and chemical properties, synthesis, 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
3-O-beta-D-Galactopyranosyl-D-glucopyranose is a disaccharide sugar composed of galactose and glucose. It has a molecular formula of C12H22O11 and a molecular weight of 342.30 g/mol. The sugar is also known as lactose and is naturally found in mammalian milk, including cow's milk, goat's milk, and human milk. It is used as a primary energy source for infants and is important in maintaining bone density in adults.
Physical and Chemical Properties
3-O-beta-D-Galactopyranosyl-D-glucopyranose is a white, odorless, crystalline powder that is soluble in water but insoluble in ethanol, methanol, and ether. It has a melting point of 202-204°C and an alpha-D-galactose linkage at position three. The sugar has a reducing property and is a non-reducing sugar.
Synthesis and Characterization
3-O-beta-D-Galactopyranosyl-D-glucopyranose can be synthesized through several methods. The most common method is the acid hydrolysis of lactose from milk. The acid hydrolysis process involves heating the milk with hydrochloric acid, which breaks down the lactose into its constituent parts of glucose and galactose. Another method is the enzymatic hydrolysis of lactose using the enzyme beta-galactosidase. The enzyme hydrolyzes the lactose into glucose and galactose.
Characterization of 3-O-beta-D-Galactopyranosyl-D-glucopyranose is done using several techniques, including nuclear magnetic resonance (NMR), liquid chromatography-mass spectrometry (LC-MS), and Fourier transform infrared (FT-IR) spectroscopy.
Analytical Methods
The analytical methods for 3-O-beta-D-Galactopyranosyl-D-glucopyranose include chromatography, electrophoresis, and spectrophotometry. High-performance liquid chromatography (HPLC) is the most commonly used method for assessing the purity and quantity of lactose in samples.
Biological Properties
3-O-beta-D-Galactopyranosyl-D-glucopyranose is a source of energy for infants and plays a vital role in maintaining bone density in adults. Studies have shown that lactose can also enhance the absorption of calcium and magnesium in the body. The sugar has also been shown to have prebiotic effects, promoting the growth of beneficial bacteria in the gut.
Toxicity and Safety in Scientific Experiments
3-O-beta-D-Galactopyranosyl-D-glucopyranose has been deemed safe for human consumption by regulatory agencies, including the United States Food and Drug Administration (FDA). However, lactose intolerance is a common condition in which the body cannot digest lactose due to the lack of the enzyme lactase. The condition can cause digestive issues, including diarrhea, bloating, and abdominal pain.
Applications in Scientific Experiments
3-O-beta-D-Galactopyranosyl-D-glucopyranose is widely used in the food industry as a sweetening agent, stabilizer, and texturizer. It is also used in pharmaceuticals as an excipient and in biotechnology as a substrate for enzyme and microbial production. Lactose is also used as a nutrient in cell culture media and as a diluent in dry powder inhalers.
Current State of Research
Current research on 3-O-beta-D-Galactopyranosyl-D-glucopyranose is focused on its potential health benefits and applications in medical treatments. Studies have shown that lactose may improve calcium and magnesium absorption, reduce the risk of osteoporosis and colon cancer, and improve gut health. Lactose has also been investigated as a potential carrier for targeted drug delivery.
Potential Implications in Various Fields of Research and Industry
3-O-beta-D-Galactopyranosyl-D-glucopyranose has implications in various fields of research and industry, including food processing, pharmaceuticals, biotechnology, and medical treatments. Lactose-based drugs have the potential for targeted drug delivery, and lactose can be used as a prebiotic in functional foods. The sugar can also be used as a nutrient for microbial production and cell culture media.
Limitations and Future Directions
One limitation of lactose is its low solubility in ethanol, methanol, and ether, limiting its applications in some industries. Future research on lactose should focus on improving its solubility in these solvents and exploring its potential applications in medical treatments, functional foods, and biotechnology.
Conclusion
3-O-beta-D-Galactopyranosyl-D-glucopyranose or lactose is a disaccharide sugar composed of galactose and glucose. It is found naturally in mammalian milk and is widely used in various industries, including food processing, pharmaceuticals, and biotechnology. The sugar has potential health benefits and is safe for human consumption. Further research on lactose should focus on improving its solubility in solvents and exploring its potential applications in medical treatments, functional foods, and biotechnology.
CAS Number | 28447-38-3 |
Product Name | 3-O-beta-D-Galactopyranosyl-D-glucopyranose |
IUPAC Name | (3R,4S,5R,6R)-6-(hydroxymethyl)-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2,3,5-triol |
Molecular Formula | C12H22O11 |
Molecular Weight | 342.3 g/mol |
InChI | InChI=1S/C12H22O11/c13-1-3-5(15)7(17)8(18)12(22-3)23-10-6(16)4(2-14)21-11(20)9(10)19/h3-20H,1-2H2/t3-,4-,5+,6-,7+,8-,9-,10+,11?,12+/m1/s1 |
InChI Key | QIGJYVCQYDKYDW-SFOYIGFHSA-N |
SMILES | C(C1C(C(C(C(O1)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O |
Canonical SMILES | C(C1C(C(C(C(O1)O)O)OC2C(C(C(C(O2)CO)O)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]([C@H](OC([C@@H]2O)O)CO)O)O)O)O)O |
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