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  • 35175-16-7 , 6-a-D-Glucopyranosyl maltotriose
35175-16-7 , 6-a-D-Glucopyranosyl maltotriose

35175-16-7 , 6-a-D-Glucopyranosyl maltotriose

35175-16-7 , 6-a-D-Glucopyranosyl maltotriose ,
Glc a1-6 Glc a1-4 Glc a1-4 Glc;
Glucose tetrasaccharide;
6''-a-D-Glucosyl-maltotriose;
Tetraglucoside;
O-a-D-Glucopyranosyl-(1,6)-O-a-D-glucopyranosyl-(1,4)-O-a-D-glucopyranosyl-(1,4)-D-glucose
C24H42O21 / 666.58
MFCD02179377

6-a-D-Glucopyranosyl maltotriose , Glc a1-6 Glc a1-4 Glc a1-4 Glc;

Glucose tetrasaccharide; 6''-a-D-Glucosyl-maltotriose; Tetraglucoside; 

O-a-D-Glucopyranosyl-(1,6)-O-a-D-glucopyranosyl-(1,4)-O-a-D-glucopyranosyl-(1,4)-D-glucose


Tetraglucoside, also known as gluco-oligosaccharide, is a complex sugar that is composed of four glucose units linked through glycosidic bonds. This compound has been the focus of much research due to its unique physical and chemical properties, as well as its potential applications in various industries, including food, cosmetics, and pharmaceuticals. In this paper, we will explore the 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, and limitations and future directions of tetraglucoside.

Definition and Background

Tetraglucoside is a type of oligosaccharide, a carbohydrate molecule made up of a small number of sugar units. It is commonly found in various natural sources, such as honey, corn syrup, and malt extract. Tetraglucoside is also produced through the partial hydrolysis of starch and cellulose.

Physical and Chemical Properties

Tetraglucoside is a white, crystalline powder that is soluble in water but insoluble in organic solvents. It has a sweet taste and a low caloric value, making it a suitable alternative to sugar in certain food products. The chemical formula for tetraglucoside is C24H42O21, and its molecular weight is 666.58 g/mol.

Synthesis and Characterization

Tetraglucoside can be synthesized through several methods, including enzymatic hydrolysis, acid hydrolysis, and transglycosylation. Enzymatic hydrolysis involves the use of enzymes such as amylase and cellulase to break down starch and cellulose into tetraglucoside. Acid hydrolysis involves the use of strong acids such as sulfuric acid to break down starch and cellulose.

Analytical Methods

Various analytical methods can be used to determine the purity and composition of tetraglucoside. These include high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS). HPLC is the most commonly used method for tetraglucoside analysis due to its high sensitivity and accuracy.

Biological Properties

Tetraglucoside has been shown to have prebiotic effects, promoting the growth of beneficial gut bacteria. It also exhibits antioxidant and anti-inflammatory properties, making it a potential therapeutic agent for various diseases. Furthermore, tetraglucoside has been shown to have immune-stimulating effects, which could make it a valuable ingredient in vaccines.

Toxicity and Safety in Scientific Experiments

Studies have shown that tetraglucoside is non-toxic and safe for human consumption at recommended doses. However, high doses of tetraglucoside may cause gastrointestinal discomfort and diarrhea.

Applications in Scientific Experiments

Tetraglucoside has potential applications in various scientific experiments, including microbiology, biochemistry, and biotechnology. It can be used as a growth medium for microbes and as a substrate for enzyme assays. In addition, tetraglucoside can be used in the food and cosmetic industries as a natural sweetener and moisturizer, respectively.

Current State of Research

Research on tetraglucoside is still ongoing, with many studies focusing on its potential therapeutic applications. Recent studies have shown that tetraglucoside has anti-cancer and anti-viral properties, and researchers are exploring its use in vaccine development and immunotherapy.

otential Implications in Various Fields of Research and Industry

Tetraglucoside has potential implications in various fields of research and industry, including the food, cosmetic, and pharmaceutical industries. It can be used as a natural sweetener in food products, a moisturizer in cosmetics, and a therapeutic agent in pharmaceuticals.

Limitations and Future Directions

Despite its many potential applications, tetraglucoside has some limitations, including its limited availability and high production costs. Future research should focus on developing more efficient and cost-effective methods for synthesizing tetraglucoside, as well as exploring new applications for this compound. Some possible future directions for research include:

1. Exploring the use of tetraglucoside in vaccine development and immunotherapy.

2. Investigating the potential of tetraglucoside as a food preservative.

3. Studying the effects of tetraglucoside on the gut microbiome and its implications for human health.

4. Developing new methods for producing high-purity tetraglucoside at a lower cost.

5. Investigating the potential of tetraglucoside as a treatment for inflammatory and autoimmune diseases.

6. Studying the impact of tetraglucoside on soil health and its potential use in sustainable agriculture.

7. Exploring the use of tetraglucoside in nanotechnology and other emerging technologies.

Conclusion

Tetraglucoside is a complex sugar with unique physical and chemical properties that make it a valuable compound for various industries. Its potential therapeutic applications, prebiotic effects, and antioxidant and anti-inflammatory properties make it an exciting area of research. Future research should focus on developing new applications for tetraglucoside and exploring its potential in emerging technologies.

CAS Number35175-16-7
Product NameTetraglucoside
IUPAC Name(2R,3R,4R,5R)-4-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-2,3,5,6-tetrahydroxyhexanal
Molecular FormulaC24H42O21
Molecular Weight666.6 g/mol
InChIInChI=1S/C24H42O21/c25-1-6(29)11(31)20(7(30)2-26)44-24-19(39)16(36)21(9(4-28)42-24)45-23-18(38)15(35)13(33)10(43-23)5-40-22-17(37)14(34)12(32)8(3-27)41-22/h1,6-24,26-39H,2-5H2/t6-,7+,8+,9+,10+,11+,12+,13+,14-,15-,16+,17+,18+,19+,20+,21+,22-,23+,24+/m0/s1
InChI KeyHDKHYSDETIRMHM-CDGFVBQXSA-N
SMILESC(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(OC(C(C3O)O)OC(C(CO)O)C(C(C=O)O)O)CO)O)O)O)O)O)O)O
Synonyms(Glc)4, Glc alpha 1-6 Glc alpha 1-4 Glc alpha 1-4 Glc, glucose tetrasaccharide
Canonical SMILESC(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(OC(C(C3O)O)OC(C(CO)O)C(C(C=O)O)O)CO)O)O)O)O)O)O)O
Isomeric SMILESC([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)CO)O)O)O)O)O)O)O


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