13042-39-2 , Dianhydro-2-O-acetyl-D-glucitol,
二脱水-2-O-乙酰基-D-葡萄糖醇,
CAS:13042-39-2
C8H12O5 /188.18
MFCD09264290
二脱水-2-O-乙酰基-D-葡萄糖醇
1,4:3,6-Dianhydro-2-O-acetyl-D-glucitol is a direct and efficient biocatalyst for the production of lipase. It is a highly active immobilized enzyme that has been used to produce biodiesel. The immobilized 1,4:3,6-dianhydro-2-O-acetyl-D-glucitol can be recycled and reused as many times as desired with little loss of activity. This enzyme is also a biodegradable and degradable substrate that can be used in an oral dosage form for the treatment of obesity. 1,4:3,6-Dianhydro-2-O-acetyl-D-glucitol has been shown to have excellent stability at high substrate concentrations which makes it scalable and offers potential for large production volumes.
1,4:3,6-Dianhydro-D-glucitol 2-acetate, commonly known as isomaltulose, is a natural sugar substitute that has been gaining popularity in recent years due to its unique physical and chemical properties. This paper will provide an in-depth analysis of isomaltulose, covering topics such as its definition, 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.
Synthesis and Characterization:
Isomaltulose can be produced by enzymatic rearrangement of sucrose using isomerase. The resulting product is a mixture of isomaltulose and trehalulose, which can be separated using chromatography. The purity of isomaltulose can be determined using high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). Isomaltulose can also be characterized using nuclear magnetic resonance (NMR) and infrared (IR) spectroscopy.
Analytical Methods:
Isomaltulose can be quantified using HPLC, GC-MS, and polarimetry. HPLC is commonly used to determine the purity of isomaltulose, while GC-MS is used to identify and quantify isomaltulose in complex mixtures. Polarimetry is used to measure the optical rotation of isomaltulose, which is a function of its specific rotation. Isomaltulose can also be detected using thin-layer chromatography (TLC) and capillary electrophoresis (CE).
Biological Properties:
Isomaltulose is metabolized more slowly than sucrose because it requires hydrolysis by sucrase before it can be absorbed into the bloodstream. As a result, isomaltulose has a lower glycemic index (GI) than sucrose, which means it does not cause a rapid spike in blood glucose levels. Isomaltulose has been shown to have beneficial effects on insulin sensitivity, satiety, and fat oxidation. It is also less cariogenic than sucrose because it is not metabolized by cariogenic bacteria in the mouth.
Toxicity and Safety in Scientific Experiments:
Isomaltulose has been shown to be safe for human consumption at levels up to 50 grams per day. It has been approved as a food additive in the European Union, Japan, and the United States. Isomaltulose has also been shown to be non-toxic in animal studies, with no adverse effects observed at levels up to 10% of the diet.
Applications in Scientific Experiments:
Isomaltulose has a variety of applications in scientific experiments, including as a sweetener in food and beverages, as a source of energy in sports nutrition, and as a nutraceutical in functional foods. Isomaltulose is also being investigated for its potential applications in the treatment of obesity, diabetes, and other metabolic disorders.
Current State of Research:
There is growing interest in isomaltulose as a natural sugar substitute that provides a slow, sustained source of energy without causing a rapid spike in blood glucose levels. Isomaltulose has been shown to have beneficial effects on insulin sensitivity, satiety, and fat oxidation, making it a promising candidate for the prevention and treatment of metabolic disorders. Research is also ongoing to optimize the production of isomaltulose using novel enzymes and bioprocesses.
Potential Implications in Various Fields of Research and Industry:
Isomaltulose has potential implications in a variety of fields of research and industry. In the food and beverage industry, isomaltulose can be used as a low-glycemic sweetener that provides a slow, sustained source of energy. In the sports nutrition industry, isomaltulose can be used as a source of carbohydrate that provides sustained endurance. In the pharmaceutical industry, isomaltulose has potential applications in the treatment of obesity, diabetes, and other metabolic disorders.
Limitations and Future Directions:
Despite the promising potential of isomaltulose, there are some limitations and future directions that need to be addressed. For example, the production of isomaltulose is currently expensive and requires specialized enzymes and bioprocesses. In addition, more research is needed to determine the long-term safety and efficacy of isomaltulose in human subjects. Future directions for research could include the development of novel enzymes and bioprocesses for more efficient and cost-effective production of isomaltulose, as well as the development of new applications for isomaltulose in the treatment of metabolic disorders.
In conclusion, isomaltulose is a natural sugar substitute that has unique physical and chemical properties. It provides a slow, sustained source of energy and has a lower glycemic index than sucrose, making it a promising candidate for the prevention and treatment of metabolic disorders. However, more research is needed to optimize its production, determine its long-term safety and efficacy, and develop novel applications in various fields of research and industry.
CAS Number | 13042-39-2 |
Product Name | 1,4:3,6-Dianhydro-D-glucitol 2-acetate |
IUPAC Name | [(3R,3aR,6S,6aR)-3-hydroxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-6-yl] acetate |
Molecular Formula | C8H12O5 |
Molecular Weight | 188.18 g/mol |
InChI | InChI=1S/C8H12O5/c1-4(9)13-6-3-12-7-5(10)2-11-8(6)7/h5-8,10H,2-3H2,1H3/t5-,6+,7-,8-/m1/s1 |
InChI Key | ASUQMWUAFHPXOG-ULAWRXDQSA-N |
SMILES | CC(=O)OC1COC2C1OCC2O |
Canonical SMILES | CC(=O)OC1COC2C1OCC2O |
Isomeric SMILES | CC(=O)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2O |
CAS No: 13042-39-2 Synonyms: Isosorbide-2-acetate MDL No: MFCD09264290 Chemical Formula: C8H12O5 Molecular Weight: 188.18 |
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