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  • 7306-64-1  ,2,3;5,6-二-O-异丙叉- L-古洛糖酸-1,4-内酯,CAS:7306-64-1
7306-64-1  ,2,3;5,6-二-O-异丙叉- L-古洛糖酸-1,4-内酯,CAS:7306-64-1

7306-64-1 ,2,3;5,6-二-O-异丙叉- L-古洛糖酸-1,4-内酯,CAS:7306-64-1

7306-64-1 ,2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone,
2,3;5,6-二-O-异丙叉- L-古洛糖酸-1,4-内酯,
CAS:7306-64-1
C12H18O6 / 258.27
MFCD01863379

2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone

2,3;5,6-二-O-异丙叉- L-古洛糖酸-1,4-内酯

2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone is a methylated form of L-gulono-1,4-lactone which is a monosaccharide. The methylation of this compound makes it more soluble in water and lipids. This product can be synthesized to any desired purity and can be modified to suit the needs of the customer. The oligosaccharides produced from 2,3:5,6-Di-O-isopropylidene L -gulono 1,4 lactone are polysaccharides composed of repeating units of monosaccharides that are linked together by glycosidic bonds. Polysaccharides are complex carbohydrates that can be either linear or branched and have many different functions in living organisms.

2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone (DIK) is a chemical compound with a cyclic structure that belongs to the class of keto sugars. It has a white crystalline appearance and is soluble in water and some organic solvents. DIK has been extensively studied due to its potential applications in various fields of research and industry. In this paper, we will provide a comprehensive overview of DIK, including 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.

Definition and Background:

DIK is a keto sugar that was first synthesized in 1956 by Karl Folkers and coworkers. It is also known as diketogulonic acid but is commonly referred to as DIK. DIK is an important precursor of vitamin C, which is a vital nutrient for the human body. Vitamin C, also known as ascorbic acid, is an antioxidant that plays a crucial role in various metabolic processes in the body, including collagen synthesis, wound healing, and immune system function.

Synthesis and Characterization:

DIK can be synthesized through various methods, including the reaction of L-gulono-1,4-lactone with acetone and sulfuric acid or hydrochloric acid. The synthesis of DIK can also be achieved through microbial fermentation using microorganisms such as Gluconobacter oxydans, Gluconacetobacter diazotrophicus, and Gluconobacter industrialis. Characterization of DIK can be done using various techniques, including nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FTIR).

Analytical Methods:

DIK can be analyzed using various methods, including HPLC, GC-MS, and NMR. These methods allow for the accurate determination of DIK concentration and purity.

Biological Properties:

DIK has been shown to have a range of biological activities, including antioxidant, anti-inflammatory, and anticancer properties. DIK also has the potential to stimulate collagen production and enhance wound healing.

Toxicity and Safety in Scientific Experiments:

DIK has been shown to have a low toxicity profile in scientific experiments. However, like all chemicals, it should be handled with care and proper safety precautions should be followed when handling and using DIK.

Applications in Scientific Experiments:

DIK has various applications in scientific experiments, including its use as a precursor for the synthesis of vitamin C, as well as its use in the development of new drugs and therapies for various diseases, including cancer and diabetes.

Current State of Research:

The current state of research on DIK is focused on exploring its potential applications in various fields, including drug development, agriculture, and cosmetic and food industries. Researchers are also studying the mechanism of action of DIK and its effects on human health.

Potential Implications in Various Fields of Research and Industry:

DIK has the potential to have significant implications in various fields of research and industry. Its use as a precursor for the synthesis of vitamin C has important implications for the agricultural industry and for the production of vitamin C supplements. Additionally, its potential anticancer and anti-inflammatory properties could lead to the development of new drugs and therapies for various diseases.

Limitations and Future Directions:

While DIK has significant potential in various fields, there are also limitations to its use. One limitation is the low yield of DIK synthesis, which can limit its use in large-scale applications. Future research on DIK should focus on developing more efficient methods for its synthesis, as well as studying its potential applications in new areas, such as the development of biomaterials and drug delivery systems.

Additional Potential Future Directions:

1. Investigating the potential use of DIK in the development of new antibiotics and antimicrobial agents.

2. Studying the effects of DIK on the gut microbiome and its potential use as a prebiotic.

3. Exploring the use of DIK in the development of nanomaterials and other advanced materials.

4. Investigating the potential use of DIK in the treatment of neurodegenerative diseases, such as Alzheimer's disease.

5. Studying the effects of DIK on the immune system and its potential use in the treatment of autoimmune diseases.

6. Developing new methods for the large-scale production of DIK to expand its potential applications in various industries.

CAS Number7306-64-1
Product Name2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone
IUPAC Name(3aS,6R,6aS)-6-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-6,6a-dihydro-3aH-furo[3,4-d][1,3]dioxol-4-one
Molecular FormulaC12H18O6
Molecular Weight258.27 g/mol
InChIInChI=1S/C12H18O6/c1-11(2)14-5-6(16-11)7-8-9(10(13)15-7)18-12(3,4)17-8/h6-9H,5H2,1-4H3/t6-,7+,8-,9-/m0/s1
InChI KeyOFZPAXSEAVOAKB-KZVJFYERSA-N
SMILESCC1(OCC(O1)C2C3C(C(=O)O2)OC(O3)(C)C)C
Synonyms2,3:5,6-Bis-O-(1-methylethylidene)-L-gulonic Acid γ-Lactone; 2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone;
Canonical SMILESCC1(OCC(O1)C2C3C(C(=O)O2)OC(O3)(C)C)C
Isomeric SMILESCC1(OC[C@H](O1)[C@@H]2[C@H]3[C@@H](C(=O)O2)OC(O3)(C)C)C
CAS No: 7306-64-1 Synonyms: L-Gulonolactone diacetonide MDL No: MFCD01863379 Chemical Formula: C12H18O6 Molecular Weight: 258.27

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