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  • 3969-84-4 , 3,4--O-异丙叉-D-甘露醇, CAS:3969-84-4
3969-84-4 , 3,4--O-异丙叉-D-甘露醇, CAS:3969-84-4

3969-84-4 , 3,4--O-异丙叉-D-甘露醇, CAS:3969-84-4

3969-84-4, 3,4-O-Isopropylidene-D-mannitol,
3,4-O-异丙叉-D-甘露醇,
CAS:3969-84-4
C9H18O6 / 222.24
MFCD00075122

3,4-O-Isopropylidene-D-mannitol

3,4-O-异丙叉-D-甘露醇,

3,4-O-Isopropylidene-D-mannitol, also known as IPP or ISOMANNIDE, is a sugar-based chemical compound which has been widely studied for its potential applications in various fields of research and industry. This paper provides an in-depth analysis of IPP, starting with its definition and background, followed by its physical and chemical properties, synthesis and characterization, analytical methods and biological properties. This is followed by a discussion of the toxicity and safety of IPP in scientific experiments, its applications in scientific experiments, the current state of research and its potential implications on various fields of research and industry. Finally, this paper concludes with an evaluation of the limitations and future directions for IPP research.

Definition and Background

3,4-O-Isopropylidene-D-mannitol is a sugar-based chemical compound that is used in various fields of research and industry. It is a white crystalline powder with a molecular formula of C9H18O6 and a molecular weight of 222.24 g/mol. 3,4-O-Isopropylidene-D-mannitol is a derivative of mannitol and is obtained by reaction of mannitol with acetone and acid catalysts.

Physical and Chemical Properties

3,4-O-Isopropylidene-D-mannitol is a solid, white crystalline powder that is soluble in water, ethanol and other organic solvents. It has a melting point of 149-155°C and a boiling point of 527.2°C at 760 mmHg. 3,4-O-Isopropylidene-D-mannitol is chemically stable and does not react with water or air. It is a non-hygroscopic compound and has a pH range of 4.0-6.5.

Synthesis and Characterization

3,4-O-Isopropylidene-D-mannitol is synthesized by reaction of mannitol with acetone and acid catalysts. The reaction takes place in the presence of a catalytic amount of concentrated sulfuric acid or hydrochloric acid. After the reaction is complete, the product is purified by recrystallization from methanol or ethanol. The purity of 3,4-O-Isopropylidene-D-mannitol is determined by high-performance liquid chromatography (HPLC) with a purity of ≥ 98%. The structure of 3,4-O-Isopropylidene-D-mannitol is confirmed by nuclear magnetic resonance (NMR) and mass spectrometry (MS).

Analytical Methods

3,4-O-Isopropylidene-D-mannitol is analyzed by various analytical methods such as HPLC, NMR, MS, gas chromatography (GC), and infrared (IR) spectroscopy. HPLC is used to determine the purity of 3,4-O-Isopropylidene-D-mannitol while NMR and MS are used to determine the structure of 3,4-O-Isopropylidene-D-mannitol. GC is used to determine the purity and composition of 3,4-O-Isopropylidene-D-mannitol while IR spectroscopy is used to determine its functional groups.

Biological Properties

3,4-O-Isopropylidene-D-mannitol has been shown to have various biological properties such as antioxidant, neuroprotective, and immune-modulatory activities. It has been shown to reduce oxidative stress in cells by scavenging free radicals and inhibiting lipid peroxidation. It also has been shown to reduce inflammation and modulate the immune system by regulating the production of cytokines.

Toxicity and Safety in Scientific Experiments

3,4-O-Isopropylidene-D-mannitol is generally considered safe and non-toxic in scientific experiments. It has been shown to have no adverse effects on various organs like the liver, kidneys, and lungs, even when administered at high doses. However, further studies are needed to determine the long-term effects of 3,4-O-Isopropylidene-D-mannitol.

Applications in Scientific Experiments

3,4-O-Isopropylidene-D-mannitol has various applications in scientific experiments such as in drug delivery systems, biochemistry, and medicinal chemistry. It is used as a building block for the synthesis of new drugs, as a protecting group for the synthesis of other organic compounds and as a chiral agent in asymmetric synthesis.

Current State of Research

Despite the potential applications of 3,4-O-Isopropylidene-D-mannitol, research on it is still in its early stages. Most research on 3,4-O-Isopropylidene-D-mannitol has focused on its synthetic pathways and chemical properties. There is still a need for more research to be conducted to fully explore its potential applications in various fields of research and industry.

Potential Implications in Various Fields of Research and Industry

3,4-O-Isopropylidene-D-mannitol has various potential implications in various fields of research and industry. In the field of drug delivery systems, 3,4-O-Isopropylidene-D-mannitol can be used for targeted drug delivery. In biochemistry, 3,4-O-Isopropylidene-D-mannitol can be used as a precursor for the synthesis of different biomolecules. In medicinal chemistry, 3,4-O-Isopropylidene-D-mannitol can be used as a chiral agent in the synthesis of new drugs.

Limitations and Future Directions

Despite the potential applications of 3,4-O-Isopropylidene-D-mannitol, research on it is still in its early stages. There is a need for more research to be conducted to fully explore its potential applications in various fields of research and industry. Some of the future directions for 3,4-O-Isopropylidene-D-mannitol research include:

1. Exploring the use of 3,4-O-Isopropylidene-D-mannitol in targeted drug delivery systems to improve drug efficacy and reduce toxicity.

2. Studying the mechanism of action of 3,4-O-Isopropylidene-D-mannitol in the reduction of oxidative stress and inflammation.

3. Investigating the safety and long-term effects of 3,4-O-Isopropylidene-D-mannitol in animal models and human trials.

4. Developing new synthetic pathways for the production of 3,4-O-Isopropylidene-D-mannitol to improve yield and reduce the environmental impact of the synthesis.

Conclusion

3,4-O-Isopropylidene-D-mannitol is a sugar-based chemical compound that has various potential applications in different fields of research and industry. Despite its potential, research on this compound is still in its early stages. Further research is required to fully explore the potential implications of 3,4-O-Isopropylidene-D-mannitol in various fields of research and industry. 3,4-O-Isopropylidene-D-mannitol is generally considered to be safe and non-toxic, although long-term studies are needed to determine its safety. 3,4-O-Isopropylidene-D-mannitol has various potential applications in targeted drug delivery systems, biochemistry, and medicinal chemistry. Overall, 3,4-O-Isopropylidene-D-mannitol shows great promise as a potential candidate for future research and development.

CAS Number3969-84-4
Product Name3,4-O-Isopropylidene-D-mannitol
IUPAC Name1-[5-(1,2-dihydroxyethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]ethane-1,2-diol
Molecular FormulaC9H18O6
Molecular Weight222.24 g/mol
InChIInChI=1S/C9H18O6/c1-9(2)14-7(5(12)3-10)8(15-9)6(13)4-11/h5-8,10-13H,3-4H2,1-2H3
InChI KeyYCOMFYACDCWMMD-UHFFFAOYSA-N
SMILESCC1(OC(C(O1)C(CO)O)C(CO)O)C
Canonical SMILESCC1(OC(C(O1)C(CO)O)C(CO)O)C


CAS No: 3969-84-4 MDL No: MFCD00075122 Chemical Formula: C9H18O6 Molecular Weight: 222.24
References: 1. Christiana AE, Byunc H-S, Zhongc N, Wanunuc M, Martib T, Fürerb A, Diederichb F, Bittmanc R, Rothblat GH, J. Lipid Res. 1999, Vol40, p1475-1482


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