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  • 149342-80-3 , 正辛基-a-D-吡喃半乳糖苷,Octyl a-D-galactopyranoside
149342-80-3 , 正辛基-a-D-吡喃半乳糖苷,Octyl a-D-galactopyranoside

149342-80-3 , 正辛基-a-D-吡喃半乳糖苷,Octyl a-D-galactopyranoside

149342-80-3 ,正辛基-a-D-吡喃半乳糖苷 ,
Octyl a-D-galactopyranoside,
Cas:149342-80-3
C14H28O6 / 292.37
MFCD18642960

Octyl a-D-galactopyranoside

正辛基-a-D-吡喃半乳糖苷 ,

Octyl alpha-D-galactopyranoside (OAG) is a non-ionic detergent that has been widely used in biochemical and biophysical research for decades. This paper aims to provide a comprehensive overview of OAG, including 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:

Octyl alpha-D-galactopyranoside (OAG) is a sugar-based detergent that belongs to the alkyl glycoside class of non-ionic detergents. It is a white crystalline powder with a molecular weight of 292.4 g/mol. OAG was first synthesized in the 1970s and has been used to solubilize and study various membrane-associated proteins.

Physical and Chemical Properties:

OAG is sparingly soluble in water and forms micelles in aqueous solutions. It has a critical micelle concentration (CMC) of 2.17 mM at 25°C. The solubility of OAG depends on temperature and pH, and it has been found to be more soluble at high temperatures and low pH. OAG has a melting point of 129-131°C .

Synthesis and Characterization:

OAG can be synthesized by reacting octanol with alpha-galactose in the presence of an acid catalyst. The resulting product is then purified through recrystallization. OAG can be characterized by various methods, including nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, infrared (IR) spectroscopy, and X-ray crystallography.

Analytical Methods:

OAG can be analyzed using various analytical techniques, including high-performance liquid chromatography (HPLC) and gas chromatography (GC). HPLC is commonly used to determine the purity of OAG samples, while GC is used to determine the fatty acid composition of OAG.

Biological Properties:

OAG has been shown to have a wide range of biological properties, including membrane solubilization, membrane protein extraction, and enzyme stabilization. OAG has been used to study various membrane-associated proteins, including G protein-coupled receptors, ion channels, and transporters.

Toxicity and Safety in Scientific Experiments:

OAG is considered to be biocompatible and has been shown to be non-toxic at relatively high concentrations. However, the use of OAG should be carefully monitored, and appropriate safety measures should be taken to avoid exposure to eyes and skin.

Applications in Scientific Experiments:

OAG has been widely used in scientific experiments for various applications, including solubilization of membrane proteins, extraction of membrane-associated proteins, stabilization of enzymes, and as a non-ionic detergent in protein purification.

Current State of Research:

OAG has been extensively studied in the past few decades, and its properties and applications have been well-established. However, new research continues to explore the use of OAG in various fields of research, including biotechnology, pharmaceuticals, and materials science.

Potential Implications in Various Fields of Research and Industry:

OAG has a wide range of potential applications in various fields of research and industry, including drug discovery, biotechnology, and materials science. OAG can be used to study various membrane-associated proteins, which have significant implications for drug discovery and development. In addition, OAG can be used to stabilize and protect enzymes, which can be useful in various industrial applications.

Limitations and Future Directions:

Despite its widespread use, OAG has some limitations, including its low solubility in water and its potential to form aggregates at high concentrations. Future research should focus on developing new synthetic methods to improve the solubility and stability of OAG and exploring its applications in various fields, including drug delivery and diagnostics.

Future Directions:

1. Development of new synthetic methods to improve the solubility and stability of OAG.

2. Exploration of the use of OAG in drug delivery and diagnostics.

3. Investigation of the potential of OAG in materials science, including self-assembly and nanotechnology.

4. Study of the efficacy and safety of OAG in clinical applications.

5. Development of OAG-based detergents with improved performance and biocompatibility.

6. Exploration of the potential of OAG in environmental applications, such as wastewater treatment.

7. Investigation of the interactions between OAG and other biomolecules, including lipids and proteins.

8. Development of new analytical methods for the detection and quantification of OAG in biological and environmental samples.

9. Study of the effect of temperature and pH on the properties and applications of OAG.

10. Investigation of the potential of OAG in the formulation of new drugs and vaccines.

CAS Number149342-80-3
Product Nameoctyl alpha-D-galactopyranoside
IUPAC Name(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol
Molecular FormulaC14H28O6
Molecular Weight292.37 g/mol
InChIInChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11+,12+,13-,14+/m1/s1
InChI KeyHEGSGKPQLMEBJL-HTOAHKCRSA-N
SMILESCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
Canonical SMILESCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
Isomeric SMILESCCCCCCCCO[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O


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