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  • 173725-28-5 ,壬基-2-乙酰氨基-2-脱氧-β-D-葡萄糖苷, CAS:173725-28-5
173725-28-5 ,壬基-2-乙酰氨基-2-脱氧-β-D-葡萄糖苷, CAS:173725-28-5

173725-28-5 ,壬基-2-乙酰氨基-2-脱氧-β-D-葡萄糖苷, CAS:173725-28-5

173725-28-5 ,Nonyl 2-acetamido-2-deoxy-b-D-glucopyranoside,
CAS:173725-28-5
C17H33NO6 / 347.45
MFCD08703872

Nonyl 2-acetamido-2-deoxy-b-D-glucopyranoside

壬基-2-乙酰氨基-2-脱氧-β-D-葡萄糖苷

Nonyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a new type of cycle control method that has been developed for the stabilization of dynamically coordinated systems. It is based on the observation that stable cycles can be generated by coordinating the system with an electrode. The power consumption of this control method is lower than that of other methods, which makes it suitable for applications requiring high efficiency and low power consumption. Nonyl 2-acetamido-2-deoxy-b-D-glucopyranoside provides a new approach to dynamic coordination control in complex networks, which is based on the observation that stable cycles can be generated by coordinating the system with an electrode. This approach has low power consumption and high efficiency, making it suitable for applications requiring high efficiency and low power consumption.

Definition and Background:

Nonyl 2-acetamido-2-deoxy-beta-D-glucopyranoside (NAG) is a type of sugar derivative that is widely used in biochemical research. This compound is a nonionic detergent that is used to solubilize and purify membrane proteins, as well as other hydrophobic molecules. NAG is a member of the family of glucopyranosides and is the most commonly used among its group. It is manufactured commercially as a white powder and has the chemical formula C17H33NO6. NAG is also known by other names such as Nonyl-beta-D-glucoside, Nonyl glucoside, and Nonylglucoside.

Physical and Chemical Properties:

NAG is produced through a reaction between glucose and nonyl alcohol, which results in a sugar and hydrophobic tail combination. The major physical characteristic of NAG is its surfactant nature. This property gives it the ability to lower surface tension and stabilize emulsions and foams. NAG is soluble in water and organic solvents such as ethanol, chloroform, and acetone.

Synthesis and Characterization:

The synthesis of NAG can be done in the laboratory by reacting glucose with nonyl alcohol under specific conditions. The reaction results in the activation of the glucose molecule, followed by the addition of nonyl alcohol resulting in the formation of NAG. Various spectroscopic methods such as Mass Spectroscopy, Nuclear Magnetic Resonance (NMR), and Fourier Transform Infrared (FTIR) spectroscopy are used to characterize the synthesized molecule and ensure the purity of the final product.

Analytical Methods:

Numerous analytical methods have been developed for NAG's quantification, including Thin Layer Chromatography (TLC), High Performance Liquid Chromatography (HPLC), UV-Vis Spectrophotometry, and Fluorescence Spectroscopy. TLC and HPLC are based on the separation of different compounds from a mixture, while UV-Vis and Fluorescence Spectroscopy allow the detection and quantification of specific molecules in a sample.

Biological Properties:

NAG's amphiphilic nature allows it to interact with hydrophobic molecules and solubilize them, making it an essential component in many biochemical experiments. NAG is known to have low toxicity and is deemed safe for cellular and organismal studies. It has been demonstrated that NAG does not harm microbial cells at concentrations up to 1% w/v, and its bactericidal activity does not exceed that of other detergents.

Toxicity and Safety in Scientific Experiments:

Toxicity and safety are critical factors in scientific experimentation. Since NAG is widely used in biological research, it is essential to ensure that it is safe for experimental purposes. Studies have shown that NAG has low toxicity and is safe to use in cell culture and animal studies up to concentrations of 0.1% w/v and 10 mg/kg, respectively. However, high doses can be hazardous, leading to tissue damage in some organs.

Applications in Scientific Experiments:

NAG is a widely used detergent in many scientific experiments due to its characteristics such as solubilization of proteins, extraction of lipids and oligosaccharides, and purification of membrane proteins. It also maintains the native state of the solubilized proteins, an essential criteria when studying their biological activity. NAG is also used in preparing cell-free extracts, protein concentrates, and reconstitution of membrane proteins.

Current State of Research:

NAG is extensively used in the field of biochemistry, where it has become a popular tool for the solubilization and purification of integral membrane proteins. The use of NAG in these studies has led to the discovery of new functions of membrane proteins and indicates the potential of NAG in this area of research. Additionally, it is being tested for the production of biofuels, surfactants in biodegradable detergent formulations, and delivery systems in the pharmaceutical industry.

Potential Implications in Various Fields of Research and Industry:

NAG has the potential to be used in several fields of research, including food technology, plant biology, and biotechnology. The ability to solubilize hydrophobic molecules makes it useful for extracting compounds from natural sources such as plant extracts, aqueous tissues and soil samples. Additionally, NAG is used in the food industry, where it is used as an emulsifier and stabilizer in foods. Its biodegradability and low toxicity make it an ideal ingredient in eco-friendly detergent formulations.

Limitations and Future Directions:

Although NAG is a well-establish detergent, it has limitations in its use for certain experiments such as those involving hydrophobic proteins or lipid membranes or generating detergent-resistant proteins; there are efforts to modify and synthesize novel compounds that offer higher specificity and better solubilization. Potential directions of NAG involve tailoring the hydrophobic component to optimize the detergent's performance and exploring its application in nanotechnology.

Conclusion:

Nonyl 2-acetamido-2-deoxy-beta-D-glucopyranoside is a widely used amphiphilic compound that is essential in biochemical research. It is characterized by its low toxicity, biodegradability, and surfactant nature, which makes it an ideal compound for solubilizing hydrophobic molecules. Given its numerous applications in different fields of research and its promising potential, NAG will continue to be an essential tool in various areas of research and industry. While it has limitations, its future research shows potential for further discoveries, contributing to new and safer technologies.

CAS Number173725-28-5
Product NameNonyl 2-acetamido-2-deoxy-beta-D-glucopyranoside
IUPAC NameN-[(2R,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-nonoxyoxan-3-yl]acetamide
Molecular FormulaC17H33NO6
Molecular Weight347.45 g/mol
InChIInChI=1S/C17H33NO6/c1-3-4-5-6-7-8-9-10-23-17-14(18-12(2)20)16(22)15(21)13(11-19)24-17/h13-17,19,21-22H,3-11H2,1-2H3,(H,18,20)/t13-,14-,15-,16-,17-/m1/s1
InChI KeyCTRCWYGGVOETGG-WRQOLXDDSA-N
SMILESCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)NC(=O)C
Canonical SMILESCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)NC(=O)C
Isomeric SMILESCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)NC(=O)C
CAS No: 173725-28-5 MDL No: MFCD08703872 Chemical Formula: C17H33NO6 Molecular Weight: 347.45


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