Aminooxy-PEG4-alcohol
Catalog Number: BT-259375
CAS Number: 106492-60-8
Molecular Formula: C8H19NO5
Molecular Weight: 209.24
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
Aminooxy-PEG4-alcohol is a chemical compound that has gained significant attention in scientific research due to its unique properties and potential applications. It is a derivative of polyethylene glycol (PEG) that contains an aminooxy functional group, which allows for conjugation with various biomolecules.
Properties
CAS Number
106492-60-8
Product Name
Aminooxy-PEG4-alcohol
IUPAC Name
2-[2-[2-(2-aminooxyethoxy)ethoxy]ethoxy]ethanol
Molecular Formula
C8H19NO5
Molecular Weight
209.24
InChI
InChI=1S/C8H19NO5/c9-14-8-7-13-6-5-12-4-3-11-2-1-10/h10H,1-9H2
InChI Key
CMZGGYJEHLUUIG-UHFFFAOYSA-N
SMILES
C(COCCOCCOCCON)O
Solubility
Soluble in DMSO
Synonyms
Aminooxy-PEG4-alcohol
Method of Synthesis or Extraction
Aminooxy-Aminooxy-PEG4-alcohol4-alcohol can be synthesized using various methods, including the reaction of Aminooxy-PEG4-alcohol with aminooxyacetic acid or aminooxyethyl carbamate. The efficiency and yield of each method depend on the reaction conditions, such as temperature, pH, and reaction time. The use of aminooxyacetic acid as a starting material has been reported to yield a higher purity product with a higher yield compared to aminooxyethyl carbamate. However, the latter method is more commonly used due to its simplicity and availability of the starting material.
Environmental and safety considerations should be taken into account during the synthesis process. The reaction should be carried out in a well-ventilated area, and appropriate personal protective equipment should be worn. The starting materials and by-products should be disposed of properly to prevent environmental contamination.
Environmental and safety considerations should be taken into account during the synthesis process. The reaction should be carried out in a well-ventilated area, and appropriate personal protective equipment should be worn. The starting materials and by-products should be disposed of properly to prevent environmental contamination.
Chemical Structure and Biological Activity
Aminooxy-Aminooxy-PEG4-alcohol4-alcohol has a molecular weight of 232.3 g/mol and a chemical formula of C8H19NO5. The aminooxy functional group (-NH-O-) allows for conjugation with various biomolecules, such as proteins, peptides, and nucleic acids. The Aminooxy-PEG4-alcohol4 linker provides water solubility and biocompatibility.
The biological activity of aminooxy-Aminooxy-PEG4-alcohol4-alcohol is mainly attributed to its ability to react with aldehydes and ketones, forming stable oxime bonds. This reaction has been utilized in various applications, such as protein labeling, drug delivery, and bioconjugation. Aminooxy-Aminooxy-PEG4-alcohol4-alcohol has also been reported to exhibit anti-inflammatory and anti-tumor activities.
The biological activity of aminooxy-Aminooxy-PEG4-alcohol4-alcohol is mainly attributed to its ability to react with aldehydes and ketones, forming stable oxime bonds. This reaction has been utilized in various applications, such as protein labeling, drug delivery, and bioconjugation. Aminooxy-Aminooxy-PEG4-alcohol4-alcohol has also been reported to exhibit anti-inflammatory and anti-tumor activities.
Biological Effects
Aminooxy-Aminooxy-PEG4-alcohol4-alcohol has been shown to affect cell function and signal transduction pathways. It can be used to selectively label proteins and peptides, allowing for the study of their localization and function in cells. Aminooxy-Aminooxy-PEG4-alcohol4-alcohol has also been used in drug development, where it can be conjugated with drugs to improve their pharmacokinetic properties and target specificity.
Potential therapeutic and toxic effects of aminooxy-Aminooxy-PEG4-alcohol4-alcohol should be considered in its applications. While it has shown promise in anti-inflammatory and anti-tumor activities, further studies are needed to determine its efficacy and safety in clinical settings.
Potential therapeutic and toxic effects of aminooxy-Aminooxy-PEG4-alcohol4-alcohol should be considered in its applications. While it has shown promise in anti-inflammatory and anti-tumor activities, further studies are needed to determine its efficacy and safety in clinical settings.
Applications
Aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has various applications in medical, environmental, and industrial research. In medical research, it has been used in drug development, where it can improve the pharmacokinetic properties and target specificity of drugs. It has also been used in clinical trials for cancer treatment and imaging.
In environmental research, aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has been used to study the effects of pollutants on ecosystems. It can be conjugated with biomolecules to monitor their uptake and distribution in organisms. Aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has also been used in pollution management, where it can be used to remove pollutants from water and soil.
In industrial research, aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has been used in manufacturing processes to improve product quality and efficiency. It can be used to modify the surface properties of materials, such as coatings and membranes. Health and safety considerations should be taken into account during its use in industrial settings.
In environmental research, aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has been used to study the effects of pollutants on ecosystems. It can be conjugated with biomolecules to monitor their uptake and distribution in organisms. Aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has also been used in pollution management, where it can be used to remove pollutants from water and soil.
In industrial research, aminooxy-Aminooxy-Aminooxy-PEG4-alcohol4-alcohol4-alcohol has been used in manufacturing processes to improve product quality and efficiency. It can be used to modify the surface properties of materials, such as coatings and membranes. Health and safety considerations should be taken into account during its use in industrial settings.
Future Perspectives and Challenges
Current limitations in the use and study of aminooxy-Aminooxy-PEG4-alcohol4-alcohol include its stability and reactivity with other functional groups. Possible solutions and improvements include the development of more stable derivatives and the optimization of reaction conditions. Future trends and prospects in the application of aminooxy-Aminooxy-PEG4-alcohol4-alcohol in scientific research include its use in targeted drug delivery, imaging, and biosensing.
In conclusion, aminooxy-Aminooxy-PEG4-alcohol4-alcohol is a versatile compound with various applications in scientific research. Its unique properties, such as its ability to conjugate with biomolecules and form stable oxime bonds, make it a valuable tool in drug development, environmental research, and industrial applications. Further studies are needed to fully understand its biological activity and potential therapeutic and toxic effects.
In conclusion, aminooxy-Aminooxy-PEG4-alcohol4-alcohol is a versatile compound with various applications in scientific research. Its unique properties, such as its ability to conjugate with biomolecules and form stable oxime bonds, make it a valuable tool in drug development, environmental research, and industrial applications. Further studies are needed to fully understand its biological activity and potential therapeutic and toxic effects.
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