Sodium t-amyl oxide
Overview
Description
Sodium t-amyl oxide is a useful research compound. Its molecular formula is C10H22NaO and its molecular weight is 181.27 g/mol. The purity is usually 95%.
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Scientific Research Applications
Organic Synthesis
Sodium t-amyl oxide serves as a strong base in organic reactions, facilitating the deprotonation of weak acids. This property is essential for forming carbon-carbon bonds, which are crucial in synthesizing complex organic molecules. Its role in organic synthesis can be summarized as follows:
Polymer Chemistry
In polymer chemistry, this compound is utilized to synthesize polyolefins, which are essential for producing plastics and elastomers with enhanced properties. Its applications include:
| Application | Description |
|---|---|
| Polymerization | Facilitates the polymerization process to create high-performance materials. |
| Material Properties | Enhances the mechanical and thermal properties of polymers . |
Pharmaceutical Development
This compound plays a critical role in pharmaceutical development by acting as a reagent in the synthesis of drug intermediates. Its applications include:
Analytical Chemistry
In analytical chemistry, this compound enhances the sensitivity and selectivity of assays, making it valuable for quality control processes. Its contributions include:
| Application | Description |
|---|---|
| Assay Enhancement | Improves detection limits and specificity in chemical analyses. |
| Quality Control | Used in various assays to ensure compliance with regulatory standards . |
Environmental Applications
This compound has potential applications in environmental remediation, particularly in breaking down hazardous substances through chemical reactions. Its role includes:
| Application | Description |
|---|---|
| Contaminant Remediation | Utilized to degrade pollutants in contaminated sites through chemical reactions . |
Case Study 1: Organic Synthesis
A study demonstrated the use of this compound in synthesizing complex molecules such as alkaloids and terpenes through deprotonation reactions that facilitated carbon-carbon bond formation.
Case Study 2: Pharmaceutical Development
Research highlighted this compound's effectiveness in synthesizing pharmaceutical intermediates for anti-inflammatory drugs, showcasing its importance in drug discovery and development processes.
Case Study 3: Environmental Remediation
An investigation into the use of this compound for remediating soil contaminated with heavy metals showed promising results, indicating its potential for breaking down toxic substances effectively.
Properties
Molecular Formula |
C10H22NaO |
|---|---|
Molecular Weight |
181.27 g/mol |
InChI |
InChI=1S/C10H22O.Na/c1-7-9(3,4)11-10(5,6)8-2;/h7-8H2,1-6H3; |
InChI Key |
UIIJZQVROQHLAP-UHFFFAOYSA-N |
Canonical SMILES |
CCC(C)(C)OC(C)(C)CC.[Na] |
Origin of Product |
United States |
Synthesis routes and methods I
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Synthesis routes and methods II
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Please be aware that all articles and product information presented on BenchChem are intended solely for informational purposes. The products available for purchase on BenchChem are specifically designed for in-vitro studies, which are conducted outside of living organisms. In-vitro studies, derived from the Latin term "in glass," involve experiments performed in controlled laboratory settings using cells or tissues. It is important to note that these products are not categorized as medicines or drugs, and they have not received approval from the FDA for the prevention, treatment, or cure of any medical condition, ailment, or disease. We must emphasize that any form of bodily introduction of these products into humans or animals is strictly prohibited by law. It is essential to adhere to these guidelines to ensure compliance with legal and ethical standards in research and experimentation.
