Nom du produit:1-Bromodocosane
IUPAC Name:1-bromodocosane
| Unité d'emballage | Stock disponible | Prix($) | Quantité |
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| CM361164-25g | in stock | NJƓ |
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| CM361164-100g | in stock | ůƓƓ |
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| Product Overview |
1-Bromodocosane is a long-chain aliphatic hydrocarbon compound. It is a branched alkane, meaning it has a single carbon-carbon bond that connects two different carbon atoms. It is a colorless liquid at room temperature and is highly flammable. It is a member of the aliphatic hydrocarbons family and is the most widely used branched alkane for laboratory experiments. |
| Synthesis Method |
1-Bromodocosane is typically synthesized through the process of halogenation. Halogenation is a reaction in which a halogen (e.g. chlorine, bromine, etc.) is added to an organic molecule to produce a halogenated compound. In the case of 1-Bromodocosane, the reaction involves the addition of bromine to a long-chain alkane, such as dodecane. The reaction is typically carried out in a solvent such as carbon tetrachloride (CCl4) at a temperature of 80-90°C. |
| Chemical Properties |
1-Bromodocosane is non-toxic, non-carcinogenic, and has a low reactivity. In addition, it is highly soluble in a variety of solvents and can be used as a solvent for a wide range of reactions. It is flammable and must be handled with care. In addition, it is not as reactive as other halogenated compounds, making it less suitable for certain applications. |
| Synthesis and Application |
1-Bromodocosane is a valuable compound for laboratory experiments due to its high solubility, low toxicity, and low reactivity. It can be used as a solvent for a variety of reactions, as a reactant in halogenation reactions, and as a lubricant in high-temperature applications. In addition, 1-Bromodocosane has been used in a range of scientific research applications, including studies of the structure and dynamics of biological membranes, the structure of proteins, and the structure of crystals. |
| Future Directions |
Future research could focus on developing new synthesis methods for the compound, as well as exploring its potential uses as a solvent, a reactant, and a lubricant. Additionally, further research into the biochemical and physiological effects of 1-Bromodocosane could be conducted to better understand its safety profile. Finally, further research into the mechanism of action of 1-Bromodocosane could be conducted to better understand its effects on biological systems. |
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