Hexaethylene Glycol Di-p-toluenesulfonate
≥93%
- Product Code: 84355
CAS:
42749-27-9
| Molecular Weight: | 590.7 g./mol | Molecular Formula: | C₂₆H₃₈O₁₁S₂ |
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| EC Number: | MDL Number: | MFCD00319275 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Hexaethylene glycol di-p-toluenesulfonate is widely used as a versatile reagent in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of polyethylene glycol (PEG) derivatives, which are essential in bioconjugation and drug delivery systems. The compound is also employed in the creation of crown ethers and other macrocyclic structures, which are valuable in host-guest chemistry and molecular recognition processes. Additionally, it is utilized in the development of surfactants and emulsifiers due to its ability to modify solubility and stability in various formulations. Its role in crosslinking reactions makes it useful in polymer chemistry for creating networks with specific mechanical and chemical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.200 | 10-20 days | $125.86 |
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| 1.000 | 10-20 days | $431.13 |
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Hexaethylene Glycol Di-p-toluenesulfonate
Hexaethylene glycol di-p-toluenesulfonate is widely used as a versatile reagent in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of polyethylene glycol (PEG) derivatives, which are essential in bioconjugation and drug delivery systems. The compound is also employed in the creation of crown ethers and other macrocyclic structures, which are valuable in host-guest chemistry and molecular recognition processes. Additionally, it is utilized in the development of surfactants and emulsifiers due to its ability to modify solubility and stability in various formulations. Its role in crosslinking reactions makes it useful in polymer chemistry for creating networks with specific mechanical and chemical properties.
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