N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride
98.5%
- Product Code: 56663
Alias:
Related CAS: 7084-11-9; 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride; 1-ethyl-(3-dimethylaminopropyl) carbonyl di Imine hydrochloride; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; EDC hydrochloride
CAS:
25952-53-8
| Molecular Weight: | 191.7 g./mol | Molecular Formula: | C₈H₁₈ClN₃ |
|---|---|---|---|
| EC Number: | 247-361-2 | MDL Number: | MFCD00012503 |
| Melting Point: | 110-115 °C(lit.) | Boiling Point: | |
| Density: | 0.877 g/mL at 20 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used as a coupling agent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It is particularly effective in activating carboxylic acids, making them more reactive toward amines. In bioconjugation, it is employed to link biomolecules, such as proteins or nucleic acids, to other molecules or surfaces, which is essential in diagnostic assays and drug delivery systems. Additionally, it plays a role in the modification of polymers and the preparation of hydrogels, contributing to advancements in materials science and tissue engineering. Its applications also extend to organic synthesis, where it is used to create esters, thioesters, and other derivatives, enhancing the efficiency of chemical reactions.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 107 118? |
| PURITYAT | 98.5-101.5 |
| WATER BY KARL FISHER | 0-1 |
| APPEARANCE | WHITE POWDER OR CRYSTALS |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | €11.61 |
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| 25.000 | 10-20 days | €16.36 |
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| 100.000 | 10-20 days | €43.79 |
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| 500.000 | 10-20 days | €176.23 |
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| 2500.000 | 10-20 days | €779.85 |
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N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride
This chemical is widely used as a coupling agent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It is particularly effective in activating carboxylic acids, making them more reactive toward amines. In bioconjugation, it is employed to link biomolecules, such as proteins or nucleic acids, to other molecules or surfaces, which is essential in diagnostic assays and drug delivery systems. Additionally, it plays a role in the modification of polymers and the preparation of hydrogels, contributing to advancements in materials science and tissue engineering. Its applications also extend to organic synthesis, where it is used to create esters, thioesters, and other derivatives, enhancing the efficiency of chemical reactions.
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