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Lauric acid N-hydroxy-succinimide ester manufacturers
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| | Lauric acid N-hydroxy-succinimide ester Basic information |
| Product Name: | Lauric acid N-hydroxy-succinimide ester | | Synonyms: | 2,5-Pyrrolidinedione, 1-[(1-oxododecyl)oxy]-;LAURIC ACID N-HYDROXYSUCCINIMIDE EST;SUCCINIMIDYL LAURATE;N-LAUROYLOXYSUCCINIMIDE;N-SUCCINIMIDYL DODECANOATE;Lauric acid-N-hydroxysuccinimide ester N-Succinimidyl dodecanoate;Lauric acid N-hydroxysuccinimide ester,Succinimidyl laurate;DODECANOIC ACID-N-HYDROXYSUCCINIMIDE ESTER | | CAS: | 14565-47-0 | | MF: | C16H27NO4 | | MW: | 297.39 | | EINECS: | | | Product Categories: | | | Mol File: | 14565-47-0.mol |  |
| | Lauric acid N-hydroxy-succinimide ester Chemical Properties |
| Melting point | 76-77 °C | | Boiling point | 392.3±25.0 °C(Predicted) | | density | 1.07±0.1 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | color | White to Off-White | | InChI | InChI=1S/C16H27NO4/c1-2-3-4-5-6-7-8-9-10-11-16(20)21-17-14(18)12-13-15(17)19/h2-13H2,1H3 | | InChIKey | LRKGVVJOUNKTGG-UHFFFAOYSA-N | | SMILES | C(ON1C(=O)CCC1=O)(=O)CCCCCCCCCCC |
| WGK Germany | 3 | | Storage Class | 13 - Non Combustible Solids |
| | Lauric acid N-hydroxy-succinimide ester Usage And Synthesis |
| Uses | (2,5-Dioxopyrrolidin-1-yl) dodecanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | | Biochem/physiol Actions | Lauric acid N-hydroxysuccinimide ester may be used for the synthesis of N-acylamino acids and lipidization of polypeptides or other applications that use N-hydroxysuccinimide ester conjugation chemistry. | | Synthesis | General procedure: lauric acid (12.0 g, 60 mmol) was dissolved in anhydrous ethyl acetate (100 mL), followed by slow addition of this solution to a solution of anhydrous ethyl acetate (300 mL) containing N-hydroxysuccinimide (NHS) (6.9 g, 60 mmol) and N,N'-dicyclohexylcarbodiimide (DCC) (12.4 g, 60 mmol). . The reaction mixture was stirred overnight at room temperature. After completion of the reaction, the by-product dicyclohexylurea (DCU) was removed by filtration. The filtrate was concentrated under reduced pressure to afford the white crystalline product 2,5-dioxopyrrolidin-1-yl dodecanoate (17.4 g, 95% yield). For further purification, the product was recrystallized with ethanol to give a final pure product of 16.6g. | | References | [1] Journal of the American Chemical Society, 2015, vol. 137, # 24, p. 7692 - 7705
[2] Journal of the American Chemical Society, 2003, vol. 125, # 40, p. 12110 - 12111
[3] RSC Advances, 2015, vol. 5, # 81, p. 66339 - 66354
[4] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 6, p. 1763 - 1767
[5] Synthetic Communications, 2009, vol. 39, # 24, p. 4467 - 4472 |
| | Lauric acid N-hydroxy-succinimide ester Preparation Products And Raw materials |
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