14464-31-4
Chemical Structure
Palmitic acid N-hydroxysuccinimide
- CAS No.: 14464-31-4
- Formula:C20H35NO4
- Molecular Weight:353.50
IUPAC Name: 2,5-Dioxopyrrolidin-1-yl palmitate
InChIKey: OTNHQVHEZCBZQU-UHFFFAOYSA-N
SMILES: CCCCCCCCCCCCCCCC(ON1C(CCC1=O)=O)=O
Biological Activity: Palmitic acid N-hydroxysuccinimide is used to conjugate proteins to prepare targeted delivery vectors. Palmitic acid N-hydroxysuccinimide can be used as lipophilic electrophile. Palmitic acid N-hydroxysuccinimide can be used for the covalent connection between palmitic acid and ovalbumin. Palmitic acid N-hydroxysuccinimide can be used to synthesize cetacyl derivatives of amino acids, aminoacyl-trNA, coenzyme A, mercaptoacetic acid and other amino and thiogenic compounds[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Palmitic acid N-hydroxysuccinimide | 98.0% | Palmitic acid N-hydroxysuccinimide is used to conjugate proteins to prepare targeted delivery vectors. Palmitic acid N-hydroxysuccinimide can be used as lipophilic electrophile. Palmitic acid N-hydroxysuccinimide can be used for the covalent connection between palmitic acid and ovalbumin. Palmitic acid N-hydroxysuccinimide can be used to synthesize cetacyl derivatives of amino acids, aminoacyl-trNA, coenzyme A, mercaptoacetic acid and other amino and thiogenic compounds. | ||||||||||||||||||||
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References
- [1]. Al-Arif A, et al. Synthesis of fatty acyl CoA and other thiol esters using N-hydroxysuccinimide esters of fatty acids. J Lipid Res. 1969 May;10(3):344-5. [Content Brief]
- [2]. Haque Z, et al. Incorporation of fatty acid into food protein: palmitoyl soybean glycinin. Journal of Agricultural and Food Chemistry, 1982, 30(3): 481-486.
- [3]. Mowat AM, et al. Preparation of immune stimulating complexes (ISCOMs) as adjuvants. Curr Protoc Immunol. 2001 May;Chapter 2:Unit 2.11. [Content Brief]
