L3900
Lauric acid N-hydroxysuccinimide ester
≥98% (TLC)
Synonym(s):
Succinimidyl laurate
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About This Item
Empirical Formula (Hill Notation):
C16H27NO4
CAS Number:
Molecular Weight:
297.39
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25
Recommended Products
assay
≥98% (TLC)
lipid type
saturated FAs
storage temp.
−20°C
SMILES string
CCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
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
InChI key
LRKGVVJOUNKTGG-UHFFFAOYSA-N
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.
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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A novel method allowing the conjugation of a fatty acid to a peptide or protein in aqueous buffer is described in this paper. L-Cysteinyl 2-pyridyl disulfide (CPD) (III), which was obtained by reacting L-cysteine (I) with 2,2-dithiopyridine (II), was reacted
Y Lapidot et al.
Journal of lipid research, 8(2), 142-145 (1967-03-01)
Several crystalline N-hydroxysuccinimide esters of short- and long-chain fatty acids have been synthesized. These compounds react with free amino acids to form preferentially N-acylamino acids. The reaction of the N-hydroxysuccinimide esters with hydroxylamine and the behavior of the N-acylamino acids
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