Skip to Content
Merck
CN

P1162

Palmitic acid N-hydroxysuccinimide ester

≥98% (TLC)

Synonym(s):

N-(Palmitoyloxy)succinimide, N-Succinimidyl palmitate, Palmitic acid N-succinimidyl ester

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C20H35NO4
CAS Number:
14464-31-4
Molecular Weight:
353.50
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24898166
MDL number:
MFCD00050402
Beilstein/REAXYS Number:
1547411

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Palmitic acid N-hydroxysuccinimide ester, ≥98% (TLC)

InChI

1S/C20H35NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(24)25-21-18(22)16-17-19(21)23/h2-17H2,1H3

SMILES string

CCCCCCCCCCCCCCCC(=O)ON1C(=O)CCC1=O

InChI key

OTNHQVHEZCBZQU-UHFFFAOYSA-N

assay

≥98% (TLC)

form

powder

lipid type

saturated FAs

storage temp.

−20°C

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Palmitic acid N-hydroxysuccinimide ester has been used to couple a protein for fabrication of targeted delivery vehicles. It has also been used in the covalent attachment of palmitic acid to ovalbumin.
Useful in the synthesis of hexadecanoyl derivatives of amino- and thio-compounds such as amino acids, aminoacyl-tRNA, coenzyme A, thioglycolic acid, etc.

Biochem/physiol Actions

Palmitic acid N-hydroxysuccinimide ester is used in the covalent linking of protein to palmitic acid.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000460746
0000460745
0000460745
0000460746
0000380850

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Preparation of immune stimulating complexes (ISCOMs) as adjuvants
Mowat AM and Reid G
Current Protocols in Immunology, 16(1), 2-11 (1995)
Adam Edelstein et al.
Shock (Augusta, Ga.), 36(5), 451-457 (2011-09-23)
Translocation of bacteria and other luminal factors from the intestine following surgical injury can be a major driver of critical illness. Bile acids have been shown to play a key role in the loss of intestinal epithelial barrier function during
Cell-specific siRNA delivery by peptides and antibodies
Test, 502, 91-122 (2012)
Cell-specific siRNA delivery by peptides and antibodies
Methods in Enzymology, 502, 91-122 (2012)
Ana Rute Neves et al.
Nanotechnology, 26(49), 495103-495103 (2015-11-18)
Nanotechnology can be an important tool to improve the permeability of some drugs for the blood-brain barrier. In this work we created a new system to enter the brain by functionalizing solid lipid nanoparticles with apolipoprotein E, aiming to enhance
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service