Dioctadecylamine
Dioctadecylamine structure
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Common Name | Dioctadecylamine | ||
|---|---|---|---|---|
| CAS Number | 112-99-2 | Molecular Weight | 521.98700 | |
| Density | 0.826g/cm3 | Boiling Point | 582.8ºC at 760mmHg | |
| Molecular Formula | C36H75N | Melting Point | 71-73ºC | |
| MSDS | USA | Flash Point | 197.2ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Self-assembly mechanism of nanoparticles of Ni-based Prussian Blue analogues at the air/liquid interface: a synchrotron X-ray reflectivity study.
ChemPhysChem 16 , 2549-55, (2015) Prussian Blue analogue (PBA) nanoparticles can be self-assembled at air/liquid interfaces to build novel materials with interesting magnetic features. Herein, we study the influence of the size of PBA Cs0.4 Ni[Cr(CN)6 ]0.9 and K0.25 Ni[Fe(CN)6 ]0.75 nanoparti... |
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Improving ready biodegradability testing of fatty amine derivatives.
Chemosphere 73(4) , 506-10, (2008) This study assesses the biodegradation potential of a number of fatty amine derivatives in tests following the OECD guidelines for ready biodegradability. A number of methods are used to reduce toxicity and improve the bioavailability of the fatty amine deriv... |
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Effect of the alkyl chain length of secondary amines on the phase transfer of gold nanoparticles from water to toluene.
Langmuir 30(23) , 6684-93, (2014) In the present paper we describe a phase transfer of aqueous synthesized gold nanoparticles (AuNPs) from water to toluene using secondary amines: dioctylamine, didodecylamine, and dioctadecylamine. The effect of the hydrocarbon chain length and amount of amin... |
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Study of molecular interactions between a phospholipidic layer and a pH-sensitive polymer using the Langmuir balance technique.
Langmuir 20(4) , 1393-400, (2004) Molecular interactions between a terminally alkylated pH-sensitive N-isopropylacrylamide copolymer DODA-poly(NIPAM-co-MAA) and a monolayer of distearoylphosphatidylcholine (DSPC) at the air/water interface are investigated using the Langmuir balance technique... |
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Galactose-containing amphiphiles prepared with a lipophilic radical initiator: association processes between liposomes triggered by enzymatic reaction.
Bioconjug. Chem. 6(4) , 361-6, (1995) A galactose-containing monomer (2-(methacryloyloxy)ethyl beta-D-galactopyranoside, MEGal) was polymerized by using a lipophilic radical initiator. The amphiphile obtained formed a liposome by mixing with bis(trans,trans-2,4-dioctadecadienoyl)phosphatidylcholi... |
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Biomimetic lipoglycopolymer membranes: photochemical surface attachment of supramolecular architectures with defined orientation.
Angew. Chem. Int. Ed. Engl. 48(37) , 6896-9, (2009)
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Molecular organization of histidine-tagged biomolecules at self-assembled lipid interfaces using a novel class of chelator lipids.
Proc. Natl. Acad. Sci. U. S. A. 92(20) , 9014-8, (1995) In molecular biology, the expression of fusion proteins is a very useful and well-established technique for the identification and one-step purification of gene products. Even a short fused sequence of five or six histidines enables proteins to bind to an imm... |
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PH-sensitive Dioctadecylamine-501 polymeric micelles for delivery of insulin.
J. Nanosci. Nanotechnol. 11(3) , 1823-33, (2011) In this work, fluorescently labeled smart micelle copolymers which consist of Dioctadecylamine-501 (DODA-501) as the hydrophobic segment, N-isopropylacrylamide (NIPAAm) as well as acrylic acid (AAc) as the hydrophilic segments were prepared. These micelles sh... |
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Liposome functionalization with copper-free "click chemistry".
J. Control. Release 202 , 14-20, (2015) The modification of liposomal surfaces is of interest for many different applications and a variety of chemistries are available that makes this possible. A major disadvantage of commonly used coupling chemistries (e.g. maleimide-thiol coupling) is the limite... |
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Synthesis of bisethylnorspermine lipid prodrug as gene delivery vector targeting polyamine metabolism in breast cancer.
Mol. Pharm. 9(6) , 1654-64, (2012) Progress in the development of nonviral gene delivery vectors continues to be hampered by low transfection activity and toxicity. Here we proposed to develop a lipid prodrug based on a polyamine analogue bisethylnorspermine (BSP) that can function dually as g... |