22543-30-2

Usage

Chemical Properties

White Solid

InChI:InChI=1/C12H25NO2.ClH/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15;/h1-11,13H2,(H,14,15);1H

Upstream product

• 693-57-2 12-Aminododecanoic acid 
• 947-04-6 2-azacyclotridecanone 
• 22915-49-7 11-cyanoundecanoic acid methyl ester 
• 14811-73-5 10-oxo-decanoic acid methyl ester 
• 111-81-9 Methyl 10-undecenoate 
• 112-38-9 10-undecenoic acid 
• 1395034-04-4 methyl 12-aminododecanoate acetic acid salt 

Downstream Products

• 4272-07-5 12-(((benzyloxy)carbonyl)amino)dodecanoic acid 
• 4271-88-9 Benzyloxycarbonyl-bis-(12-amino-dodecansaeure)-hydrazid 
• 4271-87-8 Benzyloxycarbonyl-bis-(12-amino-dodecansaeure)-methylester 

Relevant academic research and scientific papers

Divergent process for C10, C11 and C12 ω-amino acid and α,ω-dicarboxylic acid monomers of polyamides from castor oil as a renewable resource

Polyamides have great potentials for diverse applications and the present production of their monomers mostly relies on resources from fossil fuel. Starting from undecylenic acid, a natural resource, we have developed both divergent and efficient processes for C10, C11 and C 12 ω-amino acid and α,ω-dicarboxylic acid monomers of the polyamides.

Biologically compatible, phosphorescent dimetallic rhenium complexes linked through functionalized alkyl chains: Syntheses, spectroscopic properties, and applications in imaging microscopy

A range of luminescent, dimetallic complexes based upon the rhenium fac-tricarbonyl diimine core, linked by aliphatic chains of varying lengths and functionality, have been synthesized and their photophysical properties examined. Each complex displays characteristic 3MReL diimineCT emission in aerated acetonitrile solution, with long lifetimes in the range of 129-248 ns and corresponding quantum yields in the range 3.2-8.0%. In aqueous solution, as opposed to acetonitrile, the complexes generally show a small hypsochromic shift in λem and an extension of the 3MLCT lifetime, attributed to a hydrophobically driven association of the alkyl chains with the rhenium-bound diimine units. In live cell imaging experiments using MCF7 cells the complexes all show good uptake by non-energy dependent mechanisms without endosomal entrainment, and with varying propensity to localize in organelles. The degrees of uptake and localization properties are discussed in terms of the length and chemical nature of the linkers, and in terms of the likely interactions between these and the various cellular components encountered.

Transkarbams as transdermal permeation enhancers: Effects of ester position and ammonium carbamate formation

Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated with the carbamic acid salt and/or its decomposition in the acidic stratum corneum. The ammonium ester thereby released is an active enhancer species as well, and its activity highly depends on the position of the ester group.