1,12-Dodecanedicarboxylic acid

In some reactions the compounds unsubstituted at nitrogen proved to be typical oxaziridines. So the classification as oxaziridines was never a problem. They can be cleaved by hydrolysis to give carbonyl compounds and hydrox-ylamine and can easily be reduced by iodide in acid solution to form iodine, the carbonyl compound, and ammonia. N-Alkylation by t-butyl chloride leads to the known Ai-t-butyloxaziridine. By the action of ferrous salts the diamide of dodecanedicarboxylic acid is formed, in analogy to the formation of 31. 

The polyamide from tr( s,trflns-diaminodicyclohexyl methane and dodecanedicarboxylic acid gives soft, smooth, silklike cloth. The diamine is synthesized from aniline and formaldehyde the mixture of cis.cis,... 

Napier and Thorp [319] developed a nucleic acid detection system based on the catalytic oxidation of guanine residues by a Ru(bpy)3 + mediator. Monolayers were self-assembled by immersion of ITO in 5 mM 1,12-dodecanedicarboxylic acid in hexadecane for 36-48 h. The electrodes were thoroughly rinsed with hexane to remove any physically adsorbed molecules. 

The ability of ozone to destroy the double C=C bonds in organic compounds is the reason for its wide application in the preparation of bifunctional compounds. This is the principle that lies in the organization of the manufacture of dodecanedicarboxylic acid (1) and azelaic acid (2). The initial substrate for the preparation of (1) is cyclododecane which is obtained from the trimerization of butadiene and partial hydrogenation and (2) is prepared on the base of oleic acid ... 

Monomer(s) structure acids S-(p-carboxyphenoxy) valeric, 8-(p-carboxyphenoxy) ootanoic, 1,3-bis(p-carboxyphenoxy) propane, 1,6-bis(p-oarboxyphenoxy) hexane, 1,6-bis(o-carboxyphenoxy) hexane, adipic, azeiaic, dodecanedicarboxylic, dodecanedioic, fumaric, isophthaiic, p-carboxyphenoxy acetic, pimelic, sebacic, suberic, terephthalic other erucic acid dimer, ricinoleic acid maleate, ricinoleic acid succinate, 12-hydroxystearic acid succinate photopolymerizable monomers, e.g., methacrylated sebacic acid Goepferich, A Tessmar, J, Adv. Dmg Delivery Rev., 54,911-32, 2002 Jain, J P Chirkara, D Kumar, N, Expert Opin. Drug Deliv., 5, 8,889-907,2008. 

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