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Results for “Dimethylamines”

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At least 163 records · Page 9Linked to original sources
PubMed1980

Liver and kidney tumors induced by N-nitroso-dimethylamine in Xenopus borealis (Parker).

N-nitroso-dimethylanine dissolved in aquarium water at a concentration of 400 ppm (1/4 of the LD50/30d) induced malignant tumors in 39 (54.2%) out of 72 young adult animals of the amphibian species Xenopus borealis. The first tumor was detected at 11 weeks, and the average latency was 35.1 weeks. Tumors were located in the liver (32 cholangiocarcinomas and 13 hepatocellular cancers) and the kidney (9 adenocarcinomas and 2 anaplastic cancers). Thirteen animals bore two or more types of tumors. These results demonstrate that a high percentage of tumors can be induced in amphibians by chemical carcinogens if appropriate methods are used.

Adenocarcinoma↗
PubMed1975

Carcinogenic N-nitro-dimethylamine from the reaction of the analgesic amidopyrine and nitrite extracted from foodstuffs.

The reaction of the analgesic amidopyrine (100 mg) with nitrite extracted from cured meats and from spinach in varying degrees of spoilage was studied. Unde physiological conditions the carcinogenic dimethylnitrosamine was formed at milligram levels at nitrite concentrations as low as 4 mg (in 175 ml extracted from 100 g boiled ham). The rate of decrease in concentration in the human stomach after ingestion of amidopyrine and of nitrite contained in boiled ham or in a broth from boiled ham was also measured.

Aminopyrine↗
PubMed2000

Effects of protonation on the thermodynamic properties of alkyl dimethylamine oxides.

The effects of protonation on alkyldimethyl amine oxide micelles are reviewed, mainly with regard to dodecyl and tetradecyl homologs. The topics discussed are hydrogen ion titration properties, critical micelle concentration (CMC), area per surfactant and micelle aggregation number. A hydrogen bond hypothesis is proposed to interpret the several characteristic results associated with protonation: between two cationic species as well as between the non-ionic-cationic pair. The dipole-dipole interaction of the non-ionic micelle is discussed in relation to both: (a) the unusually high CMC values of the non-ionic micelles compared with other non-ionic surfactants with the same hydrocarbon chain; and (b) the reversal of the stability of the non-ionic and the cationic micelles at high ionic strengths. Two different approaches of the salting out effect on the ionic micelles are compared, the Chan-Mukerjee approach and ours, in relation to the non-linear Corrin-Harkins relation. The obtained salting out constants of the surfactants carrying a dodecyl chain decreased as the head group becomes more polar. Infrared and 13C-NMR spectra data are examined from the point of the specific interaction claimed by the hydrogen bond model. Mixed surfactant systems including amine oxides and the solid state phase behavior of amine oxides are both briefly reviewed.

Journal Article↗
PubMed2005

Cleavage of hydrazine and 1,1-dimethylhydrazine by dinuclear tantalum hydrides: formation of imides, nitrides, and N,N-dimethylamine.

The complexes (RPh[NPN]Ta)2(mu-H)4 (RPh[NPN] = RP(CH2SiMe2NPh)2) activate molecular nitrogen to give (RPh[NPN]Ta)2(mu-eta1-eta2-N2)(mu-H)2; however, addition of hydrazine to (CyPh[NPN]Ta)2(mu-H)4 promotes cleavage of the N-N bond and N-H activation to give the bridging bisimide complex (CyPh[NPN]Ta)2(mu-H)2(mu-NH)2. Substitution of the phosphine substituent from cyclohexyl to phenyl allows for characterization of (PhPh[NPN]Ta)2(mu-H)2(mu-NH)2 crystallographically. Addition of the substituted hydrazine Me2NNH2 results in formation of a mono(nitride) complex, (RPh[NPN]Ta)2(mu-H)3(mu-N). The N-N bond has again been cleaved, but the second nitrogen atom has been functionalized and ejected as Me2NH.

Journal Article↗