Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Dodecyldimethylamine oxide

Ci2H25NMe20" Dodecyldimethylamine oxide C12H25NMe2(CH2)3S03 12-3 Zwittergent, Sulfobetaine R0(CH2CH20) (CH2)20H Brij, Igepal, Triton 2 x 1(T3... [Pg.216]

Dodecyldimethylamine oxide [1643-20-5] M 229.4. Crystd from acetone or ethyl acetate. [Bunton et al. JOC 52 3832 7957]. [Pg.205]

Bakshi, M. S., R. Crisantino, R. De Lisi, and S. Milioto. 1993. Volume and heat capacity of sodium dodecyl sulfate-dodecyldimethylamine oxide mixed micellAsPhys. Cherr07 6914-6919. [Pg.299]

It appears that for each snrfactant system, AG° is a linear fnnction of the number of carbon atoms of the solubihzate see, for example, the work by DeLisi and co-workers who have stndied alcohol solubilization in SDS, dodecyltrimethylammonium bromide, and dodecyldimethylamine oxide.In this work we prefer to plot AG" as a fimction of the niunber of CH2 groups of the solubilizate. Tables 6.2 through 6.6 contain data for several homologous series in anionic, cationic, and nonionic surfactants, and on this basis the following relationship has been tested ... [Pg.374]

The table shows that, in dodecyldimethylamine oxide production, the use of USA storage grade H202 reduces nitrosamines by a factor of 3. Addition of a phosphonate based H202 stabilisation package reduces this level by a factor of 5 whilst increasing yield and conversion. [Pg.124]

Dodecyl dimethylamine N-Dodecyl dimethylamine. See Dimethyl lauramine Dodecyidimethylamine oxide N-Dodecyldimethylamine oxide. See Lauramine oxide... [Pg.1574]

Brackman, J. C. and J. B. F. N. Engberts (1992). Effect of surfactant charge on polymer-micelle interactions -Dodecyldimethylamine oxide. Langmuir 8(2) 424-428. [Pg.678]

Aliphatic tertiary amines can be oxidised to A-oxides using 35% w/w H2O2 alone [149], typically in water at 1.1 1.0 molar ratio for 4-5 hours at 60-65°C (example for dodecyldimethylamine). This reaction is employed worldwide on a scale in excess of 25 ktpa, to make fatty amine oxides, which are used as surfactants [150] in personal care products (e.g. shampoos) and as thickener components in hypochlorite household bleach. N-Methylmorpholine A-oxide has a growing use as a solvent for cellulose in the manufacture of a new cellulose fibre [151]. Substituted oxazolidine N-oxides are relatively new user-friendly biocides [152]. A further application involving an aliphatic tertiary amine oxide intermediate is glyphosate manufacture (section 9.5.1.7.6). [Pg.284]


See other pages where Dodecyldimethylamine oxide is mentioned: [Pg.228]    [Pg.117]    [Pg.216]    [Pg.135]    [Pg.376]    [Pg.1098]    [Pg.228]    [Pg.117]    [Pg.216]    [Pg.135]    [Pg.376]    [Pg.1098]    [Pg.211]    [Pg.348]    [Pg.203]   
See also in sourсe #XX -- [ Pg.83 ]




SEARCH



Dodecyldimethylamine

© 2024 chempedia.info