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Dimethylamino propylamine

Fig. 3.3 X-ray crystal structure of Im-HpPyPy-/ -Dp (Dp = dimethylamino-propylamine) bound in a 2 1 complex with its target DNA site, 5 -AGTACT-3 ... Fig. 3.3 X-ray crystal structure of Im-HpPyPy-/ -Dp (Dp = dimethylamino-propylamine) bound in a 2 1 complex with its target DNA site, 5 -AGTACT-3 ...
McFadden JP, Ross JS, White IR, Basketter DA. Clinical allergy to cocamidopropyl betaine reactivity to cocamido-propylamine and lack of reactivity to 3-dimethylamino-propylamine. Contact Dermatitis 2001 45(2) 72-4. [Pg.879]

Their synthesis begins with 3-(dimethylamino)propylamine (19), which is reacted in an inert solvent in the presence of a hydrocloride binding substance with chloroformic acid propyl ester (20) and chloroformic acid thiol ester (21), respectively. [Pg.454]

Heating (2-bromomethylphenyl)chloromethyldimethylgermane with the primary amines methyl-amine, 3-(dimethylamino)propylamine, or aniline affords the corresponding 3-substituted heterocyclic 3,1-benzazagermines (51) in high yields <88JOM(339)259>. [Pg.1143]

DIMETHYLAMINOPROPYLAMINE or 3-(DIMETHYLAMINO)PROPYLAMINE (109-55-7) Forms explosive mixture with air (flash point 100°F/38°C). Reacts violently with strong oxidizers, strong acids, cellulose nitrate, ethylene dichloride. Incompatible with organic anhydrides, isocyanates, aldehydes. [Pg.443]

Beilstein Handbook Reference) AI3-25441 1-Amino-3-dimethylaminopropane BRN 0605293 CCRIS 4799 EINECS 203-680-9 HSDB 5391 1-(Dimefhylamino)-3-aminopropane 3-(Dimethylamino)-propylamine y-(Dimethylamino)propylamine N,N-Di-methyl-1,3-diaminopropane NSC 1067 1,3-Propane-diamine, N,N-dimethyl- Propylamine, 3-(N,N-dimethyl-amino)-. [Pg.228]

CSI is reacted with a diamine (Dimethylamino propylamine), and Vistalon 4608 (EPDM rubber)... [Pg.320]

Synonyms MN-dimethyl-i,3-propanediamine N,N-dimethyl-i,3-diaminopropane 3-(dimethylamino)-propylamine dimethylamino-propylamine i-amino-3-dimethylaminopropane N,JV-dimethyl-N-(3-aminopropyl)amine 3-(dimethylamine)propylamine N,N-dimethyl-i,3-propylenediamine 3-(N,N-dimethylamino)propylamine 3-aminopropyldimethylamine DMPA Uses intermediate substance in the synthesis of alkylamidopropyldimethylamines/alkylamidobetaines found as an impurity in cosmetic surfactants present in e.g. shampoos hardener of epoxy resins additive in fuel, dyes, pesticides and binding agents in the production of ion-exchangers A... [Pg.1209]

Phthalocyanines may be regarded as benzopyrrole derivatives, and heating with excess chlorosulfonic acid at 125-130 °C converts them into sulfonyl chlorides. Heating copper phthalocyanine 67 with a mixture of thionyl chloride and chlorosulfonic acid followed by condensation of the resultant product with 3-methoxypropylamine and di(o-methylphenylamino)imine afforded a blue dye used for blue inks in ballpoint pens. Copper phthalocyanine 67, with chlorosulfonic acid and 3-(dimethylamino)propylamine, gave a precipitate which, on dissolution in an aqueous mixture of ethylene glycol-urea and treatment with aluminium sulfate, dyed paper a clear turquoise blue. Crude alpha-type... [Pg.194]

See other pages where Dimethylamino propylamine is mentioned: [Pg.130]    [Pg.299]    [Pg.437]    [Pg.461]    [Pg.463]    [Pg.525]    [Pg.48]    [Pg.178]    [Pg.315]    [Pg.395]    [Pg.693]    [Pg.727]    [Pg.332]    [Pg.965]    [Pg.1209]    [Pg.61]    [Pg.146]    [Pg.174]   
See also in sourсe #XX -- [ Pg.314 , Pg.315 ]



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