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Phenylene di-amines

Fig. 3. Plot of the rate constant kg vs. AI for the electron transfer of Eq. (6). The scavengers used are named in the figure. Abbreviations mean BP — benzophenone, NA — naphthaline, TEA — triethylamine, TMPD — dimethyl-p-phenylene-di-amine. [From Ref 11, with permission of the editors.]... Fig. 3. Plot of the rate constant kg vs. AI for the electron transfer of Eq. (6). The scavengers used are named in the figure. Abbreviations mean BP — benzophenone, NA — naphthaline, TEA — triethylamine, TMPD — dimethyl-p-phenylene-di-amine. [From Ref 11, with permission of the editors.]...
The important tri-amino azo compound is the one in which two amino groups are in one ring, ortho and para to the azo group and one amino group meta to the azo group in the other ring. The constitution of the compound is proven by its preparation from meta-phenylene di-amine, we/a-di-amino benzene. This is diazotized so that only one... [Pg.574]

Thiourea derivatives 164 were prepared by Kaupp et al. by mechanochemical reactions in which stoichiometric quantities of solid o-phenylene-di-isothiocyanate 161 reacts with the solid aromatic amines 162 in a ball-mill at room tanperature (Retsch MM2(X)0 miU with a lOmL stainless steel beaker and balls) [31]. The products, l-(aminoaryl-thiocarbonyl)-benzimidazolidine-2-thiones 163 were presumably... [Pg.176]

Among the diamines suitable for the manuf of such explosives may be mentioned phenyl-ene-di(methyl amine) and phenylene-ditoluidine As an example of an explosive prepd from these diamines, Oliver (Ref 2) cites trinitro-p henylene-difmethylnitramine)... [Pg.131]

TCNE = Tetracyanoethylene Dipdba = 4,4 -diisopropyl(di-benzylideneacetone) TMM = Trimethylenemethane dppm = (Diphenylphosphino)methane MMLCT = Metal-metal bond to ligand charge-transfer Tp = Hydrido(trispy-razolyl)borate Tp = Hydridotris(3,5-dimethyl-pyrazolyl)bo-rate BAr = (3,5-triflnoromethylphenyl)borate ttab = l,2,4,5-tetrakis(l-iV-7-azaindolyl)benzene tmeda = Tetra-methylethylenediamine bpma = Bis(pyridyhnethyl)amine TFE = Triflnoroethanol dtbpm = Bis(di-terr-butylphosphi-no)methane dmpe = Bis(dimethylphosphino)ethane dcpe = Bis(dicyclohexylphosphino)ethane triphos = Bis(2-diphe-nylphosphinoethyl)phenylphosphine COD = 1,5-cycloocta-diene dppbts = (Diphenylphosphinobutane)tosylate sodium PPE = Poly(jo-phenylene ethylene). [Pg.3899]

Di(ethylamino)-benzene, l,2 Bis(ethyU amino)-benzene or o-Phenylene-bis(ethyl-amine), C(5H4(HN,C2H5)2, may be considered as the parent compd of its bis(trinitro) detiv, although not used to prep it... [Pg.119]

Additions of amine stabilizers greatly increase thermal stability of PA at long ageing [72]. For example, such antioxidants as - di - (3 - naphthyl - p - phenylene diamine ... [Pg.10]

Beilstein Handbook Reference) Aceto DIPP Agerite White AgeRite W AI3-14324 Antigene F Antioxidant 123 Antioxidant DNP ASM-DNT 1,4-Benzenediamine, N,N -di-2-naphthalenyl- N,N -Bis-(2-naftyl)-p-fenylendiamin 1,4-Bis(2-naphthylamino)-benzene N,N -Bis((3-naphthyl)-p-phenylenediamine N,N -Bis(2-naphthyl)-p-phenylenediamine BRN 2224419 CCRIS 6026 Oi-(3-naphthyl-p-phenyldi-amine Di-(J-naphthyl-p-phenylenediamine s-Di(P-naphthyl)-p-phenylenediamine N,N -Di-p-naphlhyl-p-phenylene-diamine N,N -Di-2-naphthalenyl-1,4-benz-enediamine N,N -Di-2-naphthyl-p-phenylenediamine Diafen NN DNPD Dnpda Dwu-p-naftylo-p-fenylodwuamina EINECS 202-249-2 Nonox CL NSC 3410 p-Phenylenediamine, N,N -(di-2-naphthyl)- N,N -p-Phenylenebis(2-naphthylamine) Santowhite CL Tisperse MB-2X. Antioxidant, An antidegradant for latex, nitrile rubber, styrene-butadiene and nitrile-butadiene rubber. Solid mp = 224-230° d n 1.22-1.28 insoluble in H2O, EtOH, soluble in organic solvents LDso (rat orl) = 4500 mg/kg. Vanderbilt R. T. Co. Inc. [Pg.14]

Naphthyl-p-phenylene diamine. See N,N -Di- 3-naphthyl-p-phenylenedi-amine... [Pg.1215]

Stabilizers UVA 2-hydroxy-4-octyloxybenzophenone 2-(2H-benzo-triazol-2-yl)-6-dodecyl-4-methylphenol, branched linear propanedioic acid, [(4-methoxyphenyl)-methylene]-dimethyl ester HAS 1,3,5-triazine-2,4,6-triamine, N,N [1,2-ethane-diyl-bis[[[4,6-bis[butyl(1,2,6,6-pentamethyl-4-piperidinyl) amino]-1,3,5-triazine-2-yl]imino]-3,1 -propanediyl]bis[N, N -dibutyl-N ,N -bis(1,2,2,6,6-pentamethyl-4-piperidinyl)- poly[[(6-[1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2,4-diyl] [2,2,6,6-tetramethyl-4-piperidinyl)imino]-1,6-hexanediyl[2,2,6,6-tetramethyl-4-piperidinyl)imino]] 1,6-hexanediamine- N,N -bis(2,2,6,6-tetramethyl-4-piperidinyl)-polymer with 2,4,6-trichlo-ro-1,3,5-triazine, reaction products with N-butyl-1-butanamine an N-butyl-2,2,6,6-tetramethyl-4-piperidinamine butanedioic acid, dimethylester, polymer with 4-hydroxy-2,2,6,6-tetrameth-yl-1-piperidine ethanol Phenolic antioxidant pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) Amine benzenamine, N-phenyl-, reaction products with 2,4,4-trimethylpentene Optical brightener 2,2 -(1,2-ethyl-enediyldi-4,1-phenylene)bisbenzoxazole, C.I.F.B. 367 ... [Pg.136]

Other antioxidant. For example, in the case of PE, 3% by weight of carbon black is more efficient than 2,6-di-fgrt-butyl-4-methylphenol at 140°C [1]. However, the use of carbon blacks is very complicated and care must be taken against their antagonistic effect, which appears when they are combined with other antioxidants such as certain phenols or amines (diphenyl p-phenylene-diamine). [Pg.180]

Solvent extraction gas chromatographic methods have been described for determining alkylated cresols (2,6-di-tert-butyl-p-cresol) and amine antioxidants (N-phenyl-2-naphthylamine, p-phenylene diamine type) and Santoflex (NN sec-heptyl phenyl-p-phenylene diamine) in polybutadiene. [Pg.34]

The principal groups lead to the endings -diacetic acid and -di(ethylamine) , respectively, in these two cases. The central unit —Y— is cited as the bivalent radical, p-phenylene- for -C6H4- and oxy- for O. Locants are added and the full names become p-phenylenediacetic acid and 2,2 -oxydi(ethyl-amine). The parentheses in the latter name serve te remove possible confusion with a derivative of diethylamine. [Pg.46]


See other pages where Phenylene di-amines is mentioned: [Pg.764]    [Pg.322]    [Pg.322]    [Pg.561]    [Pg.561]    [Pg.562]    [Pg.575]    [Pg.575]    [Pg.575]    [Pg.575]    [Pg.764]    [Pg.322]    [Pg.322]    [Pg.561]    [Pg.561]    [Pg.562]    [Pg.575]    [Pg.575]    [Pg.575]    [Pg.575]    [Pg.421]    [Pg.366]    [Pg.119]    [Pg.541]    [Pg.149]    [Pg.612]    [Pg.342]    [Pg.119]    [Pg.374]    [Pg.2]    [Pg.3898]    [Pg.15]    [Pg.585]    [Pg.541]    [Pg.166]    [Pg.164]    [Pg.3080]    [Pg.289]    [Pg.316]    [Pg.374]   
See also in sourсe #XX -- [ Pg.561 , Pg.574 ]




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Di phenylenes

Di-amination

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