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Triallyl ester

Curing of multicomponent systems consisting of BPA/DC, BMI and diallyl or triallyl esters (triallyl isocyanurate TAIC in particular) results in high Tgvalues. Such compositions consist of BPA/DC, BMI, TAIC, diallyl phthalate and dicumyl peroxide [127], BPA/DC prepolymer, BMI, TAIC, /erf.butyl peroxide, Zn acetate and DABCO [128] or BMI/trimethylene bis(4-aminobenzoate) prepolymer, BPA/DC, Zn octoate and TAIC [129]. [Pg.56]

Beilstein Handbook Reference) Activator OC Ai3-26448 BRN 0235560 Cyanuric acid, tri-2-propenyi ester Cyanuric acid triallyl ester EINECS 202-936-7 NSC 4804 Perkalink 300 Perkalink 300-50D Rhenofit TAC TAG Triallyl cyanurate Tripropargyl cyanurate 2,4,6-Tri(allyloxy)-s-triazine 2,4,6-Triallyloxy-1,3,5-triazine 1,3,5-Triazine, 2,4,6-tris(2-propenyloxy)- s-Triazine, 2,4,6-tris(allyloxy)- 2,4,6-Triprop-2-ynyloxy-s-triazine ... [Pg.629]

Beilstein Handbook Reference) AI3-60290 BRN 0225482 CCRIS 6105 DIAK 7 EINECS 213-834-7 Isxyanuric acid triallyl ester NSC 11692 TAIC Triallyl isocyanurate 1,3,5-Triallyl-1,3,5-triazine-2.4,6 1H,3H,5H)-trione 1,3,5-Triallyl... [Pg.629]

Benzenetricarboxylic acid, tri-2-propenyl ester 1,2,4-Benzenetricarboxylic acid, triallyl ester EINECS 220-264-2 Sipomer TATM TATM Triallyl benzene-1,2,4-tricarboxylate Triallyl trimellitate 1,2,4-Triallyl trimellitate Triam 705 Trimellitic acid triallyl ester. Liquid mp = -30" bp4 = 210" d = 1.160. Rhone Poulenc Surfactants. [Pg.630]

Trimeilitic acid triallyl ester 3838 Trioleate de sorbitano 3540... [Pg.1114]

Triallyl esters impart a greater degree of cross-linking than diallyl esters and are therefore used as hardening agents. Triallyl cyanurate forms ex-... [Pg.1027]

Isocyanuric acid, dichloro-. See Dichloroisocyanuric acid Isocyanuric acid, dichloro-, potassium salt. See Potassium dichloroisocyanurate Isocyanuric acid triallyl ester. See Triallyl isocyanurate... [Pg.2220]

Phosphoric acid, triallyl ester. SeeTriallyl phosphate. [Pg.3348]

CAS 1025-15-6 EINECS/ELINCS 213-834-7 Synonyms Isocyanuric acid triallyl ester TAIC ... [Pg.4469]

For this reason, only di- and triallyl monomers have achieved commercial significance, and then only the esters. Since the cross-linked polymer occurring in this polymerization involves the side chains containing ester groups, they are also sometimes referred to industrially as polyesters. The di- and triallyl ester monomers are produced by the reaction of allyl alcohol with acids, acid anhydrides, or acid chlorides. Examples of monomers are diallyl phthalate (1) from phthallic anhydride, and triallyl cyanurate (II) from trichloro-5-triazine ... [Pg.439]

In addition to diolefins, there are other bifunctional compounds that will form boron heterocyclics under analogous reaction conditions. For example, the triallyl ester of orthoboric acid reacts with trialkylamine-borane in the presence of trialkylboranes to give B-alkyl-l,2-oxaborolane (XXXVIII) (5). [Pg.277]

See other pages where Triallyl ester is mentioned: [Pg.1008]    [Pg.985]    [Pg.1259]    [Pg.629]    [Pg.879]    [Pg.974]    [Pg.158]    [Pg.159]    [Pg.150]    [Pg.151]    [Pg.45]    [Pg.463]    [Pg.927]    [Pg.137]    [Pg.181]    [Pg.182]    [Pg.164]    [Pg.169]    [Pg.180]    [Pg.150]   
See also in sourсe #XX -- [ Pg.4 ]



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Triallyl

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