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Benzothiazole sulfenamide

Af,Af-dicyclohexyl-benzothiazole-sulfenamide (DCBS), cobalt naphthenate, and diaryl-p-diphenylene-amine (each 1 phr). [Pg.256]

After reaction for 15 min, the band near 3295 cm (not shown in Fig. 13) decreased significantly in intensity, indicating that the mono-substituted acetylene groups were reacting. New bands also appeared near 1539 and 1512 cm . After reaction for 30 min, several additional bands appeared near 1011, 1030, 1085, 1232, 1320, 1430, and 1515 cm. The bands near 1011, 1030, 1085, 1232, 1320, and 1430 cm were clearly related to the benzothiazole sulfenamide fragment of DCBS while the band near 1539 cm was related to zinc stearate. [Pg.256]

The reaction with sulfides occurs efficiently only when the resulting carbon-centered radicals are further stabilized by a a-heteroatom. Indeed, (TMSfsSiH can induce the efficient radical chain monoreduction of 1,3-dithiolane, 1,3-dithiane, 1,3-oxathiolane, 1,3-oxathiolanone, and 1,3-thiazolidine derivatives. Three examples are outlined in Reaction (12). The reaction of benzothiazole sulfenamide with (TMS)3SiH, initiated by the decomposition of AIBN at 76 °C, is an efficient chain process producing the corresponding dialkylamine quantitatively. However, the mechanism of this chain reaction is complex as it is also an example of a degenerate-branched chain process. [Pg.127]

The chemical microstructures of cis-polyisoprene (HR) vulcanised with sulfur and N-t-butyl-2-benzothiazole sulfenamide (TBBS) accelerator were studied as a function of extent of cure and accelerator to sulfur ratio in the formulations by solid-state 13C NMR spectroscopy at 75.5 MHz [29]. Conventional (TBBS/Sulfur=0.75/2.38), semi-efficient (SEV=1.50/1.50) and efficient (EV=3.00/1.08) vulcanisation formulations were prepared, which were cured to different cure states according to the magnitude of increase in rheometer torque. The order and types of the sulfurisation products formed are constant in all the formulation systems with different accelerator to sulfur ratios. However, the amount of sulfurisation has been found to vary directly with the concentration of elemental sulfur. [Pg.330]

Figure 12.5a shows the effect of filler loading on the volume resistivity of MWNTs and CB (CB Ensaco 250G from Timcal) filled composites based on insulating styrene-butadiene rubber. The styrene-butadiene rubber contains 25 w% of styrene units. The microstructure of the butadiene phase is the following 10% cis, 17% trans, 73% 1,2. It was compounded with sulfur (1.1 phr), cyclohexyl benzothiazole sulfenamide (1.3 phr), diphenyl guanidine (1.45 phr), stearic acid (1.1 phr), zinc oxide (1.82 phr) (phr = parts per hundred parts of rubber). The unfilled and filled samples are cured into films (around 200 pm thick) at 170°C during 10 min under a pressure of 150 bar in a standard hot press. [Pg.351]

Sulfenamides, made from 170, by reactions involving primary and secondary amines under oxidizing conditions, include A-cyclohexyl-2-benzothiazole sulfenamide (173) and N-oxydiethylene-2-bcnzolhiazolc sulfenamide (2-(morpholinothio)benzothiazole) (174). Sulfenamides release 2-mercapto accelerators and amine during vulcanization. The amine is a secondary accelerator that brings about fast vulcanization after a slow start. Applications include in tyres and conveyor belts. They are not applicable to hot-air vulcanization processes95. [Pg.768]

Accelerators used include hexamine, diphenyl guanidine, ethylidene aniline, mercapto-benzothiazole, dibenzothiazole disulfide, N-Cyclohexyl benzothiazole sulfenamide, sodium diethyl dithiocarbamate, tetramethylthiuram disulfide, tetraethyl thiuram disulfide, dipentamethylene thiuram tetrasulfide, sodium isopropyl xanthate, zinc butyl,... [Pg.49]

Durax . [R.T. Vanderbilt] N-Cyclo-hexyl-2-benzothiazole sulfenamide rubber accelerator. [Pg.115]

Delac . [Uniroyal] Benzothiazole sulfenamides del ed-action acoelera-tor for natural and synthetic robbers used in tire treads, carcass, mechanicals, and wire jadeets. [Pg.100]

OTHER COMMENTS used as a chemical intermediate for diisopropylammonium nitrate and n,n-diisopropyl-2-benzothiazole-sulfenamide also useful as a catalyst. [Pg.571]

A[-/-butyl-2-benzothiazole sulfenamide From Afo o-Abutylamine [95-31-8] Santocuie NS, Delac NS mbber accelerator... [Pg.203]

Akrochem ZDA Powd.. See Zinc diacrylate Akrochem Accelerator BBTS. See Butyl 2-benzothiazole sulfenamide Akrochem Accelerator Bismet See Bismuth... [Pg.129]

Benzothiazol-2-ylthio) succinic acid. See 1-(Benzothiazol-2-ylthio) succinic acid Benzothiazyl-2-t-butyl sulfenamide. See Butyl 2-benzothiazole sulfenamide Benzothiazyl-2-cyclohexyl sulfenamide. See N-Cyclohexyl-2-benzothiazolesulfenamide Benzothiazyl-2-dicyclohexyl sulfenamide. See Dicyclohexylbenzothiazyl-2-sulfenamide 2-Benzothiazyl-N,N-diethylthiocarbamyl sulfide Synonyms Diethyidithiocarbamic acid-2-benzothiazoyl ester Empincal C12H14N2S3 Formula (C6H4SCN)SSCN(C2H5)2 Properties Lt. yel. to tan free-flowing powd. dens. [Pg.456]

Benzothiazyl-2-diisopropyl sulfenamide. See Diisopropyl benzothiazole sulfenamide Benzothiazyl disulfide CAS 120-78-5 EINECS/ELINCS 204-424-9 Synonyms Benzothiazole disulfide Benzothiazolyl disulfide 2-Benzothiazolyl disulfide Bis(benzothiazolyl) disulfide Di-2-benzothiazolyldisulfide Dibenzothiazyl disulfide 2,2 -Dibenzothiazyl disulfide 2,2 -Dithiobisbenzothiazole MBTS 2-Mercaptobenzothiazole disulfide 2-Mercaptobenzothiazyldisulfide Mercaptobenzthiazyl ether Empirical C14H8N2S4 Formula (C6H4SCN)2S2... [Pg.456]

BIBBS. See Di isopropyl benzothiazole, sulfenamide Bibenzal. SeeStilbene Bibenzene. See Biphenyl (A, (3H,3 H)-Bibenzo (b) thiophene)-3,3 -dione. See Thioindigo... [Pg.489]

Synonyms Benzothiazyl-2-t-butyl sulfenamide N-t-Butyl-2-benzothiazole sulfenamide TBBS Empirical C11H14N2S2 Formula C6H4NCS(SNH)C4Hg Properties Lt. buff powd. or flakes sol. in most org. soivs. m.w. 238.37 dens. 1.29 m.p. 104 C Toxicology LD50 (oral, rat) 7940 mg/kg, (IP, mouse) 5 g/kg, (IV, mouse) 180 mg/kg poison by IV route low toxicity by ing. mutagenic data TSCA listed... [Pg.606]

N-t-Butyl-2-benzothiazole sulfenamide. See Butyl 2-benzothiazole sulfenamide N-(t-Butyl) benzylamine. See N-Benzyl-N-t-butylamine... [Pg.607]

Dekacymen. See o-Cymen-5-ol Dekafald. See DMDM hydantoin Dekalin Dekalln . See Decahydronaphthalene DELA. See Diethanolamine Delac MOR. See N-Oxydiethylene benzothiazole-2-sulfenamide Delac NS. See Butyl 2-benzothiazole sulfenamide... [Pg.1186]

N,N -Dicyclohexyl-2-benzothiazole sulfenamide. See Dicyclohexylbenzothiazyl-2-sulfenamide Dicyclohexylbenzothiazyl-2-sulfenamide CAS 4979-32-2... [Pg.1285]

N,N-Diisopropyl-2-benzothiazolesulfenamide N,N-Diisopropyl benzothiazole-2-sulfenamide. See Di isopropyl benzothiazole sulfenamide Diisopropyl biphenyl. See Bis (methylethyl)-1,1 -biphenyl... [Pg.1363]

DIPA Commercial Grade, DIP A Low Freeze Grade 85 DIPA Low Freeze Grade 90 DIPA NF Grade. See Diisopropanolamine DIPA. See Diisopropylamine Diisopropyl adipate Diisopropanolamine DIPAC. See Diisopropyl benzothiazole sulfenamide Di-Pac . See Sucrose DIPA-hydrogenated cocoate Synonyms Fatty acids, coco, hydrogenated, salts with bis (2-hydroxypropyl) amine Definition Diisopropanolamine salt of hydrogenated coconut acid Uses Emulsifier, surfactant in cosmetics DIPA-lanolate... [Pg.1493]

Perkacil ETU. See Ethylene thiourea Perkacil MBS. See ISI-Oxydiethylene benzothiazole-2-sulfenamide Perkacil MBT. See 2-Mercaptobenzothiazole Perkacil MBTS. See Benzothiazyl disulfide Perkacil NDBC. See Nickel dibutyidithiocarbamate Perkacil SBEC. See Sodium dibenzyldithiocarbamate Perkacil SDBC. See Sodium di-n-butyl dithiocarbamate Perkacil SDEC. See Sodium diethyidithiocarbamate Perkacil SDMC. See Sodium dimethyidithiocarbamate Perkacii TBBS. See Butyl 2-benzothiazole sulfenamide... [Pg.3264]

TBBA-EO. See Tetrabromobisphenol A di-2-hydroxyethyl ether TBBPA. See Tetrabromobisphenol A TBBS. See Butyl 2-benzothiazole sulfenamide TBC TBC. See Tri butyl citrate 4-TBC. See t-Butylcatechol TBCH. See 3-Bromochloro-5,5-dimethyl hydantoin... [Pg.4314]


See other pages where Benzothiazole sulfenamide is mentioned: [Pg.141]    [Pg.416]    [Pg.278]    [Pg.587]    [Pg.333]    [Pg.280]    [Pg.180]    [Pg.141]    [Pg.328]    [Pg.598]    [Pg.601]    [Pg.604]    [Pg.774]    [Pg.405]    [Pg.205]    [Pg.138]    [Pg.263]    [Pg.62]    [Pg.606]    [Pg.1228]    [Pg.1363]    [Pg.2526]    [Pg.2723]   
See also in sourсe #XX -- [ Pg.595 ]

See also in sourсe #XX -- [ Pg.24 , Pg.31 , Pg.141 ]




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2- -benzothiazole sulfenamid

2- -benzothiazole sulfenamid

Benzothiazole

Benzothiazoles

Morpholinothio)-benzothiazole Sulfenamide (MBS)

N-Cyclohexyl-2-benzothiazole Sulfenamide (CBS)

N-Dicyclohexyl-2-benzothiazole Sulfenamide (DCBS)

N-f-butyl-2-benzothiazole sulfenamide

N-f-butyl-2-benzothiazole sulfenamide TBBS)

Sulfenamide

Sulfenamides

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