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Dicyclohexylmethane

These compounds are named as cycloalkylalkanes. Examples are dicyclohexylmethane, 1,5-dicyclopenfylpentane, l-cyclohexyl-3-(2-methylcyclohexyl)propane. [Pg.19]

Stadler IC, Karol MH. 1985. Use of dose-response data to compare the skin sensitizing abilities of dicyclohexylmethane-4,4 -diisocyanate and piciyl chloride in two animal species. Toxicol Appl Pharmacol... [Pg.179]

Imashiro et al. (3) prepared polycarbodiimides using 4,4,-dicyclohexylmethane diisocyanate terminated with moisture-resistant diisocyanates. [Pg.28]

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... [Pg.958]

Figure 7.7 SAXS profiles for two hydroxyl-terminated oligomers crosslinked by alkoxysilane sol-gel chemistry. First, 1 mole of macrodiol, SS (hydrogenated polybutadiene, HPBD or polycaprolactone, PCL, Mn= 2 kg mol-1), was reacted at 80°C with 2 mole of dicyclohexylmethane diisocyanate, H12 MDI. After complete reaction, the prepolymer was dissolved in tetrahydro-furan and the y-aminosilane, yAPS was added dropwise at room temperature. After 1 h of reaction, the solvent was removed under pressure. The final network was obtained in the absence of a solvent by hydrolysis and condensation of the ethoxysilane groups by the addition of 0.1 mol% TFA, trifluor-oacetic acid. After stirring at room temperature, the mixture was cast into a mold and cured for 24 h at 100°C under pressure, and then postcured at 150°C for 12 h. (Cuney et al., 1997 - Copyright 2001, Reprinted by permission of John Wiley Sons, Inc.)... Figure 7.7 SAXS profiles for two hydroxyl-terminated oligomers crosslinked by alkoxysilane sol-gel chemistry. First, 1 mole of macrodiol, SS (hydrogenated polybutadiene, HPBD or polycaprolactone, PCL, Mn= 2 kg mol-1), was reacted at 80°C with 2 mole of dicyclohexylmethane diisocyanate, H12 MDI. After complete reaction, the prepolymer was dissolved in tetrahydro-furan and the y-aminosilane, yAPS was added dropwise at room temperature. After 1 h of reaction, the solvent was removed under pressure. The final network was obtained in the absence of a solvent by hydrolysis and condensation of the ethoxysilane groups by the addition of 0.1 mol% TFA, trifluor-oacetic acid. After stirring at room temperature, the mixture was cast into a mold and cured for 24 h at 100°C under pressure, and then postcured at 150°C for 12 h. (Cuney et al., 1997 - Copyright 2001, Reprinted by permission of John Wiley Sons, Inc.)...
Substrate Catalyst T(° C) Solvent Ho Uptake (mol) Biphenyl or Diphenylmethane Cyclohexylbenzene or Cyclohexylphenylmethane Dicyclohexylmethane... [Pg.422]

Weyel, D.A., Schaffer, R.B. (1985). Pulmonary and sensory irritation of diphenylmethane-4,4 - and dicyclohexylmethane-4,4 -diisocyanate. Toxicol. Appl. Pharmacol. 77 427-33. [Pg.312]

DICYCLOHEXYLMETHANE-4,4 -DIISOCYANATE HYDROGENATED MDI METHYLENE BIS(4-CYCLOHEXYLISOCYANATE) (ACGIH.OSHA) NACCONATE H 12... [Pg.918]

OSHA PEL CL 0.01 ACGIH TLV TWA 0.005 ppm NIOSH REL (Dicyclohexylmethane 4,4 -diisocyanate) TWA CL 0.01 ppm SAFETY PROFILE Poison by inhalation. Mildly toxic by ingestion. When heated to decomposition it emits very toxic fumes of NOx and CN . [Pg.918]

BRN 2217800 CP 99173 Cyclohexane, 1,1 -methylenebis(4-isocyanate- Dicyclohexylmethane 4,4 -diisocyanate EINECS 225-863-2 Hydrogenated MDI Hylene W Isocyanic acid, methylenedi-... [Pg.206]

Synonyms/Trade Names Dicyclohexylmethane 4,4 -diisocyanate DMDi bis(4-isocyanatocyciohexyi)methane HMDI Hydrogenated MDI Reduced MDI Saturated MDI ... [Pg.207]

See other pages where Dicyclohexylmethane is mentioned: [Pg.307]    [Pg.307]    [Pg.156]    [Pg.373]    [Pg.199]    [Pg.27]    [Pg.190]    [Pg.216]    [Pg.218]    [Pg.322]    [Pg.313]    [Pg.307]    [Pg.307]    [Pg.307]    [Pg.1356]    [Pg.447]    [Pg.160]    [Pg.160]    [Pg.346]    [Pg.610]    [Pg.259]    [Pg.260]    [Pg.295]    [Pg.1623]    [Pg.107]    [Pg.127]    [Pg.412]    [Pg.373]    [Pg.114]    [Pg.29]    [Pg.206]    [Pg.705]    [Pg.739]    [Pg.107]    [Pg.327]    [Pg.328]   
See also in sourсe #XX -- [ Pg.4 , Pg.4 ]



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Dicyclohexylmethane diisocyanate H12MDI)

Dicyclohexylmethane-4,4 -diisocyanate

Dicyclohexylmethane-4,4 -diisocyanate HMDI)

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