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2-Hydroxyethyl methyl sulfone

Purification of the crude mixture was performed by flash chromatography to afford pure 5-(l-hydroxyethyl)-2-methyl-3-furoic acid 5a-cholestan-3(3-yl ester (86% yield), 4-bromophenyl methyl sulfone (59% yield) and (R)-4-bromophenyl methyl sulfoxide (34 % yield). [Pg.112]

Thiamine stability in aqueous solution is relatively low. It is influenced by pH (Fig. 6.2), temperature (Table 6.8), ionic strength and metal ions. The enzyme-bound form is less stable than free thiamine (Fig. 6.2). Strong nucleophilic reagents, such as HS03 or OH , cause rapid decomposition by forming 5-(2-hydroxyethyl)-4-methylthiazole and 2-methyl-4-amino-5(methyl-sulfonic acid)-pyrimidine, or 2-methyl-4-amino-5-hydroxymethylpyrimidine (see Reactions 6.7). Thermal degradation of thiamine, which also initially yields the thiazole and pyrimidine... [Pg.412]

Direct sulfonation of thiazole, as well as of 2-substituted thiazoles, leads mostly to substitution m the 5-position (330-332). 4-Thiazole sulfonic acid has been prepared through direct sulfonation of 2.5-dibromothiazole with subsequent Rane% Ni reduction (330). Sulfonation of 2.5-dimethyl- and 2-piperidyl-5-methylthiazoles affords the corresponding 4-sulfonic acids as barium salts (247). The 2-hydroxy group facilitates the sulfonation (201. 236). When the 4- and 5-positions are occupied direct sulfonation can occur in the 2-position. 5-hydroxyethyl-4-methyl-2-thiazole sulfonic acid has been prepared in this manner (7). [Pg.413]

A polymeric composition for reducing fluid loss in drilling muds and well cement compositions is obtained by the free radical-initiated polymerization of a water-soluble vinyl monomer in an aqueous suspension of lignin, modified lignins, lignite, brown coal, and modified brown coal [705,1847]. The vinyl monomers can be methacrylic acid, methacrylamide, hydroxyethyl acrylate, hydroxypropyl acrylate, vinylacetate, methyl vinyl ether, ethyl vinyl ether, N-methylmethacrylamide, N,N-dimethylmethacrylamide, vinyl sulfonate, and additional AMPS. In this process a grafting process to the coals by chain transfer may occur. [Pg.46]

N-Tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid (TES) N-2-Hydroxyethylpiperazine-N -2-ethanesulfonic acid (HEPES) 3-[N,N-Bis(2-hydroxyethyl)-amino]-2-hydroxypropane-sulfonic acid (DIPSO) 3-[N-Tris(hydroxymethyl)-methylamino-2-hydroxy-propanesulfonic acid (TAPSO) N-(2-Hydroxyethyl)piperazine-N -(2-hydroxypropanesulfonic acid) (HEPPSO)... [Pg.323]

In the tenth official proficiency test, the presence of bis(2-hydroxyethyl) sulfone) (BHES, CAS 2580-77-0) in the decontamination solution sample D2 was missed by one laboratory. The laboratory performed liquid-liquid extraction of the aliquots with dichloromethane and benzene, concentrated the organic extracts, and silylated them. One aliquot of the organic extract was evaporated to dryness, dissolved, methylated, evaporated to dryness, and dissolved again. Evaporation of the water phase to dryness and silylation of the residue was not reported, and the failure to do this might be the reason why the laboratory did not identify BHES using GC-based methods for analysis. [Pg.178]

Many approaches have been developed for the production of ionic liquid-polymer composite membranes. For example, Doyle et al. [165] prepared RTILs/PFSA composite membranes by swelling the Nafion with ionic liquids. When 1-butyl, 3-methyl imidazolium trifluoromethane sulfonate was used as the ionic liquid, the ionic conductivity ofthe composite membrane exceeded 0.1 S cm at 180 °C. A comparison between the ionic liquid-swollen membrane and the liquid itself indicated substantial proton mobility in these composites. Fuller et al. [166] prepared ionic liquid-polymer gel electrolytes by blending hydrophilic RTILs into a poly(vinylidene fiuoridej-hexafluoropropylene copolymer [PVdF(HFP)] matrix. The gel electrolytes prepared with an ionic liquid PVdF(HFP) mass ratio of 2 1 exhibited ionic conductivities >10 Scm at room temperature, and >10 Scm at 100 °C. When Noda and Watanabe [167] investigated the in situ polymerization of vinyl monomers in the RTILs, they produced suitable vinyl monomers that provided transparent, mechanically strong and highly conductive polymer electrolyte films. As an example, a 2-hydroxyethyl methacrylate network polymer in which BPBF4 was dissolved exhibited an ionic conductivity of 10 S cm at 30 °C. [Pg.357]

Monomers 4VP, 4-vinylpyridine NIPAAm, jV-isopropylacrylamidc AA, acrylic acid PEGMA, poly (ethylene glycol) methacrylate SPE, MAI-dimethyl-AW2-methacryloyloxycthyl-/V-0-sulfopropyl)amm<>-nium betaine AMPS, 2-acrylamido-2-methyl-l-propanesulfonic acid qDMAEMA, quaternary 2-dimethylaminoethyl methacrylate St, styrene HEMA, 2-hydroxyethyl methacrylate HEA, 2-hydro-xyethyl acrylate DMAEMA, 2-dimethylaminoethyl methacrylate MAA, methacrylicacid NaSS sodium p-styrene sulfonate AC, [(2-acryloyloxy)ethyl]trimethyl ammonium chloride GMA, glycidyl methacrylate NVP, jV-vinylpyrrolidone MAn, maleic anhydride BVE n-butyl vinyl ether AAm, acrylamide DEAAm, MA-diethylacrylamidc DMAAm, MA -dimethylacrylamidc MMA, methyl methacrylate. [Pg.532]

The active substance is not toxic to mammals, the acute oral ld,o for male rats is 4900 mg/kg. The active substance is rapidly absorbed and metabolised in the animal. It is excreted in the urine and feces, llie following metabolites have been detected in the urine p-(l,l-dimethyl-2-hydroxyethyl)benzylmethyl sulfide and sulfone, and p-(l-methyl-l-carboxyethyI)benzyImethyl sulfide and sulfone and their glucuronide conjugates. In addition to these, butyl-(l,I-dimethyl-2-hydroxyethyl)benzyl-N-(3-pyridyl)dithiocarbonimidate has been detected in the feces (Ohkawa et al., 1975). [Pg.455]

Aerosol OT-100% Methyl hydroxyethyl-cellulose Monawet MT-70E Nonoxynol-9 Tylose MH Grades Tylose MHB dispersant, suspension polymerizations Luviskol K17 Luviskol K30 Luviskol K60 Luviskol K90 dispersant, synthetic latex Sodium polynaphthalene sulfonate dispersant, synthetic polymers Daxad 11G... [Pg.1508]

Bis (2-hydroxyethyl) octyl methyl ammonium p-toluene sulfonate CAS 58767-50-3... [Pg.516]

Octanamine, N-octyl. See Dioctyl amine 1 -Octanaminium, N,N-bis(2-hydroxyethyl)-N-methyl-, salt with 4-methylbenzenesulfonic acid (1 1). See Bis (2-hydroxyethyl) octyl methyl ammonium p-toluene sulfonate Octanaminium, N,N-dimethyl-N-octyl-, chloride. See Dioctyl dimonium chloride 1-Octanaminium, N-methyl-N,N-dioctyl-, chloride. See Tricaprylyl methyl ammonium chloride... [Pg.2926]

Ammonium lauryl sulfate Ammonium polyaspartate Calcium dodecylbenzene sulfonate CIO-12 pareth-5 Cl2-14 pareth-8 Cl 2-14 pareth-9 Cl 2-15 pareth-7 Cl 2-15 pareth-8 Cl 3-15 pareth-20 lsodeceth-4 Lauryl hydroxyethyl imidazoline Methyl hydroxyethylcellulose Nonoxynol-12 Nonoxynol-20 Octoxynol-6 Oleth-2 PEG-5 castor oil PEG-26 castor oil PEG-180 castor oil PEG-8 cocoate PEG-20 hydrogenated castor oil PEG-2 hydrogenated tallowamine PEG-20 hydrogenated tallowamine PEG-60 hydrogenated tallowate PEG-9 laurate PEG-2 oleamine PEG-7 oleamine PEG-9 oleate PEG-12 ricinoleate PEG-10 stearamine PEG-2 stearate PEG-8 tallate PEG-12 tallate Polysorbate 81 PPG-20 lanolin alcohol ether... [Pg.5112]

Ammonium nonoxynol-4 sulfate Ammonium nonoxynol-6 sulfate Ammonium phosphate Antimony trichloride Butylated PVP Ceteareth-4 Ceteareth-6 Ceteareth-8 Ceteareth-10 Ceteareth-11 Ceteareth-14 Ceteareth-18 Ceteareth-80 Chitosan Chloro-2-hydroxypropyl trimonium chloride Cyanamide-formaldehyde resin Dibehenyidimonium chloride Diethylene glycol Disodium arsenate Hydrogenated tallowalkonium chloride Hydroxylamine sulfate lsodeceth-6 Lauryl hydroxyethyl imidazoline Lysolecithin MEA-dodecylbenzene sulfonate Octoxynol-25 Oleth-18 Oxalic acid dihydrate PCA PEG-80 castor oil PEG lauramine PEG laurate PEG-20 laurate PEG-14 oleate PEG-5 stearate PEG-23 stearate PEG-8 tallate Potassium acid tartrate Sodium arsenate Sodium chromate Sodium dodecyl diphenyloxide disulfonate Sodium methyl oleoyl taurate Sodium methyl tallow taurate Sodium sulfate... [Pg.5139]


See other pages where 2-Hydroxyethyl methyl sulfone is mentioned: [Pg.83]    [Pg.1982]    [Pg.83]    [Pg.1982]    [Pg.1038]    [Pg.266]    [Pg.148]    [Pg.17]    [Pg.236]    [Pg.369]    [Pg.115]    [Pg.194]    [Pg.57]    [Pg.559]    [Pg.217]    [Pg.368]    [Pg.296]    [Pg.243]    [Pg.2]    [Pg.544]    [Pg.301]    [Pg.644]    [Pg.648]    [Pg.44]    [Pg.1501]    [Pg.1526]    [Pg.2160]    [Pg.5770]    [Pg.5846]    [Pg.957]   
See also in sourсe #XX -- [ Pg.83 ]




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Hydroxyethylation

Methyl sulfone

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