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Compounding conditions

Nitro compound Aza compound Conditions Relative rate, N02/aza Reference... [Pg.320]

Si-H containing functional initiators have been obtained by reduction with LAH of the corresponding Si-Cl containing compounds. Conditions have been developed under which the benzylic chloride remains unchanged while the Si-Cl bond is converted to Si-H (for experimental details see Sect. H.C.). The initiators obtained are shown in Table 1. [Pg.21]

Nitro compound compound Condition Product (synJanti) Ref. [Pg.34]

Entry Starting compound Conditions Product Reference... [Pg.735]

Fig. 3.158. Electropherogram of a 10-compound aromatic sulphonate mixture containing 2 mg/1 of each compound. Conditions running electrolyte 12 mM sodium borate, pH 9.3, capillary 47 cm (40 cm to detectiom window) X 75 pm i.d., voltage 25 kV, temperature 25°C, pressure injection 0.5 psi. for 5 s, UV detection at 214 nm. For peak identification see Table 3.44. Reprinted with permission from R. Loos et al. [197]. Fig. 3.158. Electropherogram of a 10-compound aromatic sulphonate mixture containing 2 mg/1 of each compound. Conditions running electrolyte 12 mM sodium borate, pH 9.3, capillary 47 cm (40 cm to detectiom window) X 75 pm i.d., voltage 25 kV, temperature 25°C, pressure injection 0.5 psi. for 5 s, UV detection at 214 nm. For peak identification see Table 3.44. Reprinted with permission from R. Loos et al. [197].
Compound Conditions (h, rt) Product Yield (%) Empirical formula... [Pg.346]

Figure 7.4 Analytical separation of a regioisomer mixture with a resolution of 1.78. The first peak is the desired compound. Conditions feed concentration 20 mg/ml injection volume 5 (il Kromasil KR100-10-C18, 250 X 4.6 (i.d.) mm flow rate 1.0 ml/min 80/20 (v/v) acetonitrile/water UV 254 nm. Figure 7.4 Analytical separation of a regioisomer mixture with a resolution of 1.78. The first peak is the desired compound. Conditions feed concentration 20 mg/ml injection volume 5 (il Kromasil KR100-10-C18, 250 X 4.6 (i.d.) mm flow rate 1.0 ml/min 80/20 (v/v) acetonitrile/water UV 254 nm.
With aromatic compounds conditions can be found so that ring oxidation predominates and phenolic compounds are formed. Benzene is oxidized quantitatively to phenol. Toluene is oxidized to o-cresol, m-xy-lene to l,3-xylen-4-ol, and naphthalene to f-naphthol. The addition of certain additional catalyst, such as molybdenum oxide, promoted coupling reactions and biphenyl was formed from benzene, bi- or poly-tolyl hydrocarbons from toluene, di- and polyxylyls from wi-xylene, and a... [Pg.222]

Compound Conditions" Time for complete hydrolysis0 (minutes)... [Pg.65]

Compound Condition of Stainless Steel Surface Spontaneous Ignition Temp., ° F. [Pg.231]

Figure 3. Acidolysis of arylglycerol -aryl ether model compounds. Conditions 0.2M HCl in dioxane-water, 9 1, refluxed for 4 hours. Figure 3. Acidolysis of arylglycerol -aryl ether model compounds. Conditions 0.2M HCl in dioxane-water, 9 1, refluxed for 4 hours.
Compound Condition Year 1 Year 2 Year 1 Year 2... [Pg.283]

Porapak-QS 250 Ethylvinyl benzene-divinyl benzene copolymer 625 525 565 445 Similar to Porapak-Q at lower operating temperatures, but useful for higher-molecular-weight solutes Silanized Porapak-Q reduces tailing of high-polarity compounds condition at 250° C... [Pg.48]

TABLE 1 Dimerization of Cinnamic Acids as Monitored by Powder X-ray Diffraction Compound/conditions... [Pg.222]

Tellurium Compound Metal Compound Conditions Complex Refer- ence... [Pg.459]

EPA currently uses the heat of combustion to rank the incinerability of hazardous compounds, although kinetics, not thermodynamics, govern incinerator performance. More important, because of interactions between species, rates of reaction of hazardous compounds in a mixture can be considerably different from those observed under single-compound conditions. Moreover, the hydrocarbon fuels used to cofire the incinerator can interact with the hazardous substances themselves. [Pg.288]

Aidoi reactions with highly enolizabie compounds 1,3-Dlcarbonyl compound Conditions... [Pg.719]

Figure 1 Influence of pH on migration times of purine compounds. Conditions capillary, 44 cm (37 cm to detector) x 75 pm i.d. buffer, 20 mM borate voltage, 20 kV temperature, 37°C detection, UV, 254 nm. Key = adenine, + = adenosine, = guanine, x=guanosine, = hypoxanthine, A=xanthine, X = uric acid. (Reprinted from Ref. 1 3 with permission of Elsevier Science Publishers.)... Figure 1 Influence of pH on migration times of purine compounds. Conditions capillary, 44 cm (37 cm to detector) x 75 pm i.d. buffer, 20 mM borate voltage, 20 kV temperature, 37°C detection, UV, 254 nm. Key = adenine, + = adenosine, = guanine, x=guanosine, = hypoxanthine, A=xanthine, X = uric acid. (Reprinted from Ref. 1 3 with permission of Elsevier Science Publishers.)...
Copper compound" Conditions Temp. Oxidant (°C) Dimer yield (%) References... [Pg.256]


See other pages where Compounding conditions is mentioned: [Pg.111]    [Pg.330]    [Pg.32]    [Pg.265]    [Pg.270]    [Pg.101]    [Pg.79]    [Pg.274]    [Pg.397]    [Pg.178]    [Pg.2]    [Pg.43]    [Pg.125]    [Pg.138]    [Pg.128]    [Pg.142]    [Pg.144]    [Pg.111]    [Pg.29]    [Pg.36]    [Pg.43]    [Pg.46]    [Pg.19]    [Pg.74]    [Pg.190]    [Pg.178]   
See also in sourсe #XX -- [ Pg.476 ]




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Anaerobic conditions organic compounds

Aromatic carbonyl compounds reducing conditions

Carcinogenic compounds under experimental conditions

Compound Distribution Depends on Reaction Conditions

Compound surfaces under growth condition

Compounding process conditions

Labile compounds, preparation under protective conditions

Phenolic compounds chromatographic conditions

Preparation of Labile Compounds under Protective Conditions. Chromium (II) Salts

Reissert compounds under acidic conditions

Role of the Mixing Equipment and Compounding Conditions

Sulfur compounds formed from conditions

The interaction of an alcohol with a halogen compound under basic conditions

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