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I Chloroform

Pillai, C.G.P., J.D. Weete, and D.E. Davis. 1977. Metabolism of atrazine by Spartina altemiflora. I. Chloroform-soluble metabolites. Jour. Agric. Food Chem. 25 852-855. [Pg.801]

Fig. 11. Low-resolution HPLC chromatograms of ZK32347. a water/methanol, 650 80 (v/v). b water/methanol, 650 80 (v/v)-i-chloroform (8 g L 0... Fig. 11. Low-resolution HPLC chromatograms of ZK32347. a water/methanol, 650 80 (v/v). b water/methanol, 650 80 (v/v)-i-chloroform (8 g L 0...
Solvent I (chloroform-methanol 1 1, v/v). In 10 column volumes, all of the choline-containing phospholipids should have passed through. Then, start the following ... [Pg.55]

Scheme 8, Reagents i, chloroform, NaOH (50%), tetra-n-butylammonium chloride ii, methanol, sodium carbonate iii, toluene, reflux iv, LiAlH4, AICI3, tetrahydrofuran v, H2, 10% Pd/C, sodium acetate, ethanol. Scheme 8, Reagents i, chloroform, NaOH (50%), tetra-n-butylammonium chloride ii, methanol, sodium carbonate iii, toluene, reflux iv, LiAlH4, AICI3, tetrahydrofuran v, H2, 10% Pd/C, sodium acetate, ethanol.
Fig.3 Coexistence curve of the system tri-methyl-ethylammonium bromide -i- chloroform in the presence of 1% ethanol. The arrow indicates the CP. Fig.3 Coexistence curve of the system tri-methyl-ethylammonium bromide -i- chloroform in the presence of 1% ethanol. The arrow indicates the CP.
With fuming HNO, a yellow color, and when shaken wi i chloroform the IfUter is colored violet or colors starch-paste dark blue,... [Pg.113]

I) Chloroform contains C-H bonds which would absorb In the same region as the hydrocarbons. CF3CCI3 contains no C-H bonds. [Pg.451]

Problem 8.4 Use the data below for the system ethyl propyl ether (i)-chloroform (2) to answer the following questions ... [Pg.334]

The excess free enthalpy of mixing for the binary system ethanol (I)-chloroform (2) at 50°C for three different compositions is given below ... [Pg.153]

Solvent I = Chloroform-analytical grade, standard conditions, CS II = n-hexane-ethyl acetate (90 -f 10), standard conditions, NS III = benzene-methanol (75 + 25), layer prepared according to [196] IV = benzene-methanol (95 + 5), layer prepared according to [196] hi /-values to be regarded only as guide values. [Pg.226]

Fig. 150. Thin-layer chromatogram of phospholipids and other polar lipids of bovine milk [159 a]. 1 carbohydrate (lactose) and protein, 2 sphingomyelin, 3 phosphatidyl choline, 4 phosphatidyl serine, 5 phosphatidyl inositol, 6 phosphatidyl ethanolamine, 7 cerebroside dihexoside ( ), 8 cerebroside mono-hexoside ( ), P fatty acids, 10 neutral lipids. Adsorbent Silica gel HR. Solvents I, chloroform-methanol-water-28% aqu. ammonia (130 + 70+8 + 0.5) II, chloroform-acetone-methanol-acetic acid-water (50 + 20 + 10 + 10 + 5). Time 40 min in each direction. Indicator charring with chromic sulphuric acid solution... Fig. 150. Thin-layer chromatogram of phospholipids and other polar lipids of bovine milk [159 a]. 1 carbohydrate (lactose) and protein, 2 sphingomyelin, 3 phosphatidyl choline, 4 phosphatidyl serine, 5 phosphatidyl inositol, 6 phosphatidyl ethanolamine, 7 cerebroside dihexoside ( ), 8 cerebroside mono-hexoside ( ), P fatty acids, 10 neutral lipids. Adsorbent Silica gel HR. Solvents I, chloroform-methanol-water-28% aqu. ammonia (130 + 70+8 + 0.5) II, chloroform-acetone-methanol-acetic acid-water (50 + 20 + 10 + 10 + 5). Time 40 min in each direction. Indicator charring with chromic sulphuric acid solution...
Solvent I = Chloroform-methanol-ammonium hydroxide (60 + 10 + 1) II = chloroform-methanol-acetic acid (60 + 10 + 1)... [Pg.431]

Solvent I = Chloroform-ethyl acetate (60 -f 60) II = Ethyl acetate-absolute ethanol (76 + 26) III = Ethyl acetate-absolute ethanol (50 + 60) IV = Pure ethyl acetate. [Pg.450]

Solvents I Chloroform-acetone (90+ 10) II Benzine (Swiss Pharmacopoeia)-dioxan (75 + 30) III Benzene-ether (50 + 50). [Pg.538]

Solvents I = Chloroform-methanol (90 + 10) II = Benzene-acetic acid (90 + 10) m = Hexane-diethyl ether (90 + 10) IV = Hexane-acetic acid (90 + 10) V = Methylcyclohexane, used on an alumina layer which had been impregnated with a 20% solution of dimethylf ormamide in diethyl ether VI = Benzene VII = Acetone VIII = Ethyl acetate IX = Isopropanol X = Methanol. [Pg.642]


See other pages where I Chloroform is mentioned: [Pg.751]    [Pg.223]    [Pg.417]    [Pg.170]    [Pg.271]    [Pg.1185]    [Pg.39]    [Pg.631]    [Pg.424]    [Pg.271]    [Pg.1727]    [Pg.277]    [Pg.137]    [Pg.374]    [Pg.191]    [Pg.281]    [Pg.365]    [Pg.99]    [Pg.99]    [Pg.365]    [Pg.433]    [Pg.439]    [Pg.443]    [Pg.448]    [Pg.453]    [Pg.535]    [Pg.775]    [Pg.120]    [Pg.130]    [Pg.162]    [Pg.193]    [Pg.315]    [Pg.32]   
See also in sourсe #XX -- [ Pg.65 ]




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I-Butyl chloroformate

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