Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Clear Light

A mixture of 0.10 mol of freshly distilled 3-methyl-3-chloro-l-butyne (see Chapter VIII-3, Exp. 5) and 170 ml of dry diethyl ether was cooled to -100°C and 0.10 mol of butyllithium in about 70 ml of hexane was added at this temperature in 10 min. Five minutes later 0.10 mol of dimethyl disulfide was introduced within 1 min with cooling betv/een -100 and -90°C. The cooling bath vjas subsequently removed and the temperature was allowed to rise. Above -25°C the clear light--brown solution became turbid and later a white precipitate was formed. When the temperature had reached lO C, the reaction mixture was hydrolyzed by addition of 200 ml of water. The organic layer and one ethereal extract were dried over potassium carbonate and subsequently concentrated in a water-pump vacuum (bath... [Pg.75]

Modified MDI s Urethane-modified 2.0 Clear, light yellow Flexible, 2-K structural adhesive... [Pg.768]

Observable Characteristics - Physical State (as shipped) Liquid Color Colorless clear, lightly colored Odor. None slight sweet faint ether-like. [Pg.322]

Helltran, m. a clear, light yellow fish oil. hellweiss, a. clear white, bright white. [Pg.210]

The solvent was evaporated from the combined benzene extracts to give 33.4 g of a clear light brown resin. Crystallization from an alcohol-water mixture gave 19.5 g of 1-methyl-4-(5-hydroxy-5-dibenzo[a,e] cycloheptatrienyO-piperidine, MP 156° to 157°C. Two recrystallizations from alcohol-water mixtures followed by two recrystallizations from benzene-hexane mixtures gave analytically pure product, MP 166.7° to 167.7°C. [Pg.421]

It is not necessary that the intermediate be separated from the reaction medium in the preparation of the end product. Instead, the reaction mixture, after cooling, is treated with 200 ml of water acidified with 42 ml 10% hydrochloric acid solution, and filtered. To the clear, light yellow filtrate is added dropwise a solution of 9.B g (0.07 mol) 5-nltro-2-furaldehyde in 100 ml ethyl alcohol. An orange solution of the hydrochloride results. The free base is precipitated asyellow plates by making the solution basic with saturated sodium carbonate solution. 14 g of the compound is filtered off by suction, washed with alcohol, and dried. The yield, MP 204°C to 205°C (dec.), is 53% of theoretical based on 3-(N-morpholinyl)-1,2-epoxy-propane. Recrystallization from 95% alcohol (75% recovery) raises the melting point to 206°C (dec.). [Pg.707]

In summary, although clear, light-colored cellulose solutions are required to start the synthesis, there is no guarantee, a priori, that the targeted DS will be obtained. The reasons are that the state of aggregation of cellulose is dependent on the structural characteristics of the starting material, is sensitive to the pre-treatment employed, and the impurities present. This may result in non-reproducible aggregation states, and may lead to oscillation in cellulose reactivity. Typically, effects of these oscillations may not be readily apparent, because ... [Pg.122]

Decanters are used to separate liquids where there is a sufficient difference in density between the liquids for the droplets to settle readily. Decanters are essentially tanks which give sufficient residence time for the droplets of the dispersed phase to rise (or settle) to the interface between the phases and coalesce. In an operating decanter there will be three distinct zones or bands clear heavy liquid separating dispersed liquid (the dispersion zone) and clear light liquid. [Pg.440]

The mixture is then chilled in an ice bath for at least 3 hours, and the olive-brown precipitate of the sparingly soluble copper complex of imidazole derivatives is filtered. The product is washed with about 500 ml. of cold water, suspended while moist (Note 4) in 11. of water, and rendered just acid to litmus by the addition of concentrated hydrochloric acid (about 40 ml.). Hydrogen sulfide is then passed into the suspension, with frequent shaking, until precipitation of the copper is complete (2-3 hours). The precipitate is filtered and extracted with 500 ml. of hot water in two or three portions. The clear, light brown to reddish brown filtrate and washings are boiled for 15 minutes, and then 60 g. (0.26 mole) of picric acid is added with stirring heating is continued until solution is complete. [Pg.95]

Turanose Phenylosotriazole. A solution of 15 g. of turanose phenylosazone in 300 cc. of hot water was placed on the steam-bath and a solution of 22 g. of copper siilfate pentahydrate in 150 cc. of hot water was added. The mixture turned a deep cherry-red at once and in a short time (fifteen min.) a red precipitate had formed and the solution had become green. After thirty minutes from the time of addition of the copper solution, the solution was cooled, filtered, and the copper removed as sulfide. The clear light yellow filtrate was neutralized with 45 g. of barium carbonate and the insoluble material removed by filtration. The filtrate was extracted with five 50-cc. portions of ether to remove the aniline, and the aqueous portion was concentrated in vacuo to a thick sirup. The sirup was dissolved in 60 cc. of warm alcohol, filtered to remove a slight turbidity and diluted with 65 cc. of ether. Upon cooling and scratching, the product crystallized as large prisms yield 8.9 g. (72%). The phenylosotriazole was recrystallized from 10 parts of alcohol and when pure showed the melting point 193-194° and rotated [a Jj" + 74.5° in aqueous solution (c, 0.90). [Pg.45]

A Hunter Color and Color Difference Meter was used to evaluate flour color. The effect of roasting condition on Hunter L values of flours indicated that lightness values (L) decreased with increased roasting temperature and time with all navy bean cotyledonary fractions possessing a clear light appearance. [Pg.195]

Clear, light colored, viscous, oily liquid with a slight odor... [Pg.516]

Clear, light yellow to brown, oily liquid with an almond-like or shoe polish odor. May darken on exposure to air. An experimentally determined odor threshold concentration of 4.7 ppbv was reported by Leonardos et al. (1969). A detection odor threshold concentration of 9.6 mg/m (1.9 ppmv) was determined by Katz and Talbert (1930). [Pg.841]

Appearance Clear, light yellow Viscosity <10 cps Specific Gravity 1.03 pH (as is) <1.0... [Pg.3]

Appearance Clear, light yellow liquid Specific Gravity 1.00 Viscosity <10 cps pH, as is 9.5... [Pg.90]

High-Foaming. Clear. Light-Dutv Liquid Cleaner... [Pg.101]

Physical Appearance Clear light amber liquid... [Pg.204]


See other pages where Clear Light is mentioned: [Pg.98]    [Pg.100]    [Pg.516]    [Pg.66]    [Pg.52]    [Pg.50]    [Pg.73]    [Pg.972]    [Pg.1087]    [Pg.624]    [Pg.112]    [Pg.356]    [Pg.567]    [Pg.26]    [Pg.135]    [Pg.144]    [Pg.202]    [Pg.221]    [Pg.282]    [Pg.111]    [Pg.63]    [Pg.22]    [Pg.236]    [Pg.80]    [Pg.102]    [Pg.183]   
See also in sourсe #XX -- [ Pg.135 ]

See also in sourсe #XX -- [ Pg.62 , Pg.77 ]




SEARCH



Clear

Clearness

© 2024 chempedia.info