Isopropyl alcohol, extraction

Proc Okla Acad Sci 1974 54 34-35. Demole, E., and C. Demole. A chemical study of hurley tobacco flavour Nicotiarui tabacum). VII. Identification and synthesis of twelve irregular terpenoids related to solanone, including 7,8-dioxabicycIo[3,2,l]-octane and 4,9-dioxabicycIo[3.3.1 Jnonane derivatives. Helv Chim Acta 1975 58 1867. Bharadwaj, B. V., S. Takayama, T. Yamada, and A. Tanimura. N -nitro-sonornicotine in Japanese tobacco products. Gann 1975 66 585. Randolph, H. R. Gas chromatographic determination of nicotine in an isopropyl alcohol extract of smoke particulate matter. Tobacco 1974 176 44-Yung, K. H., and D. H. Northcote. Enzymes in the walls of mesophyll cells of tobacco leaves. Biochem J 1975 151 141. 

Figure 9. Two-dimensional cellulose TLC of flavonoids in aqueous isopropyl alcohol extracts, nonflavonoid fractions of extracts, and flavonoid fractions of extracts of LCP and glandless cottonseed flours (5)...

Randolph, H.R. A gas chromatographic determination of nicotine from an isopropyl alcohol extract of TPM 27th Tobacco Chemists Research Conference, Program Booklet and Abstracts, Vol. 27, Paper No. 19, 1973, p. 12 A gas chromatographic determination of nicotine in an isopropyl alcohol extract of smoke particulate matter Tob. Sci. 18(1974) 133-135. 

Isopropyl alcohol extracts of the sponge Tethya aurantia were fractionated for a component with negative chronotropic and inotropic activity on isolated guinea pig atria 181). The bioactive substance was found to be adenosine. The extracts also contained allantoin (293), which is an intermediate in the purinolytic sequence. Dichloromethane and methanol extracts of a new species of the genus Echinodictyum showed strong activities on the isolated guinea-pig trachea 182). The active constituent was identified as 4-amino-5-bromopyrrolo[2,3-d]pyr-imidine (294). 

Sodium hydride (9.3 g, 0.22 mol) was washed with petroleum ether and DMSO (200 ml) was added and the mixture was heated to 100°C. A solution of diethyl malonate (35.2 g, 0.22mol) in DMSO (50 ml) was then added and stirred for 10 min to give a clear solution. A solution of 4-bromo-3-nitrobenzophenone (30.6 g, 0.10 mol) in DMSO (100 ml) was added and the resulting dark solution kept at 100 C for 1 h. The solution was poured into water (3 1) and extracted (2x) with ether. The extract was washed with water, dried (NajSOj and concentrated in vacuo to give an oil which crystallized. The solid was recrystallized from isopropyl alcohol to give 35.4 g (92% yield) of the product. 

Either product can be favored over the other by proper selection of catalyst and reaction conditions. However, the principal source of DIPE is as a by-product from isopropyl alcohol production. Typically, excess DIPE is recycled over acidic catalysts ia the alcohol process where it is hydrated to isopropyl alcohol. DIPE is used to a minor extent ia iadustrial extraction and as a solvent. 

An hplc assay was developed suitable for the analysis of enantiomers of ketoprofen (KT), a 2-arylpropionic acid nonsteroidal antiinflammatory dmg (NSAID), in plasma and urine (59). Following the addition of racemic fenprofen as internal standard (IS), plasma containing the KT enantiomers and IS was extracted by Hquid-Hquid extraction at an acidic pH. After evaporation of the organic layer, the dmg and IS were reconstituted in the mobile phase and injected onto the hplc column. The enantiomers were separated at ambient temperature on a commercially available 250 x 4.6 mm amylose carbamate-packed chiral column (chiral AD) with hexane—isopropyl alcohol—trifluoroacetic acid (80 19.9 0.1) as the mobile phase pumped at 1.0 mL/min. The enantiomers of KT were quantified by uv detection with the wavelength set at 254 nm. The assay allows direct quantitation of KT enantiomers in clinical studies in human plasma and urine after adrninistration of therapeutic doses. 

Paprika oleoresin (EEC No. E 160c) is the combination of davor and color principles obtained by extracting paprika with any one or a combination of approved solvents acetone, ethyl alcohol, ethylene dichloride, hexane, isopropyl alcohol, methyl alcohol, methylene chloride, and trichloroethylene. Depending on their source, paprika oleoresins are brown—red, slightly viscous, homogeneous Hquids, pourable at room temperature, and containing 2—5% sediment. 

Com endosperm oil—A reddish brown Hquid composed chiefly of glycerides, fatty acids, sitosterols, and carotenoid pigments obtained by isopropyl alcohol and hexane extraction from the gluten fraction of yellow com grain. 

Stratifying water systems for selective extraction of thiocyanate complexes of platinum metals have been proposed. The extraction degree of mthenium(III) by ethyl and isopropyl alcohols, acetone, polyethylene glycol in optimum conditions amounts to 95-100%. By the help of electronic methods, IR-spectroscopy, equilibrium shift the extractive mechanism has been proposed and stmctures of extractable compounds, which contain single anddouble-chai-ged acidocomplexes [Rh(SCN)J-, [Ru(SCN)J, [Ru(SCN)J -have been determined. Constants of extraction for associates investigated have been calculated. 

While keeping the collected deuterioammonia at dry ice-isopropyl alcohol temperature, lithium wire (10 mg) is added, followed by a solution of 3/3-hydroxy-5a-cholest-7-en-6-one (161 50 mg) in anhydrous tetrahydrofuran (4 ml). The reaction mixture is stirred for 20 min, the cooling bath is then removed and the ammonia is allowed to boil under reflux for 40 min. A saturated solution of ammonium chloride in tetrahydrofuran is added dropwise until the deep blue color disappears and then the ammonia is allowed to evaporate. The residue is extracted with ether and the organic layer washed with dilute hydrochloric acid and sodium bicarbonate solution and then with water. Drying and evaporation of the solvent gives a semicrystalline residue which is dissolved in acetone and oxidized with 8 N chromic acid solution. After the usual workup the residue is dissolved in methanol containing sodium hydroxide (0.2 g) and heated under reflux for 1 hr to remove any deuterium introduced at C-5 or C-7. (For workup, see section II-B). 

A solution of 11.2 g of potassium permanganate in 100 ml of warm water was added drop-wise to a well stirred solution of 10 g of 2-(4-chlorophenyl)-3-methyl-4-metathiazanone in 50 ml of glacial acetic acid. The temperature was kept below 30°C with external cooling. An aqueous sodium bisulfite solution was then added to remove the manganese dioxide. The thick whitish oil which separated was taken up in chloroform and the extract was washed with water. Removal of the chloroform by distillation in vacuo yielded an oily residue which solidified. The solid was recrystallized from isopropyl alcohol to give 5 g of the product, 2-(4-chlorophenyl)-3-methyl-4-metathiazanone-1,1-dioxide, MP 116.2° to 118.6°C (corr.). 

A mixture containing 8 g (0.06 mol) of N-methyl-3-chloro-piperidine and 13.6 g (0.06 mol) of benzilic acid in 50 cc of anhydrous isopropyl alcohol was refluxed for 3 days the isopropyl alcohol was removed by distillation in vacuo, the residue treated with dilute aqueous hydrochloric acid and the aqueous acid mixture extracted repeatedly with ether. The aqueous phase was separated, made strongly alkaline with 20% aqueous sodium hydroxide and extracted with ether. The ether extracts were dried with potassium carbonate and distilled the product was collected at 175° to 176°C (0.03 mm), yield 11.5 g (59%). The ester base thus prepared was then dissolved in 75 cc of isopropyl alcohol and 3.4 g (0.037 mol) methyl bromide added. The reaction mixture was allowed to stand at 30°C for 2 days and the product isolated by filtration, yield, 13 g (87%), MP 228° to 229°C dec. 

N-ethyl-3-chloropiperidine was prepared according to the method of Fuson and Zirkle described in Volume 70, J. Am. them. Soc., p 2760. 12.0 g (0.0B1 mol) of N-ethyl-3-chloropiperidine was mixed with 1B.6 g (0.0B1 mol) of benzilic acid and 80 cc of anhydrous isopropyl alcohol as a solvent. The mixture was refluxed for 72 hours. The solution was then filtered and concentrated at 30 mm of mercury. The concentrate was dissolved in water, acidified with hydrochloric acid and extracted with ether to remove the unreacted benzilic acid. 

This residue is dissolved in isopropyl alcohol and 1 gram N-bis-chloroethyl-aniline is added to it. The mixture is refluxed for 3 hours. The solvent is removed at a reduced pressure, the residue is treated with 50% potassium carbonate, and extracted with ether. By treating with ethereal hydrochloric acid, 2-N -m-chlorophenylpiperazino-propyl-s-triazole-[4,3-al-pyridine-3-one hydrochloride is precipitated MP 223°C. 

An unusual reaction is used to form a KRe 4 HjO. The reduction of potassium perrhenate in en-H20 solutions by potassium metal yields a white solid containing the Rh ion mixed with KOH. Extraction with isopropyl alcohol gives a colloidal brown liquid containing a mixture of KOH, isopropyl alcohol and the rhenidc. Fractional extraction of the liquid gives a gray solid that contains 5.5-60% KRe 4 HjO... 

Synthesis of Derivatizing Reagent III. We placed 50 mL of methanol, which had been previously dried over 4-S molecular sieves, in a 100-mL round-bottom flask and added 6.0 g of 2-hydroxynicotinic acid and 3 mL of boron trifluoride etherate. The solution was heated to reflux for 24 h and the solvent was removed under reduced pressure. The residue was dissolved in 50 mL of 0.1-ff sodium hydroxide and extracted with 60 mL of chloroform. The chloroform extract was concentrated under reduced pressure and the residue crystallized from isopropyl alcohol. The yield of 3-carbomethoxy-2(lH)pyridone was 5.0 g mp 152.5-154°C NMR (CDCI3) 6 3.85 (s, 3, -CH3), 6.34 (t, 1,... 

Reflux extraction of additives and wax from polyolefins was reported [116]. Subsequently, the additives were adsorbed onto an adsorbent (Florisil) and the wax was removed from the extract before chromatography. Boiling extractions of SBR are described in ASTM D 1416-89 1 g of rubber is extracted by boiling in two 100 mL portions of 75/25 vol% isopropyl alcohol/toluene. Reflux heating with strong solvents, such as THF, dichloromethane or chloroform has been reported [117]. Reflux extraction has also been used for the 3 h extraction of caprolactam and oligomers from PA6 in boiling methanol. 

A procedure that has been widely used for spray residues is the separation of the residue from the sample by extraction with an organic solvent, usually benzene. After most of the solvent has been removed, the residue is treated with sodium and isopropyl alcohol and the chloride ion is estimated by standard methods. Carter 10) has determined in this manner DDT residues on a number of crops, and he has recommended the adoption by the Association of Official Agricultural Chemists of the method as a tentative one for DDT 11). Koblitsky and Chisholm 42) have determined DDT in soil samples by the sodium-isopropyl alcohol procedure after removing the DDT by extraction with an azeotropic mixture of two volumes of benzene and one volume of isopropyl alcohol. 

Colorimetric methods (3, 6-10), some of which are specific, have been developed for the determination of DDT in small amounts. For benzene hexachloride (hexachloro-cyclohexane), chlordan, and toxaphene, however, specific analytical methods have not been developed, and their residues have been evaluated by the determination of organically bound chlorine. The procedure comprises extraction of the insecticide residue from the sample with benzene or other suitable organic solvent, evaporation of the solvent, treatment of the residue with isopropyl alcohol and metallic sodium, and finally determination by standard methods of the amount of chloride ion formed. 

All efforts of trying to extract the sodium salt into an organic solvent were unsuccessful, and, thus, a salting out procedure using the common ion effect was used. The product at this stage is in the aqueous phase and addition of 15 g of sodium chloride /100 mL of the reaction mixture, completely precipitates all the coupled sodium salt which is filtered. The filtered crude product is dewatered by washing with isopropyl alcohol or drying under vacuum. The mother liquors... 

Aminopyrazole may also be obtained by hydrolysis of 3-imino-l-(/>-tolylsulfonyl)pyrazolidine with aqueous alkali. In this case the pyrazolidine (239 g., 1.00 mole) is added to a solution of 40 g. (1.0 mole) of sodium hydroxide in 250 ml. of water at 75°, the resulting solution is stirred briefly, and the water is removed at reduced pressure. 3(5)-Aminopyrazole is separated from the sodium />-toluenesulfinate by several extractions with isopropyl alcohol. 

In the first experiment the contaminated extracts were obtained and then they were thermally treated by plasma. The analytical results showed that the best solvents for extraction of oil - PCB s were isooctane, cyclohexane, isopropyl alcohol and their mixture. We have found the average extraction efficiency 95%. The best result 96.2% of the extraction efficiency we obtained for the mixture of isooctane and isopropyl alcohol in the ratio 1 1. 

Simethicone is an antigas ingredient in many liquid and solid pharmaceutical preparations, and FTIR is used in quality assurance laboratories to determine whether its concentration is at the specified level. A sample of the product is dispersed in an HC1 solution and the simethicone extracted from this solution with toluene. The toluene solutions are then run on the FTIR using a liquid sampling cell. For the quantitative analysis, a simethicone absorption band that is free from interference from the toluene absorption bands is used in a manner similar to that of the isopropyl alcohol band in Experiment 26. 

Two studies compared sonication with Soxhlet extraction with pentane [13], acetone/hexane [13] and hexane/ispropyl alcohol (70 30) [5], The first two Soxhlet extraction solvents yielded lower recoveries than sonication, but the most polar solvent hexane/isopropyl alcohol gave recoveries and relative standard deviations for NP and NPE0i i9 comparable with sonication with hexane/acetone [5],... 

Because ethyl alcohol forms an azeotrope with water that is a constant boiling mixture, i.e. both the ethyl alcohol and the water, in a ratio of 95/5, boil together at a temperature different than either separately. Other examples in this chapter are the ternary azeotrope, ethyl alcohol - water -benzene and DIPE - isopropyl alcohol - water. An azeotrope mentioned earlier is MEK - water - toluene rafFmate used for toluene extraction. 

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