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Odors acetic acid

The first members of the carboxylic acid series are colorless liquids with sharp or unpleasant odors. Acetic acid, which constitutes about 4% to 5% of vinegar, provides the characteristic odor and flavor. Butyric acid gives rancid butter its disagreeable odor, and the goat acids (caproic, caprylic, and capric in Table 10.1) smell like goats. 3-Methyl-2-hexenoic acid, produced by bacteria, is responsible for the offensive odor of human armpits. Table 10.3 lists some physical properties of selected carboxylic acids. [Pg.291]

METHOD 2 [89]--1M MDA or benzedrine and 1M benzaldehyde is dissolved in 95% ethanol (Everclear), stirred, the solvent removed by distillation then the oil vacuum distilled to give 95% yellow oil which is a Schiff base intermediate. 1M of this intermediate, plus 1M iodomethane, is sealed in a pipe bomb that s dumped in boiling water for 5 hours giving an orangy-red heavy oil. The oil is taken up in methanol, 1/8 its volume of dH20 is added and the solution refluxed for 30 minutes. Next, an equal volume of water is added and the whole solution boiled openly until no more odor of benzaldehyde is detected (smells like almond extract). The solution is acidified with acetic acid, washed with ether (discard ether), the MDMA or meth freebase liberated with NaOH and extracted with ether to afford a yield of 90% for meth and 65% for MDMA. That s not a bad conversion but what s with having to use benzaldehyde (a List chemical) Strike wonders if another aldehyde can substitute. [Pg.159]

Acetic acid has a sharp odor and the glacial acid has a fiery taste and will penetrate unbroken skin to make bUsters. Prolonged exposure to air containing 5—10 mg/m does not seem to be seriously harmful, but there are pronounced, undesirable effects from constant exposure to as high as 26 mg/m over a 10-day period (8). [Pg.70]

Care ought to be taken in handling acetic acid to avoid spillage or otherwise breathing vapors. Wash any exposed areas with large amounts of water. Once the odor of acetic acid vapors is noticeable, the area should be abandoned immediately. The U.S. threshold limit value for acetic acid is 10 ppm (25 mg/m ). Similar values prevail in Germany (75). [Pg.70]

Acetamide [60-35-5] C2H NO, mol wt 59.07, is a white, odorless, hygroscopic soHd derived from acetic acid and ammonia. The stable crystalline habit is trigonal the metastable is orthorhombic. The melt is a solvent for organic substances it is used ia electrochemistry and organic synthesis. Pure acetamide has a bitter taste. Unknown impurities, possibly derived from acetonitrile, cause its mousy odor (1). It is found ia coal mine waste dumps (2). [Pg.73]

Acetic anhydtide [108-24-7] (CH2C0)20, is a mobile, colorless liquid that has an acrid odor and is a more pierciag lacrimator than acetic acid [64-19-7]. It is the largest commercially produced carboxyUc acid anhydride U.S. production capacity is over 900,000 t yearly. Its chief iadustrial appHcation is for acetylation reactions it is also used ia many other appHcations ia organic synthesis, and it has some utility as a solvent ia chemical analysis. [Pg.75]

Physical Properties. Trifluoroacetic acid [76-05-1], CF COOH, is a colorless Hquid with a sharp odor resembling that of acetic acid. Its... [Pg.307]

Ranitidine. Ranitidine hydrochloride [66357-59-3] (Zantac) is a white to pale yellow granular substance. It is freely soluble in water and acetic acid, soluble in methanol, sparingly soluble in ethanol, and practically insoluble in chloroform. It has a slightly bitter taste and a sulfur-fike odor. It may be made by the method described in Reference 5. [Pg.199]

Castor Oil. Castor oil [8001-79-4] (qv) is the fixed oil from the seeds of Picinus communis Linne. Pale yellowish or almost colorless, it is a transparent viscid Hquid with a faint, mild odor and a bland taste followed by a slightly acrid and usually nauseating taste. Its specific gravity is between 0.945 and 0.965. Castor oil is soluble in alcohol, and miscible with anhydrous alcohol, glacial acetic acid, chloroform, and diethyl ether. It consists chiefly of the glycerides of ricinoleic acid [141 -22-0], and isoricinoleic acid [73891-08-4], found in the small intestine. The seed contains a highly... [Pg.201]

Nickel acetate tetrahydrate [6018-89-9] Ni(C2H202) 4H2O, is a green powder which has an acetic acid odor, density 1.74 g/cm. When heated, it loses its water of crystallization and then decomposes to form nickel oxide. Nickel acetate is used as a catalyst intermediate, as an intermediate in the formation of other nickel compounds, as a dye mordant, as a sealer for anodized aluminum, and in nickel electroplating (59). [Pg.13]

Physical Properties. Sulfuryl chloride [7791-25-5] SO2CI2, is a colorless to light yellow Hquid with a pungent odor. Physical and thermodynamic properties are Hsted ia Table 7. Sulfuryl chloride dissolves sulfur dioxide, bromine, iodine, and ferric chloride. Various quaternary alkyl ammonium salts dissolve ia sulfuryl chloride to produce highly conductive solutions. Sulfuryl chloride is miscible with acetic acid and ether but not with hexane (193,194). [Pg.142]

The Prins reaction with formaldehyde, acetic acid, acetic anhydride, and camphene gives the useful alcohol, 8-acetoxymethyl camphene, which has a patchouli-like odor (83). Oxidation of the alcohol to the corresponding aldehyde also gives a useful iatermediate compound, which is used to synthesize the sandalwood compound dihydo- P-santalol. [Pg.416]

Uses ndReactions. Linalool can be estetified to linalyl acetate by reaction with acetic anhydride. Linalyl acetate [115-95-7] has a floral-fmity odor, reminiscent of bergamot and lavender. The price of the acetate in 1995 was 14.30/kg (45). Linalool is subject to dehydration and to isomerization to nerol and geraniol during the esterification. However, if the acetic acid formed during the esterification is removed in a distillation column, the isomerization can be minimized and good yields of the acetate obtained (130). [Pg.421]

Bismuth subgaHate [12552-60-2] (basic bismuth gaHate), Dermatol, is a bright yellow powder that can be prepared by the interaction of bismuth nitrate and gaUic acid in an acetic acid medium. It has been employed as a dusting powder in some skin disorders and as an ingredient of suppositories for the treatment of hemorrhoids (183,185). It has been taken orally for many years by colostomy patients in order to control fecal odors, but the dmg may cause serious neurological problems (186). [Pg.135]

Chlorotoluene [95-49-8] (l-chloto-2-methylben2ene, OCT) is a mobile, colorless Hquid with a penetrating odor similar to chlorobenzene. It is miscible ia all proportions with many organic Hquids such as aUphatic and aromatic hydrocarbons, chlorinated solvents, lower alcohols, ketones, glacial acetic acid, and di- -butylamine it is iasoluble ia water, ethylene and diethylene glycols, and triethanolamine. [Pg.52]

Cyclohexanol [108-93-0] is a colorless, viscous liquid with a camphoraceous odor. It is used chiefly as a chemical iatermediate, a stabilizer, and a homogenizer for various soap detergent emulsions, and as a solvent for lacquers and varnishes. Cyclohexanol was first prepared by the treatment of 4-iodocyclohexanol with ziac dust ia glacial acetic acid, and later by the catalytic hydrogenation of phenol at elevated temperatures and pressures. [Pg.425]

Paint and varnish manufacturing Resin manufacturing closed reaction vessel Varnish cooldng-open or closed vessels Solvent thinning Acrolein, other aldehydes and fatty acids (odors), phthalic anhydride (sublimed) Ketones, fatty acids, formic acids, acetic acid, glycerine, acrolein, other aldehydes, phenols and terpenes from tall oils, hydrogen sulfide, alkyl sulfide, butyl mercaptan, and thiofen (odors) Olefins, branched-chain aromatics and ketones (odors), solvents Exhaust systems with scrubbers and fume burners Exhaust system with scrubbers and fume burners close-fitting hoods required for open kettles Exhaust system with fume burners... [Pg.2177]

Problem A 2 ft diameter packed scrubber, removing acetic acid from process offgas had excessive acetic acid emissions causing unacceptable losses and odors. [Pg.310]

In humid weather the solid often deliquesces, and this necessitates drying in a desiccator. The material retains acetic acid very tenaciously, and drying should be continued until the odor of the solvent no longer can be noticed. [Pg.2]

Observable Characteristics - Physical State (as normally shipped) Solid Color Pink Odor Slight acetic acid odor vinegar-like. [Pg.87]

Chemical Designations - Synonyms Lead (IV) acetate Chemical Formula Pb(C2H302)4-CH3COOH. Observable Characteristics - Physical State (as shipped) Crystals wet with glacial acetic acid Color Faintly pink Odor Like acetic acid or vinegar. [Pg.234]

Many carboxylic acids were first isolated from natural sources and were given names based on their origin. Fonnic acid (Latin formica, meaning ant ) was obtained by distilling ants. Since ancient times acetic acid (Latin acetum, for vinegar ) has been known to be present in wine that has turned sour. Butyric acid (Latin butyrum, meaning butter ) contributes to the odor of both rancid butter and ginkgo benies, and lactic acid (Latin lac, for milk ) has been isolated from sour milk. [Pg.806]

Acetaldehyde is a colorless liquid with a pungent odor. It is a reactive compound with no direct use except for the synthesis of other compounds. For example, it is oxidized to acetic acid and acetic anhydride. It is a reactant in the production of 2-ethylhexanol for the synthesis of plasticizers and also in the production of pentaerithritol, a polyhydric compound used in alkyd resins. [Pg.198]

Cydopantene-oxo-ozonidas. A monomer, C5Ha03, was prepd (Ref 2) by the ozonization of cyclo pentene dissolved in CC14. It is a yel, volatile liq with a penetrating odor sol in chlf, ethyl acetate and acetic acid is decompd explosively by coned sulfuric acid explds on heating... [Pg.472]


See other pages where Odors acetic acid is mentioned: [Pg.62]    [Pg.62]    [Pg.271]    [Pg.806]    [Pg.48]    [Pg.64]    [Pg.81]    [Pg.98]    [Pg.444]    [Pg.277]    [Pg.314]    [Pg.332]    [Pg.58]    [Pg.286]    [Pg.409]    [Pg.409]    [Pg.463]    [Pg.392]    [Pg.78]    [Pg.238]    [Pg.5]    [Pg.6]    [Pg.81]    [Pg.82]    [Pg.751]    [Pg.727]   
See also in sourсe #XX -- [ Pg.404 ]




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