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Methyl carbitol

Methylbutyl Nitrite 3-Methylbutyraldehyde Methyl Carbitol Methyl Cellosolve Methyl Chloride Methyl Chlorocarbonate Methyl Chloroform Methyl Chlorofonnate... [Pg.64]

Cellosolve Methyl Cellosolve Butyl Cellosolve Carbitol Methyl Carbitol Butyl Carbitol... [Pg.17]

Mobile liquids, pastes or flakeable solids. Relatively nonhygroscopic. Vary from water-insol to very water-sol compds more sol in cold than hot water. In general, sol in iromatic solvents (benzene, toluene, xylene), chlorinated solvents, acetone, ale, propylene or hexylene glycol, butyl cdlosolve, butyl carbitol, methyl ethyl ketone, cyclohexanone. Insol in ethylene glycol, kerosene, mineral oil. Low-looming properties. Stable to acids, alkalies, metallic ions. [Pg.1203]

Union Carbide Propyl Celloso v Butyl Cettosotve - Methyl CarMol Carbifot (low gravity) Propyl Carbitol Butyl Carbitol Methyl Prop ml... [Pg.839]

CAS 111-77-3 EINECS/ELINCS 203-906-6 Synonyms DEGME Diethylene glycol methyl ether Diethylene glycol monomethyl ether Ethanol, 2-(2-methoxyethoxy)- 2-(2-Methoxyethoxy) ethanol Methyl Carbitol Methyl digol Classification Aliphatic ether alcohol Empin cal C5H12O3 Formula CH3OCH2CH2OCH2CH2OH Properties Water-wh. liq. mild pleasant odor sol. in water, alcohols, glycerol, ether, acetone misc. with most org. soivs. m.w. 120.17 dens. 1.0211 (20/4 C) vapor pressure 0.2 mm Hg (20 C) m.p. -85 C b.p. 194 C flash pt. 93.3 C ref. index 1.4264(27 C)... [Pg.2558]

Methyl-4-carbethoxy-4-phenyl hexamethyleneimine. See Ethofumesate Methylcarbinol. See Alcohol Methyl Carbitol Methyl Carbitol . See Methoxydiglycol... [Pg.2602]

Butyne-l,4-diol Amyl Mercaptan 111-82-0 Methyl Carbitol Methyl Laurate... [Pg.3483]

The mono-methyl, ethyl and n-butyl ethers are inexpensive commercial products and are known as methyl carbitol, carbitol and butyl carbitol respectively. They are all completely miscible with water and are purified as already described for the cellosolves (10). The boiling points of the pure compounds are —... [Pg.171]

Place 0 -5 g. of 3 4 5 triiodobenzoyl chloride in a small test-tube, add 0 -25 ml. of the alcohol - ether and heat the mixture gently over a micro burner until the evolution of hydrogen chloride ceases (3-5 minutes). Pour the molten mass into 10 ml. of 20 per cent, alcohol to which crushed ice has been added. Some derivatives solidify instantly those which separate as oils change to solids in a few minutes without further manipulation. Recrystallise from rectified spirit (use 50 per cent, alcohol for esters of methyl and butyl carbitol ). [Pg.265]

The following melting points have been recorded —methyl cellosolve, 152° cellosolve, 128° wo-propyl cellosolve, 80° butyl cellosolve, 85° phenyl cellosolve, 145° benzyl cellosolve, 104° methyl carbitol. 82° ethyl carbitol, 76° . butyl carbitol, 54°. [Pg.265]

Methyl n-ptopyl carbinol (6) Cetyl alcohol (11) Ethyl celloBOlve (16) Butyl carbitol ... [Pg.269]

The monoalkyl ethers with R = CHj, CjHj and C4H, , known respectively as methyl ceUoaolve, ceUosolve and hutyl cellosolve, are of great commercial value, particularly as solvents, since they combine the properties of alcohols and ethers and are miscible with water. Equally important compounds are the carbitols (monoalkyl ethers of diethyleneglycol) prepared by the action of ethylene oxide upon the monoethers of ethylene glycol ... [Pg.444]

Thus with R = CHj, CjHj and C H, , the compounds are called methyl carhitoli carbitol and butyl carbitol respectively. None of these compounds can be conveniently prepared in the laboratory by elementary students they are, however, readily available commercially. The preparation of one glycol, pinacol or tetramethylene glycol from acetone, has already been described (Section 111,77). [Pg.444]

Actinide ions form complex ions with a large number of organic substances (12). Their extractabiUty by these substances varies from element to element and depends markedly on oxidation state. A number of important separation procedures are based on this property. Solvents that behave in this way are thbutyl phosphate, diethyl ether [60-29-7J, ketones such as diisopropyl ketone [565-80-5] or methyl isobutyl ketone [108-10-17, and several glycol ether type solvents such as diethyl CeUosolve [629-14-1] (ethylene glycol diethyl ether) or dibutyl Carbitol [112-73-2] (diethylene glycol dibutyl ether). [Pg.220]

Methyl carbitol, m73 4-Methylcatechol, d438 Methyl cellosolve, m71 Methyl cellosolve acetate, m75 Methyl chlorocarbonate, ml94 Methyl chloroform, t231... [Pg.263]

Methyl carbitol see diethylene glycol monomethyl ether. [Pg.266]

DIETHYLENE GLYCOL MONOMETHYL ETHER (METHYL CARBITOL) ... [Pg.74]

METHYL CARBITOL (see DIETHYLENE GLYCOL MONOMETHYL ETHER, p.71) METHYL CELLOXOLVE (see 2-METHOXYETHANOL, p.117) METHYL CELLOXOLVE ACETATE (2-METHOXYETHYLACETATE) Water <20 284... [Pg.123]

Methyl Carbitol solvent Sodium xylene sulfonate Sodium carbonate Pine oil Water... [Pg.66]

See other pages where Methyl carbitol is mentioned: [Pg.376]    [Pg.415]    [Pg.376]    [Pg.376]    [Pg.415]    [Pg.376]    [Pg.269]    [Pg.408]    [Pg.362]    [Pg.268]    [Pg.268]    [Pg.269]    [Pg.57]    [Pg.677]    [Pg.391]    [Pg.391]    [Pg.391]    [Pg.269]    [Pg.1170]    [Pg.187]   
See also in sourсe #XX -- [ Pg.171 , Pg.444 ]

See also in sourсe #XX -- [ Pg.171 , Pg.444 ]

See also in sourсe #XX -- [ Pg.171 , Pg.444 ]

See also in sourсe #XX -- [ Pg.171 , Pg.444 ]



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