Methylamine 25% aqueous solution

Aminomethanamidine hydrochloride. See Guanidine hydrochloride Aminomethane. See Methylamine, aqueous solutions Methylamine 1-Amino-2-methoxybenzene. See o-Anisidine 1-Amino-4-methoxybenzene. See p-Anisidine... [Pg.228]

Carbethoxy malaoxon. See Malaoxon Carbethoxy malathion. See Malathion Carbethoxymethyl diethyl phosphonate. See Triethyl phosphonoacetate Carbethoxymethyl ethyl phthalate. See Ethyl phthalyl ethyl glycolate p-Carbethoxyphenol. See Ethylparaben 3-Carbethoxypyridine. See Ethyl nicotinate Carbinamine. See Methylamine, aqueous solutions Methylamine Carbinol. See Methyl alcohol Carbinoxamide maleate. See Chloropheniramine maleate Carbital 35] Carbital 50] Carbital 75] Carbital 90. See Calcium carbonate Carbitol Carbitol . See Ethoxydiglycol Carbitol acetate Carbitol Acetate. See Ethoxydiglycol acetate... [Pg.753]

Metham potassium. See Potassium N-methyldithiocarbamate Metham sodium. See Metam-sodium Methanal. See Formaldehyde Methanamide. See Formamide Methanamine. See Methylamine, aqueous solutions Methylamine Methanamine, N-methyl-. See Dimethylamine Methanamine, N-methyl-, compd. with borane (1 1). See Dimethylamine borane Methanamine, N-methyl-N-nitroso-. See N-Nitrosodimethylamine Methanamine, N-methyl-, polymer with (chloromethyl) oxirane. See Dimethylamine/epichlorohydrin copolymer Methanaminium, 1-carboxy-N,N,N-trimethyl-, chloride. See Betaine hydrochloride Methanaminium, N-(4-((2-chlorophenyl) (4-(dimethylamino) phenyl) methylene)-2,5-cyclohexadien-1-ylidene)-N-methyl-, chloride. See Basic blue 1... [Pg.2548]

Regulatory CERCLA hazardous substance Manuf./Distrib. Air Prods. http //www. air products, com Al d ri c h http //www.sigma-aldrich.com, Celanese Mexico http //www.celanese.com.mx, Chinook Group DuPont http //www.dupont.com MG Ind. http //www.mgindustries.com, Matheson Gas Prods. Penta Mfg. http //www.pentamfg.com. Spectrum Quality Prods. http //www.spectrumchemical.com See also Methylamine, aqueous solutions... [Pg.2580]

Methylamine, anhydrous. See Methylamine Methylamine, aqueous solutions CAS 74-89-5 EINECS/ELINCS 200-820-0 UN 1235... [Pg.2580]

MMA. See Methylamine, aqueous solutions Methylamine Dimethyl anthranilate Methyl methacrylate... [Pg.2724]

Monomethylacetamide. See N-Methylacetamide Monomethyl adipate. See Methyl adipate Monomethylamine. See Methylamine, aqueous solutions Methylamine Monomethyl aminoethanol. SeeN-Methylethanolamine... [Pg.2735]

Lignin sulfonate Methylamine, aqueous solutions 1-Naphthol 1,4-Naphthoquinone o-Nitrobenzaldehyde... [Pg.5133]

Aluminum acetylacetonate 1,2-Butylene carbonate Chromic acetylacetonate Cobalt acetate (ous) Cobalt acetylacetonate Copper nitrate (ic) Ethylene carbonate Ferric acetylacetonate Hexyloxypropylamine Isodecyloxypropylamine N-lsodecyloxypropyl 1-1,3-diaminopropane Magnesium acetylacetonate Manganese acetylacetonate Methylamine Methylamine, aqueous solutions... [Pg.5334]

Methylamine Methylamine, aqueous solutions Octylphenol Propyl mercaptan 1,2,4,5-Tetrachlorobenzene Urethane... [Pg.5399]

Ethyl chloride Ethylene thiourea Ethyl mercaptan Fluorobenzene Hexachlorocyclopentadiene Isobutyronitrile Isopropylamine 2-Mercaptoethanol Methylamine Methylamine, aqueous solutions Methylene bromide 2-Nitropropane Phosphorus pentasulfide n-Propyl bromide Trichloroethylene... [Pg.5400]

Methylamine Methylamine, aqueous solutions 4,4 -Methylenebis (3-chloro-2,6-diethylaniline) Methylene bromide Methyl formate... [Pg.5403]

Meroxapol 174 Meroxapol 251 Meroxapol 252 Meroxapol 254 Meroxapol 258 Meroxapol 311 Methanesulfonyl chloride Methoxymethyl isocyanate p-Methoxyphenylacetic acid Methyl acetate Methyl acetoacetate 4 -Methyl acetophenone Methylamine Methylamine, aqueous solutions Methyl anthranilate Methyl carbamate Methyl chloride 1,2-Methylenedioxybenzene N-Methylethanolamine N-Methylformamide Methyl 2-furoate 4-Methylpentanoic acid 1-Methylpiperidine 2-Methylpiperidine 3-Methylpiperidine 4-Methylpiperidine 1-Methyl-2-piperidineethanol Methyl pivalate 4-(Methylsulfonyl) acetophenone 4-(Methylthio) acetophenone... [Pg.5407]

Dimethyl acetamide Ethylene dichloride Isopropyl ether Mesityl oxide Methylamine Methylamine, aqueous solutions Phenoxyethanol Potassium hydroxide Propylene glycol phenyl ether 1,1,2,2-Tetrachloroethane... [Pg.5502]

Diammonium EDTA Diethylhydroxylamine Dimethylol urea Methylamine Methylamine, aqueous solutions... [Pg.5521]

Hydrazine Lanthanum Lithium Lithium nitrate Methylamine Methylamine, aqueous solutions Nitrocellulose Nitroglycerin 1-Nitropropane 2-Nitropropane propellant, rocket fuels Tetranitromethane propellant, rocket liquid Ammonium thiocyanate Hydrofluoric acid propellant, rocket smokeless Ammonium perchlorate propellant, rocket solid Beryllium... [Pg.5579]

Methylamine Methylamine, aqueous solutions Naphthalene Potassium alum anhydrous Potassium bisulfite... [Pg.5805]

Preheat a water bath on the stove (or wherever) to about 80C and place the stainless steel mixing bowl in it. Once the temperature of the solution hits about 65C, take the bowl out and set aside while stirring all the while. This is where it rearranges, and the reaction is exothermic enough to sustain it s temperature nicely. If you find the temperature climbing past 80C, immerse the bowl into some cold waiter briefly. After about 15 minutes the temperature will start to fall, at which point you should transfer the whole mess to the distilling flask. Before you continue you need to choose whether you want to make the hydrochloride salt or the aqueous solution of Methylamine, though. [Pg.263]

For the aqueous solution Place 16mL of cool distilled water into your bubbler setup. The "expected, not theoretical, yield of Methylamine from this amount of reactants is 7 grams. I have used a plastic aquarium aerator tube as the bubbler with excellent results. Sure beats using an inverted funnel. [Pg.264]

Let us define the respective basicity by — AG in the gas phase and — AG" in aqueous solution. For discussions concerning the relative strength in basicity of a series of methyl-amines, only the relative magnitudes of these quantities are needed. Thus the free energy changes associated with the protonation of the methylamines relative to those of ammonia are defined as... [Pg.429]

Free energy changes of methylamines m aqueous solution upon protonation refeiTed to... [Pg.429]

Using maleic aldehyde, acetonedicarboxylic acid and methylamine hydrochloride in aqueous solution, in presence of sodium acetate, Iheobrazhenskii, Rubtsov, Dankova and Pavlov have prepared troperume. [Pg.80]

First,0.27 mol of a-chloro-3, 4 -dihydroxyacetophenone are dissolved in 200 ml methanol with warming. Next, 100 ml of a 40% aqueous solution of methylamine is slowly added and the mixture stirred at 50°C to 55°C for 2 hours. The reaction mixture is then stirred an additional 24 hours at room temperature. [Pg.523]

Methylchloramine can be prepared by adding an aqueous solution of sodium hypochlorite to an aqueous solution of methylamine in accordance with the process described by W.S. Metcalf, J. Chem. Soc. 1942,148. [Pg.957]

Methylamine (CH3NH2) is a gas at room temperature and very soluble in water. An aqueous solution of methylamine has Kb = 4.2 X 10-4. How many liters of methylamine at 27°C and a pressure of 1.2 atm should be bubbled into 0.750 Lofa solution that is 0.588 M in the methylammonium ion (CH3NH3+) so that a buffer of pH 9.80 is obtained Assume no volume changes after methylamine is bubbled into the solution and ignore the vapor pressure of water. [Pg.404]

In a 2-1. flask provided with a mechanical stirrer, separatory funnel, and thermometer, are placed 189 g. (2 moles) of chloro-acetic acid and 150 cc. of water. The flask is cooled in ice water, and a cold solution of 160 g. (4 moles) of sodium hydroxide in 500 cc. of water is added, with stirring, at such a rate that the temperature does not exceed 30° (Note 1). AfLer all the alkali has been added, the cooling bath is removed, and an aqueous solution (Note 2) containing 31 g. (1 mole) of methylamine is added slowly. The reaction is exothermic, and the temperature is kept below 50° by occasional immersion of the flask in ice water. After all the methylamine has been added, the solution is allowed to stand for two hours to complete the reaction. [Pg.56]

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