Amyl Sulfide

Aminonaphtholsulfonic acids, coupling to form azo dyes, 16, i6 Aminopbenol, 15, 39 Amiuopiperole, 16, 6 P-Amlnopropionic acid, 16, 1 4-Aminoveraxroie, 16, 4-Ammonium dichromate, 16, 74 Ammonium thiocyanate, 16, 74 Ammonium vanadate, 13, no -Amyl alcohol, 13,17 feft.-Amyl alcohol, 13, 68 -Amyl benzene, 10, i -Amyl borate, 13,17 -Amyl bromide, 16, 41 ijo-Amyl iodide, 13, 62 -Amyl iodide, 13, 62 -Amylmagnesium bromide, 16, 4r ire-Amyl nitrite, 16, 8 -Amyl phosphate, 16,10 sec.-Amyl sulfide, 16, 73 Aniline, 11, 62 IS, 96 14, 24 16, 59 Aniline hydrochloride, 13, 46 Aotline-o-SULEONIC acid, 16, 55 Anisalacetone, 10, IIS Anthracene, 16, 74 Anthranilic add, 12, 76 Anthraquinone, 14, 4 16, 74 Apparatus... 

Aqueous sodium thiosulfate solutions ate neutral. Under neutral or slightly acidic conditions, decomposition produces sulfite and sulfur. In the presence of air, alkaline solutions decompose to sulfate and sulfide. Dilute solutions can be stabilized by small amounts of sodium sulfite, sodium carbonate, or caustic, and by storage at low temperatures away from air and light. Oxidation is inhibited by Hgl2 (10 Ppm) amyl alcohol (1%), chloroform (0.1%), borax (0.05%), or sodium benzoate (0.1%). 

Diazoaminobenzene has been prepared by the action of sodium nitrite on aniline sulfate by the action of sodium nitrite on aniline hydrochloride by the action of sodium nitrite and sodium acetate on aniline hydrochloride by the action of ammonium nitrate and hydrogen sulfide on aniline hydrochloride in the presence of iron and by the action of amyl nitrite on aniline. ... 

Nitro-filter cloths are composed of cellulose nitrate, which is an ester of cellulose. Any chemical compound that will saponify the ester will destroy the cloth. Caustic soda or potash in strengths of 2% at 70° C or over alkali sulfides, polysulfides and sulfohydrates or mixtures of ethyl alcohol and ether, ethyl, amyl and butyl acetates, pyridine, ferrous sulfates, and other reducing agents are detrimental to the cloth. 

Ammonium sulfide, 3, n Ammonium thiocyanate, 7, 48 Ammonolysis, 4, 3 7, 16 o-Amyl alcohol, 1, 4, 10 Amyl alcohol, active, 7, 77 mo-Amyl Bromide, 1,1, 2, 4, 10 w-Amyl Methyl Ketone, 7, do -Amyl propiolic acid, 7, 62 Analysis of Benzoylhydroperoxide, 8,32 Analysis of Benzoylperoxide, 8, 31 Anhydro-o-Hydroxymercoribenzoic Acid, 7, 3... 

A number of workers have described methods for the determination of mercury in which the mercury is first reduced to the element or collected as the sulfide on a cadmium sulfide pad. It is then volatilized into a chamber for measurement. These techniques are extremely sensitive. Thillez108) recently described a procedure for urinary mercury in which the mercury is collected on platinum and then volatilized into an air stream. Rathje109) treated 2 ml of urine with 5 ml of nitric acid for 3 min, diluted to 50 ml, and added stannuous chloride to reduce the mercury to the element. A drop of Antifoam 60 was added and nitrogen was blown through the solution to carry the mercury vapor into a quartz end cell where it is measured. Six nanograms of mercury can be detected. Willis 93) employed more conventional methods to determine 0.04 ppm of mercury in urine by extracting it with APDC into methyl-n-amyl ketone. Berman n°) extracted mercury with APDC into MIBK to determine 0.01 ppm. 

Thisis due to hydrogen sulfide gas being generated in the stomach.lt is a bit unpleasant, but not dangerous. If you feel yourself developing the symptoms of cyanide poisoning, break an ampoule of amyl nitrite and inhale its contents. Seek medical attention. The foregoing does not mean that with the antidotes you can inhale fumes with impunity, only that you prob-... 

The previously discussed reductions by yeast of isovaleraldehyde to isoamyl alcohol, of p-xyloquinone to p-xylohydroquinone and of sodium thiosulfate to hydrogen sulfide have also been accomplished with Bacterium coli and Bacterium lactis aerogenes. Phytochemical reduction of d,l-valeraldehyde (methylethylacetaldehyde) with Termobacterium mobile Lindner Pseudomonas Lindneri) takes a practically quantitative course and yields an amyl alcohol containing 17 % excess of the dextrorotatory component. Cahill achieved especially favorable results by the reduction of isovaleraldehyde with growing bacteria instead of with their mass cultures. 

Compound Name Ammonium Oxalate Ammonium Oxalate Ammonium Pentaborate Ammonium Pentaborate Zinc Ammonium Chloride Ammonium Perchlorate Ammonium Persulfate Ammonium Persulfate Ammonium Phosphate Ammonium Phosphate Ammonium Thiocyanate Ammonium Thiocyanate Ammonium Silicofluoride Ammonium Stearate Ammonium Sulfamate Ammonium Sulfate Ammonium Sulfide Ammonium Sulfide Ammonium Sulfide Ammonium Sulfite Ammonium Thiocyanate Ammonium Thiocyanate Ammonium Tartrate Ammonium Thiocyanate Ammonium Thiosulfate Zinc Ammonium Chloride Phosphorus, Red Ammonium Sulfamate Amyl Acetate Amyl Acetate N-Amyl Alcohol N-Amyl Alcohol Valeraldehyde Hexanol... 

---