N-Amyl Mercaptan

Amyl Acetates, Mixed Isomers N-Amyl Alcohol 1-Amyl Alcohol Amyl Aldehyde Amyl Carbinol Amyl Chloride N-Amyl Chloride Alpha-N - Amylene Amyl Hydrosulfide N-Amyl Mercaptan N-Amyl MethylKetone N-Amyl Nitrate... [Pg.22]

N-Amyl Mercaptan N-Amyl Mercaptan N-Amyl Methyl Ketone N-Amyl Nitrate... [Pg.22]

Glutaraldehyde Solution Acetylacetone N-Amyl Mercaptan N-Amyl Alcohol Pentaerythritol 1-Pentene Amyl Acetate N-Amyl Alcohol Ethyl Butanol N-Amyl Chloride N-Amyl Methyl Ketone N - Amyltrochlorosilane Peracetic Acid Urea Peroxide Perchloric Acid Perchloric Acid... [Pg.74]

SYNS AMYL HYDROSULFIDE n-AMYL MERCAPTAN AMYL MERCAPTAN (DOT AMYL SULFHYDR-ATE AMYL THIOALCOHOL MERCAPTAN AMYLIQUE (FRENCH) PENTYL MERCAPTAN... [Pg.1076]

Sulfhydryl compounds are oxidized with ease to disulfides. It is necessary to employ mild oxidizing agents that do not attack the product. Oxidation of an alkaline solution of n-amyl mercaptan by iodine is described for -amyl disulfide (68%). A mixed disulfide, ethyl /-butyl disulfide, is obtained in 63% yield by treatment of an equimolecular mixture of ethyl and /-butyl mercaptans with iodine in ethanol. Hydrogen peroxide is probably the best reagent for the oxidation. " Halo and amino groups in the molecule are unaffected. Benzoyl disulfide, CtHsCOSSCOCjH, is conveniently prepared by the iodine oxidation of the potassium salt of thiobenzoic acid, C4H5COSK. ... [Pg.850]

Iodine (60.3 g., 0.48 gram atom) is added in small portions over a period of 20 minutes to a solution of 52 g. (0.50 mole) of n-amyl mercaptan and 22 g. (0.55 mole) of sodium hydroxide in 125 ml. of water. The mixture is stirred until all the iodine is dissolved and then is extracted with 200 ml. of benzene. The resulting benzene solution is washed three times with water, dried over sodium sulfate, and distilled to give 36 g. (70%) of di-n-amyl disulfide, b.p. 101-103°/2 mm., 1.4868. [Pg.107]

AMYL MERCAPTAN or n-AMYL MERCAPTAN (110-66-7) Forms explosive mixture with air (flash point 65°F/18°C). Ignites on contact with concentrated nitric acid. Contact with water, steam, or acids produces toxic and flammable vapors. Incompatible with oxidizers, reducing agents, alkali metals, calcium hypochlorite. [Pg.109]

Pentanethiol (n-amyl mercaptan) [110-66-7] Benzenethiol (phenyl mercaptan) [108-98-5] 46 (rats) 2,000/4 h (rats) (LClo) 33/4 h (rats)... [Pg.873]

CAS 110-66-7 EINECS/ELINCS 203-789-1 UN 1111 (DOT) 1228 (DOT) 3071 (DOT) Synonyms Amyl hydrosulfide Amyl mercaptan n-Amyl mercaptan Amyl sulfhydrate Amyl thioalcohol... [Pg.3243]

N-Amyl Mercaptan N-Amyl Mercaptan N-Amyl Methyl Ketone N-Amyl Nitrate Iso-Amyl Nitrite Iso-Amyl Nitrite N-Amyl Mercaptan N-Amyl Mercaptan N-Amyltrichlorosilane Ethyl Ether... [Pg.129]