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N-Amyl thiocyanate

A mixture of 340 ml. of ethanol and 147 g. (1.52 moles) of potassium thiocyanate is heated to reflux, and 157 g. (1.04 moles) of n-amyl bromide is added dropwise. Reflux is continued for 2 hours after completion of the addition of the bromide. Most of the ethanol is removed by distillation, and the residue is diluted with water and extracted with ether. The combined ethereal extracts are dried over calcium chloride, and the ether is removed by distillation. Fractional distillation of the residue at 16 mm. pressure gives an 85% yield of n-amyl thiocyanate, b.p. 90-91°. [Pg.29]

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... [Pg.130]

I-A1ON0-2-NAPHIH0L-4-SULE0NIC acid, 11, 72 16, 91 17, 91 Aminonaphtholsulfonic acids, coupling to form azo dyes, 16,16 p-Aminophenol, 16, 39 Aminopiperole, 16, 6 /3-Ahinopropionic acid, 16, 1 4-Aminoveratrole, 16, 4 Ammonium dichromate, 16, 74 Ammonium formate, 17, 77 Ammonium thiocyanate, 16, 74 Ammonium vanadate, 13, 1 to w-Amyl alcohol, IS, 17 hri.-Amyl alcohol, 13, 68 -Amylbenzene, 10, 4 -Amyl borate, 13, 17 -Amyl bromide, 16, 41 iso-Amyl iodide, 13, 62 n-Amyl iodide, 13, 62 n-Amybnagnesium bromide, 16, 41... [Pg.90]

The theory of melting continues to be the subject of recent publications, including consideration of vacancy concentrations near the melting point [8,9], lattice vibrations and expansions [8,10—12], Meanwhile, the phenomenon also continues to be the subject of experimental investigations Coker et al. [13], from studies of the fusion of tetra-n-amyl ammonium thiocyanate, identify the greatest structural change as that which... [Pg.2]

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... [Pg.22]

One of the first observations of such stepwise, separate phase transitions of the paraffinic part of an amphiphilic molecule was made on tetra-n-amyl ammonium thiocyanate At 315 K the crystals undergo a major first-order transition [AS = 71 J/(K mol) with a 4.8 % volume change]. The final transition to the isotropic, molten salt at 323 K is entropically smaller [AS. = 59 J/(K mol) with a n gible volume change]. Since typical alkali thiocyanate entropies of fusion are 30-40 J/(K mol) it is reasonable to assume that the high-temperature crystal state is that of a condis crystals with considerable conformational freedom. [Pg.80]

Coker TG, Wunderlich B, Janz GJ (1969) Melting mechanisms of ionic salts Tetra-n-amyl-ammonhun thiocyanate. Trans. Farad. Soc. 65 3361... [Pg.118]

Alkyl thiocyanates, R—S—C=N, of lower carbon numbers are highly toxic. These compounds liberate HCN as a result of metabolic processes and can cause death (Manahan 1989). Methyl thiocyanate [556-64-9] is highly toxic, with an intravenous LD50 value of 18 mg/kg in mice (NIOSH 1986). Ethyl thiocyanate [542-90-5], allyl thiocyanate [764-49-8], butyl thiocyanate [628-83-1], and amyl thiocyanate [32446-40-5] are all toxic compounds with an LD50 (subcutaneous) value of less than 100 mg/kg. The phenyl ester [5285-87-0] exhibits greater toxicity (intravenous LD50 value in mice 6.7 mg/kg) than that of the aliphatic esters of thiocyanic acid. [Pg.873]

Compound Name 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... [Pg.129]

Ammonium Standard Solution, 849 Ammonium Sulfanilate TS, 850 Ammonium Sulfate, 28 Ammonium Sulfide TS, 850 Ammonium Thiocyanate, 0.1 N, 856 Ammonium Thiocyanate TS, 850 Amyl Acetate, 510 1-Amyl Alcohol, 454, (S3)66 Amylase, 130, (S3)18 a-Amylase, 132, 786 P-Amylase, 132, 786 Amyl Butyrate, 454, 510, (S3)66 Amyl Caprylate, 454 Amylcinnamaldehyde, 454 a-Amylcinnamaldehyde, 454, 605,... [Pg.118]

The 10-mlnute Co82 produced by the Ni82(n,p) reaction has been extracted as the thiocyanate into an organic layer of amyl alcohol-ethyl ether (l l) from a weak hydrochloric acid solution saturated with ammonium thiocyanate and then back-extracted with 6 N ammonia solution (156,208). The 5-2-minute W17 produced by a Ta (p,3n) reaction has also been extracted as the thiocyanate of W(lV) Into ethyl acetate (268). [Pg.36]

Aluminum acetate Aluminum caprylate Aluminum distearate Aluminum myristates/palmitates Aluminum stearate Aluminum tristearate N-2-Aminoethyl-3-aminopropyl trimethoxysilane Aminoethylethanolamine Aminomethyl propanol Aminopropyltriethoxysilane Aminopropyltrimethoxysilane Ammonium benzoate Ammonium borate Ammonium citrate dibasic Ammonium laureth sulfate Ammonium laureth-5 sulfate Ammonium laureth-7 sulfate Ammonium laureth-12 sulfate Ammonium laureth-30 sulfate Ammonium lauryl sulfate Ammonium maleic anhydride/diisobutylene copolymer Ammonium oleate Ammonium persulfate Ammonium polyacrylate Ammonium potassium hydrogen phosphate Ammonium stearate Ammonium sulfamate Ammonium thiocyanate Ammonium thiosulfate Amyl acetate Antimony trioxide Asbestos Asphalt Azelaic acid 2,2 -Azobisisobutyronitrile Barium acetate Barium peroxide Barium sulfatej Bentonite Benzalkonium chloride Benzene Benzethonium chloride Benzothiazyl disulfide Benzoyl peroxide Benzyl alcohol Benzyl benzoate 1,3-Bis (2-benzothiazolylmercaptomethyl) urea 1,2-Bis (3,5-di-t-butyl-4-hydroxyhydrocinnamoyl) hydrazine 4,4 -Bis (a,a-dimethylbenzyl) diphenylamine Bisphenol A Bis (trichloromethyl) sulfone Boric acid 2-Bromo-2-nitropropane-1,3-diol 1,4-Butanediol Butoxydiglycol Butoxyethanol Butoxyethanol acetate n-Butyl acetate Butyl acetyl ricinoleate Butyl alcohol Butyl benzoate Butyl benzyl phthalate Butyidecyl phthalate Butylene glycol t-Butyl hydroperoxide... [Pg.4796]

Ammonium thiocyanate s-Amyl alcohol Aniline m-Anisidine o-Anisidine p-Anisidine Anisole p-Anisyl alcohol Anthranilic acid Arsenic trichloride Benzaldehyde Benzalkonium bromide 1,2-Benzisothiazole Benzoquanamine Benzoin Benzopinacol Benzotrifluoride Benzoyl chloride N-Benzylamine Benzyl chloroform ate... [Pg.5406]

Thiourea, Thioureas Thiourea dioxide Selenourea Thiocyanates Dimethyl sulfate Dimethyl pyrosulfate Sulf oxonium salts Sulfonamides n-Butyl disulfide. Amyl disulfide, Benzyl disulfide... [Pg.749]


See other pages where N-Amyl thiocyanate is mentioned: [Pg.419]    [Pg.29]    [Pg.308]    [Pg.442]    [Pg.21]    [Pg.21]    [Pg.300]    [Pg.419]    [Pg.29]    [Pg.308]    [Pg.442]    [Pg.21]    [Pg.21]    [Pg.300]    [Pg.3257]    [Pg.698]    [Pg.38]    [Pg.139]    [Pg.51]    [Pg.5695]    [Pg.203]    [Pg.29]    [Pg.21]    [Pg.5688]   
See also in sourсe #XX -- [ Pg.21 ]

See also in sourсe #XX -- [ Pg.21 ]




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Amyl Thiocyanate

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