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Amyl chloride

Boiling point Tiro point Flaih point [Pg.103]

ntent heat of vaporization Specific gravity 2S/2S C Specific heat Refractive index 25 C Viicoiity 25 C Weight par gallon Q2S C [Pg.103]

Chlor-. of or combined with chlorine, chloro (as Chlorbenzoeadure, chlorobenzoic acid), chloride of (as Chlorzink, zinc chloride), chlorahnlich, a. like chlorine, chlorinous. Chlor-alaun, m. chloralum, -alkalien, n.pl. alkali-metal chlorides, -allyl, n, allyl chloride, -aluminium, n. aluminum chloride, -ammon, m., -ammonium, n. ammonium chloride, -amyl, n, amyl chloride, -antimon, n, antimony chloride, -arsenlk, n. chloride of arsenic, -arsenikldsung, /, (Pkarm.) solution of arsenious add, hydrochloric solution of arsenic, -arsinkampfstoff, m. chlorodi-phenylarsine, adamsite, chlorartig, a. like chlorine, chlorinous,... [Pg.90]

Adipic acid Unknown s Amyl chloride Unknown 1... [Pg.263]

Isoamyl ether and -amyl ether formed In preparation of amyl alcohols from amyl chloride very slightly soluble In water used mainly as a solvent. am-al e-thar) amyl mercaptan org chem C5H11SH A colorless to light yellow liquid with a boiling range of 104-130°C soluble In alcohol used In odorant for detecting gas line leaks. am-ol mor kapitan ... [Pg.23]

Alkylation of benzene is old technology. The French chemist, Charles Friedel, with his American partner, James Crafts, in 1877, stumbled (almost literally) across the technique for alkylating benzene with amyl chloride (C5H11CI). The use of a metallic catalyst, in this case aluminum, was the key. The Friedel-Crafts reaction is classical and remains a principal route for alkylating benzene with ethylene to make EB. [Pg.120]

The specific rates of hydrolysis of five organic halides in three water-based liquid mixtures near their respective equilibrium consolute points have been observed to be suppressed. The systems studied included t-amyl chloride in isobutyric acid water (upper consolute temperature), and 3-chloro-3-methylpentane in 2-butoxyethanol water (lower consolute temperature). The slowing effect occurred within a few tenths of a degree on either side of the consolute temperature. [Pg.341]

Tertiary alkyl halides undergo a series of reactions when treated with hydrogen fluoride. f-Amyl chloride by means of reactions catalyzed by hydrogen fluoride yielded a series of teritary chlorides including f-butyl chloride (Simons et al., 35). t-Butyl chloride gives the same series of... [Pg.215]

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]

See other pages where Amyl chloride is mentioned: [Pg.273]    [Pg.273]    [Pg.274]    [Pg.276]    [Pg.373]    [Pg.112]    [Pg.112]    [Pg.112]    [Pg.61]    [Pg.199]    [Pg.107]    [Pg.145]    [Pg.147]    [Pg.488]    [Pg.145]    [Pg.30]    [Pg.61]    [Pg.273]    [Pg.273]    [Pg.274]    [Pg.276]    [Pg.61]    [Pg.61]    [Pg.37]    [Pg.613]    [Pg.97]    [Pg.569]    [Pg.97]    [Pg.973]    [Pg.704]    [Pg.704]    [Pg.723]    [Pg.723]    [Pg.286]    [Pg.345]    [Pg.1715]    [Pg.242]    [Pg.127]    [Pg.211]    [Pg.216]    [Pg.22]   
See also in sourсe #XX -- [ Pg.178 ]



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Amyl mercuric chloride

Chloropentane (-Amyl chloride)

Iso-Amyl chloride

Mixed Amyl Chlorides

N-Amyl chloride

T-Amyl chloride

Tert.-Amyl chloride

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