Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Chief

White crystals, m.p. 114" C. Manufactured by reacting aniline with excess ethanoic acid or ethanoic anhydride. Chief use is in the manufacture of dye intermediates such as p-nitro-acetanilide, p-nitroaniline and p-phenylene-diamine, in the manufacture of rubber, and as a peroxide stabilizer. [Pg.10]

Agar occurs as a cell-wall constituent of the red marine algae Rho ophyceae, from which it is extracted by hot water, and marketed as a dry powder, flakes, or strips. It dissolves in hot water and sets on cooling to a jelly at a concentration as low as 0-5%. Its chief uses are as a solid medium for cultivating micro-organisms, as a thickener, emulsion stabilizer in the food industry and as a laxative. [Pg.17]

Its chief outlet is as an intermediate in the preparation of flavanthrene and indanthrene. [Pg.29]

Prepared by reduction of 4-nitrophenol or 4-nitrosophenoi. Can be diazotized and used as a first component in azo-dyes. Chief outlet is for sulphur dyes in which it is fused with sodium polysulphides. L/sed as a photographic developer. [Pg.30]

CioHi O. White leaflets, with a strong smell and sweet taste, m.p. 22 C, b.p. 235 C. The chief constituent of anise and fennel oils and other essential oils, from which it is manufactured. It can also be prepared from anisole (meihoxybenzene). It is widely used for flavouring pharmaceuticals and dentifrices, and in perfumery. [Pg.34]

Its chief importance is as a source of cinnamic acid by condensation with sodium ethan-oate and ethanoic anhydride and as a source of triphenylmethane dyestuffs by condensation with pyrogallol, dimethylaniline, etc. It is also used in the manufacture of perfumes. [Pg.54]

CCl3CH(OH)2, C3H3CI3O2. Crystallizes in large, colourless prisms having a peculiar odour m.p. 57"C, b.p. 91-5 C. Manufactured by adding the calculated amount of water to chloral. For other properties see chloral. Its chief use is as a hypnotic. [Pg.91]

Prepared by the direct nitration of naphthalene with a mixture of nitric and sulphuric acids. Its chief use was for the preparation of l-naphthyiamine and its derivatives. [Pg.279]

C21H36O2. M,p. 238°C. There are four isomeric pregnane-3,20-diols differing only in the orientation of the hydroxyl groups at positions 3 and 20 and with the 5/ configuration. Only the 3a,20a occurs naturally. It is formed by reduction of progesterone in the liver and is the chief urinary metabolite of it, being... [Pg.326]

The mixture of xylidines has been used as a first component of azo-dyes. The chief constituent of the mixture is m-xylidine (4-amino-1,3-xylene). It can be separated by crystallization from glacial ethanoic acid. It is also used for the preparation of azo-dyes. [Pg.430]

Various kinds of potentials have been referred to in the course of this and the preceding chapter, and their interrelation is the subject of the present section. The chief problem is that certain types of potential differences are physically meaningful in the sense that they are operationally defined, whereas others that may be spoken of more vaguely are really conceptual in nature and may not be definable experimentally. [Pg.205]

Generally speaking, intermolecular forces act over a short range. Were this not the case, the specific energy of a portion of matter would depend on its size quantities such as molar enthalpies of formation would be extensive variables On the other hand, the cumulative effects of these forces between macroscopic bodies extend over a rather long range and the discussion of such situations constitutes the chief subject of this chapter. [Pg.225]


See other pages where Chief is mentioned: [Pg.10]    [Pg.21]    [Pg.28]    [Pg.63]    [Pg.65]    [Pg.67]    [Pg.84]    [Pg.86]    [Pg.87]    [Pg.89]    [Pg.89]    [Pg.94]    [Pg.135]    [Pg.138]    [Pg.169]    [Pg.178]    [Pg.178]    [Pg.201]    [Pg.222]    [Pg.233]    [Pg.258]    [Pg.286]    [Pg.286]    [Pg.287]    [Pg.291]    [Pg.312]    [Pg.316]    [Pg.330]    [Pg.331]    [Pg.344]    [Pg.350]    [Pg.361]    [Pg.385]    [Pg.403]    [Pg.414]    [Pg.423]    [Pg.333]    [Pg.703]    [Pg.1209]   
See also in sourсe #XX -- [ Pg.6 , Pg.9 ]

See also in sourсe #XX -- [ Pg.26 , Pg.36 , Pg.70 , Pg.105 , Pg.314 ]




SEARCH



Assistant Chief, CWS, for Field Operations

Assistant Chief, CWS, for Materiel

British Chiefs of Staff

Chief Inspecting Officer of Railways

Chief Large Intestine)

Chief Liver

Chief Liver-blood deficiency

Chief Operating Officer

Chief Process Improvement Officer

Chief Ruler

Chief Safety Officer

Chief Scientific Officers

Chief aftermath

Chief cells

Chief cells granules

Chief cells pepsinogen

Chief cells pepsinogen secreted

Chief cells renewal

Chief damp-cold syndrome

Chief diversity officers

Chief executive officer

Chief feature

Chief financial officer

Chief heat syndrome

Chief information officer

Chief information technology officer

Chief internal organs

Chief marketing officer

Chief of Naval Operations

Chief of Ordnance

Chief of Transportation

Chief of the Defence Staff

Chief purchasing officer

Chief source

Chief syndromes

Chief technology officer

Chief wind-cold syndrome

Chief wind-heat syndrome

Chief, Chemical Corps

Chiefs of Staff

Combined Chiefs of Staff,

Copper chief

Finance/Administrative Section Chief

Joint Chiefs of Staff

Key Personnel Office of Chief, Chemical Warfare Service

Logistics Section Chief

Lord Chief Justice

Lung, heat syndrome chief

Natural Occurrence, Chief Minerals, and Ores

Neck chief cells

Operations Section Chief

Pepsinogen chief cell secretion

Planning Section Chief

Separation, solid-liquid chief mechanical means

Strychnine is the chief alkaloid present in nux vomica

Substances, chief

Warfare Service Chiefs

© 2024 chempedia.info