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Methyl enanthate

Methyldinitrophenol, d715, d716 Methyl enanthate, m266 Methylene bromide, dl 10 Methylene bromochloride, b305 Methylene chloride, d235... [Pg.267]

Methyl enanthate. See Methyl heptanoate Methylene acetone. See Methyl vinyl ketone Methylene bichloride. See Methylene chloride... [Pg.2616]

Synonyms Heptanoic acid methyl ester Methyl enanthate Methyl heptoate Methyl n-heptylate Methyl oenanthylate... [Pg.2636]

Enanthaldehyde, -METHYL-/3-OXO-, DIMETHYL ACETAL, 32, 79 Enanthic acid, e-oxo, 31, 3 Epichlorohydrin, 31, 1 Esterification, by azeotropic distillation with toluene, 30, 30, 31 of ethanol with phosphorus trichloride, 31, 111... [Pg.55]

Testosterone (T.) derivatives for clinical use. T. esters for im. depot injection are T. propionate and T. heptanoate (or enanthate). These are given in oily solution by deep intramuscular injection. Upon diffusion of the ester from the depot, esterases quickly split off the acyl residue, to yield free T. With increasing lipophilicity, esters will tend to remain in the depot, and the duration of action therefore lengthens. A T. ester for oral use is the undecanoate. Owing to the fatty acid nature of undecanoic acid, this ester is absorbed into the lymph, enabling it to bypass the liver and enter, via the thoracic duct, the general circulation. 17-0 Methyltestosterone is effective by the oral route due to its increased metabolic stability, but because of the hepatotoxicity of Cl 7-alkylated androgens (cholestasis, tumors) its use should be avoided. Orally active mesterolone is 1 a-methyl-dihydrotestosterone. Trans-dermal delivery systems for T. are also available. [Pg.252]

Benzyl alcohol o-Anisidine Enanthic acid 2-[2- (2-Methoxyethoxy ) -ethoxy]-ethanol Methyl salicylate... [Pg.369]

Pyrocatechol Dipropylene glycol a-Trichlorotoluene m-Nitrotoluene p-Nitrotoluene o-Anisidine Enanthic acid Methyl salicylate p-Ethylphenol 3,4-Xylenol o-Phenetidine... [Pg.302]

Fluphenazine enanthate, like its parent compound fluphenazine hydrochloride is light sensitive. Exposure of a 10% solution of fluphenazine enanthate in iso-butyl methyl ketone for one month resulted in 5% decomposition. The mechanism of light catalyzed decomposition is probably similar to that of fluphenazine hydrochloride(see Analytical Profile). Fluphenazine enanthate hydrolyzes to fluphenazine in alkaline medium. [Pg.257]

C8H16O2 106-73-0 Enanthic acid methyl ester see Methyl heptanoate... [Pg.35]

C8H16O2 106-73-0 Methyl heptanoate syn. nMethyl enanthate nHeptanoic acid methyl ester nEnanthic acid methyl ester Oenanthic acid methyl ester nMethyl oenanthate... [Pg.41]

See other pages where Methyl enanthate is mentioned: [Pg.1268]    [Pg.299]    [Pg.256]    [Pg.256]    [Pg.563]    [Pg.41]    [Pg.1268]    [Pg.299]    [Pg.256]    [Pg.256]    [Pg.563]    [Pg.41]    [Pg.568]    [Pg.72]    [Pg.679]    [Pg.369]    [Pg.428]    [Pg.214]   
See also in sourсe #XX -- [ Pg.125 , Pg.256 ]



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