Big Chemical Encyclopedia

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

Articles Figures Tables About

Stearic acid ethyl ester

Synonyms Ethyl octadecanoate Stearic acid ethyl ester Source Crampon, C. Charbit, G. Neau, E. [Pg.348]

Beilstein Handbook Reference) A13-01781 BRN 1788183 EINECS 203-887-4 Ethyl octadecanoate Ethyl stearate FEMA No, 3490 NSC 8919 Octadecanolc acid, ethyl ester Radia 7185 Stearic acid, ethyl ester. Chemical Intermediate, chemical synthesis lubricant in mineral, cutting, lamination, textile oils, and rust inhibitors textile and leather application also as emollient, plasticizer, solubilizer of active components in cosmetics and pharmaceuticals. Solid mp = 33° bpts = 213-215°, bpio = 199° insoluble in H2O, soluble in EtOH, Et20, CHCI3, very soluble in MezCO, Fina Chemicals. [Pg.280]

Stearic acid, dodecyl ester. See Lauryl stearate Stearic acid ester with lactate of lactic acid calcium salt. See Calcium stearoyl lactylate Stearic acid, ester with lactic acid bimol. ester, sodium salt. See Sodium stearoyl lactylate Stearic acid, ethylenediamine diamide. See Ethylene distearamide Stearic acid, ethyl ester. See Ethyl stearate Stearic acid, 2-ethylhexyl ester. See Octyl stearate... [Pg.4204]

Synonyms Ethyl octadecanoate Ethyl n-octadecanote Octadecanoic acid, ethyl ester Stearic acid, ethyl ester Definition Ester of ethyl alcohol and stearic acid Empirical C20H40O2 Formula CH3(CH2)ieCOOCH2CH3... [Pg.2126]

Stearic acid, ethyl ester. See Ethyl stearate... [Pg.2475]

Ethylcellulose is compatible with the following plasticizers dibutyl phthalate diethyl phthalate dibutyl sebacate triethyl citrate tributyl citrate acetylated monoglyceride acetyl tributyl citrate triacetin dimethyl phthalate benzyl benzoate butyl and glycol esters of fatty acids refined mineral oils oleic acid stearic acid ethyl alcohol stearyl alcohol castor oil corn oil and camphor. [Pg.281]

Sorbitan Monostearate occurs as an off white to tan colored, hard, waxy solid. It is a mixture of partial stearic and palmitic acid esters of sorbitol and its mono- and dianhydrides. It is manufactured by reacting edible commercial stearic acid (usually containing associated fatty acids, chiefly palmitic) with sorbitol. It is soluble at temperatures above its melting point in toluene, dioxane, ether, ethanol, methanol, and aniline. It is insoluble in cold water, and in mineral spirits and acetone, but is dispersible in warm water and soluble, with haze, above 50° in mineral oil and in ethyl acetate. [Pg.442]

Ethyl linoleate is prepared by debromination of the tetra-bromide by action of zinc, or nascent hydrogen from zinc and glacial acetic acid 3 by zinc and alcoholic-hydrochloric acid 2, 4 and by zinc and alcoholic-sulfuric acid.5 The pure acid can be obtained by saponification of the ester, and directly by action of zinc and pyridine (quinoline, aniline, piperidine) on tetrabromo-stearic acid.6... [Pg.101]

HKJOOO CAS 106-11-6 HR 3 2-(2-HYDROXYETHOXY)ETHYL ESTER STEARIC ACID... [Pg.754]

HYDROXYETHOXY)ETHYL ESTER STEARIC ACID see HKJOOO... [Pg.1723]

The sodium or potassium salt of palmitic acid, or of stearic acid or the mixed salts of several acids obtained from ordinary fats, is the common substance known as soap. This particular reaction of hydrolysis, is, therefore, known, also, as a reaction of saponification (soap formation). Strictly speaking the reaction of saponification applies only to the alkaline hydrolysis of fats, i,e., of glycerol esters, but, as the hydrolysis of other esters is a reaction of exactly the same character, the term is used to apply equally to the hydrolysis of any ester in presence of an alkali. In the case of the lower alcohol and lower acid esters, e.g., ethyl acetate, the salt formed is not a soap but is a crystalline salt, sodium acetate. [Pg.206]

Fatty-acids, salts and esters Aluminum monostearate, calcium stearate, ethyl oleate, isopropyl myristate, isopropyl palmitate, magnesium stearate, oleic acid, polyoxyl 40 stearate, proprionic acid, sodium stearate, stearic acid, purified stearic acid, and zinc stearate... [Pg.980]

Sommelet reaction, 33, 93 Sorbic acid, 5-hydroxy-/3-methyl, J-lactone, 32, 57 Stannic chloride, 33, 91 Stearic acid, 34, 15 Stearone, 33, 84 cis-Stilbene, 33, 88 fraws-Stilbene, 33, 89 Stirrer, for caustic fusion, 30, 104, 105 seal for, 30, 54 Stobbe condensation, 30, 18 Styrene, 33, 72 34, 85 reaction with sulfuric acid, 35, 83 Styrene dibromide, 30, 73 Styrene oxide, 31, 3 0-Styrenesulfonyl chloride, 34, 85 Succinic acid, 34, 44 Succinic acid, < -benzhydrylidene-, a-ETHYL ESTER, 30, 18 CLNNAMYL-, 31, 85 DIPHENYL ESTER, 34, 44 HEPTANOYL-, DIETHYL ESTER, 34, 51 PHENYL-, 30, 83 Succinic anhydride, 34, 40 SUCCINONITRILE, a, -DIPHENYL-, 32, 63 Sulfide, methyl 2-thienyl, 35, 85 Sulfonation of styrene, 34, 85 Sulfonyl chloride, from sodium sulfonate, 34, 85... [Pg.61]


See other pages where Stearic acid ethyl ester is mentioned: [Pg.415]    [Pg.880]    [Pg.955]    [Pg.1094]    [Pg.1776]    [Pg.415]    [Pg.880]    [Pg.955]    [Pg.1094]    [Pg.1776]    [Pg.2475]    [Pg.91]    [Pg.374]    [Pg.133]    [Pg.49]    [Pg.417]    [Pg.96]    [Pg.1540]    [Pg.374]    [Pg.628]    [Pg.1879]    [Pg.907]    [Pg.335]    [Pg.188]    [Pg.49]    [Pg.499]    [Pg.25]    [Pg.133]    [Pg.468]    [Pg.57]    [Pg.211]    [Pg.273]   
See also in sourсe #XX -- [ Pg.348 ]




SEARCH



Stearic

Stearic acid

© 2024 chempedia.info