Big Chemical Encyclopedia

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

Articles Figures Tables About

Ricinoleic acid esters

The starting point for this amino acid, from which nylon 11 is obtained, is the vegetable product castor oil, composed largely of the triglyceride of ricinoleic acid. This is first subjected to treatment with methanol or ethanol to form the appropriate ricinoleic acid ester. [Pg.483]

Hayes, D.G. Lipase-catalyzed synthesis of poly-hydric alcohol-poly(ricinoleic acid) ester star polymers. Polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.) 2005, 46 (1), 276-277. [Pg.3190]

Sulfated Natural Oils and Fats. Sulfated natural triglycerides were the first nonsoap commercial surfactants introduced in the middle of the nineteenth century. Since then sulfates of many vegetable, animal, and fish oils have been investigated (see also Fats AND FATTY oils). With its hydroxyl group and a double bond, ricinoleic acid (12-hydroxy-9,10-octadecenoic acid) is an oil constituent particularly suited for sulfation. Its sulfate is known as turkey-red oil. Oleic acid is also suited for sulfation. Esters of these acids can be sulfated with a minimum of hydrolysis of the glyceride group. Polyunsaturated acids, with several double bonds, lead to dark-colored sulfation products. The reaction with sulfuric acid proceeds through either the hydroxyl or the double bond. The sulfuric acid half ester thus formed is neutralized with caustic soda ... [Pg.244]

Castor oil sulfation results largely in a sulfuric acid ester in which the hydroxyl group of ricinoleic acid has been esterified. However, other reactions can also take place. For example, the double bond can be attacked to produce an ester or the hydroxysulfonic acid (33). Hydrolysis of the sulfuric acid esters occurs during the reaction and subsequent treatment forming hydroxy acids and sulfuric acid. These hydroxy acids can be further sulfated. [Pg.154]

Pyrolytic Decomposition. The pyrolytic decomposition at 350—460°C of castor oil or the methyl ester of ricinoleic acid spHts the ricinoleate molecule at the hydroxyl group forming heptaldehyde and undecylenic acids. Heptaldehyde, used in the manufacture of synthetic flavors and fragrances (see Elavors and spices Perfumes) may also be converted to heptanoic acid by various oxidation techniques and to heptyl alcohol by catalytic hydrogenation. When heptaldehyde reacts with benzaldehyde, amyl cinnamic aldehyde is produced (see Cinnamic acid, cinnamaldehyde, and cinnamyl... [Pg.154]

Ricinoleic acid (dl 12-hydroxyoleic acid) [14I-22-0J M 298.5, m 7-8° (a-form), 5.0° (7-form), n 1.4717, pKe, -4.5. Purified as methyl acetylricinoleate [Rider J Am Chem Soc 53 4130 1931], fractionally distilling at 180-185°/0.3mm, then 87g of this ester was refluxed with KOH (56g), water (25mL), and MeOH (250mL) for lOmin. The free acid was separated, crystd from acetone at -50°, and distd in small batches, b 180°/0.005mm. [Bailey et al. J Chem Soc 3027 1957.]... [Pg.349]

Oleic acid, linolic acid, ricinolic acid, and 2-bromostearic acid methyl ester as well are reacting with diethyl phosphite in the presence of benzoyl peroxide to the corresponding phosphono fatty acid esters [156-158]. [Pg.584]

The important but unusual fatty acid ricinoleic acid, or 12-hydroxyoleic acid, is a major component of castor oil (>87%) and is also found in useful quantities in ergot. The metal salts of the acid find use in dry-cleaning soaps but the majority is converted to aminoundecanoic acid (Scheme 6.6) which is used to make nylon 11. Nylon 11 has very good chemical and shock-resistance properties, which have led to it being used in the automotive industry. Ricinoleic triglyceride is initially transesterified to the methyl ester. This is heated to 300 °C at which temperature it is... [Pg.188]

Another class of PSA-fatty acid-based copolymers has been synthesized from the ricinoleic acid and ricinoleic half-esters with maleic and succinic anhydride, poly(sebacic-co-ricinoleic acid maleate), poly(sebacic-co-ricinoleic acid succinate), and poly(sebacic-co-12-hydroxystearic acid succinate) (P(SA-RAM), P(SA-RAS), and P(SA-HSAS)) (Krasko et al., 2003 Teomim et al., 1999). These syntheses result in poly(anhydride-co-esters). [Pg.179]

One of the more advanced technical offerings from castor oil is a line of polyester diols, triols, and higher functional polyols derived from 100% castor oil as products for the preparation of polyurethane prepolymers and elastomers [68]. The Polycin line of polyols are prepared by transesterification of ricinoleic acid and derivatives. The producers (Vertellus) offer diol and triol products, as well as a recently developed series of diol and triol glyceryl ricinoleate esters that are stated to be prepared from 100% castor oil, making them fully renewable in content. The products are recommended for coatings, sealants, and adhesive applications. [Pg.329]

Ricinoleic acid (Figure 3.8) is the major fatty acid found in castor oil from seeds of the castor oil plant (Ricinus communis Euphorbiaceae), and is the 12-hydroxy derivative of oleic acid. It is formed by direct hydroxylation of oleic acid (usually esterified as part of a phospholipid) by the action of an 02- and NADPH-dependent mixed function oxidase, but this is not of the cytochrome P-450 type. Castor oil has a long history of use as a domestic purgative, but it is now mainly employed as a cream base. Undecenoic acid (A9-undecenoic acid) can be obtained from ricinoleic acid by thermal degradation, and as the zinc salt or in ester form is used in fungistatic preparations. [Pg.47]

Glycerol Esters of Condensed Castor Oil Fatty Acids Polyglycerol Esters of Interesterified Ricinoleic Acid Polyglycerol Polyricinoleate... [Pg.343]

Teomim et al. [406] reported the synthesis of ricinoleic acid and hydrogenated ricinoleic acid (hydroxystearic acid)-based monomers, which were synthesized from the attachment of a carboxylic acid side chain via a hydrolyzable ester bond to the hydroxy group (succinic acid/maleic acid). These monomers were... [Pg.105]

Ricinoleic acid is a bifunctional fatty acid containing a hydroxy group along the fatty chain. The presence of both carboxylic and hydroxyl groups allows incorporation of ricinoleic acid into a polymer backbone by formation of an ester bond. The synthesis of poly(ester-anhydride) contains two steps trans-... [Pg.90]


See other pages where Ricinoleic acid esters is mentioned: [Pg.34]    [Pg.84]    [Pg.34]    [Pg.84]    [Pg.85]    [Pg.132]    [Pg.154]    [Pg.261]    [Pg.190]    [Pg.200]    [Pg.200]    [Pg.261]    [Pg.271]    [Pg.556]    [Pg.1316]    [Pg.297]    [Pg.5]    [Pg.194]    [Pg.115]    [Pg.106]    [Pg.91]    [Pg.269]    [Pg.530]   


SEARCH



Polyglycerol Esters of Interesterified Ricinoleic Acid

Ricinolate

Ricinoleate

Ricinoleates

Ricinoleic acid reaction with malonic esters

Ricinolic acid

© 2024 chempedia.info