Sorbitol acetate

Performance criteria of clarifying agents are clarity, organoleptics, processability and nucleation. A typical third generation clarifying agent is the sorbitol acetal Millad 3988 (3,4-dimethyl dibenzylidene sorbitol). 

Clear antiperspirants have become popular because they leave no visible residue.They are not always formulated through a microemulsion route. Clear sticks can be based on dibenzylidene sorbitol acetal (DBSA) gelling agent and zirconium or glycine-complexed aluminum chlorhydrate antiperspirant actives that are soluble in propylene glycol without water. An alternative route is to closely match the refractive indices of the oil and water phases so a clear product (not a microemulsion) results for an antiperspirant gel [20,23]. Clear deodorant sticks with the active ingredient triclosan can be solidified with sodium stearate, which is incompatible with antiperspirant active ingredients (aluminium chlorhydrates). 

Synonyms Bis-0-(benzylidene)-D-glucitol Bis-o-(phenylmethylene)-D-glucitol D-Glucitol, bis-o-( phenyl methylene)- Sorbitol acetal... 

Sorbitol acetal. See Dibenzylidene sorbitol Sorbitol hexaethoxylate, stearate. See Sorbeth-6 hexastearate Sorbitol sol n. 

Most of the current clarifiers are sorbitol derivatives. They include Great Lakes Clearlite NU 005, and Ciba s Irgaclear additives, some of which are now manufactured by Roquette in France, as well as NC-4 sorbitol acetal clarifiers supplied by Mitsui Toatsu Chemicals in Japan. One exception is Dover Chemical s Doverlube FL-599, a polyethylene glycol ester offered for clarifying polypropylene and also as a process aid for high impact polystyrene. 

Conversion to acetates, trifluoroacetates (178), butyl boronates (179) trimethylsilyl derivatives, or cycHc acetals offers a means both for identifying individual compounds and for separating mixtures of polyols, chiefly by gas—Hquid chromatography (glc). Thus, sorbitol in bakery products is converted to the hexaacetate, separated, and determined by glc using a flame ionisation detector (180) aqueous solutions of sorbitol and mannitol are similarly separated and determined (181). Sorbitol may be identified by formation of its monobensylidene derivative (182) and mannitol by conversion to its hexaacetate (183). 

Zentner and coworkers [24,26] utilized this information in their development of a system that releases this drug over a 24 hr period. The use of NaCl to modulate the release of diltiazem presents an interesting problem in that the concentration of the solubility modifier must be maintained within certain limits and below its saturation solubility within the device. To solve this problem, core formulations were developed that contained both free and encapsulated NaCl. The encapsulated NaCl was prepared by placing a microporous coating of cellulose acetate butyrate containing 20 wt% sorbitol onto sieved NaCl crystals. The coated granules released NaCl over 12-14 hr period via an osmotic mechanism into either water or the core tablet formulation. The in vitro release profile for tablets (core I devices) containing 360 mg of diltiazem HC1 and 100 mg of NaCl equally divided between the immediate release and controlled release fractions... 

Arlitan was treated with p-toluenesulfonyl chloride, followed by acetic anhydride, in pyridine solution and the tosyltriacetylanhydro-D-sorbitol so obtained was then treated with sodium methoxide. The product of the reaction was l,4 3,6-dianhydro-D-sorbitol. Accordingly,... 

Chloro-6-desoxy-3,5-benzylidene-l,4-anhydro-D-sorbitol (XVI) possesses an unusual property in that the benzylidene group is removed by distillation in alkaline or neutral solution. From the neutral solution it was possible to isolate 6-chloro-6-desoxy-l,4-anhydro-D-sorbitol as its triacetyl derivative. At the same time diacetyl-1,4 3,6-dianhydro-D-sorbitol was also formed. This removal of an acetal residue from a... 

The acetates of the l,4 3,6-dianhydrohexitols may also be useful as plasticizers both 2,5-diacetyl-l,4 3,6-dianhydro-D-mannitol and the analogous D-sorbitol derivative have been described.97... 

In the Codex Alimentarius a number of further sequestrants and antioxidant synergists are issued which also pertain to the group of antioxidants. The main representatives of sequestrants are acetates, citrates, tartrates, phosphates, orthophosphates, diphosphates, triphosphates, and polyphosphates, esters of glycerol, sorbitol and sorbitol syrup, gluconates, and 1,4-heptonolactone. Lactates and tartaric acid are considered as antioxidant synergists. The spectrum... 

It should be noted that the following positions are synonymous in D- or L-mannitol and d- or L-iditol 1 and 6, 2 and 5, and 3 and 4. Sorbitol, because of lower optical symmetry, would form even more derivatives. The number of possible acetals is much smaller and that of metallic complexes still smaller. The number of various theoretical permutations of mixed ether-esters, ether-acetals, etc., utilizing readily available reagents, runs into the hundreds of thousands. 

Saline laxatives like MgS04, Mg(OH)2, Mg2 Citrate and Na+ Phosphates act via their osmotic pressure to retain water in the colon. Other osmotic laxatives are carbohydrates such as lactulose, glycerin, sorbitol, and mannitol. They are not absorbed and are resistant to digestion in the small intestine. Most agents are orally administered. It should be noted however that glycerin, sodium phosphates and sorbitol are formulated for rectal use. From lactulose lactic and acetic acids are formed by intestinal bacteria and apart from its osmotic effects it thus acidifies the content of the colon. The reduction of the pH stimulates motility and secretion. 

Osmotic laxatives (e.g., lactulose, sorbitol) are poorly absorbed or nonabsorbable compounds that draw additional fluid into the GI tract. Lumen osmolality increases, and fluid movement occurs secondary to osmotic pressure. Lactulose is a synthetic disaccharide that is poorly absorbed from the GI tract, since no mammalian enzyme is capable of hydrolyzing it to its monosaccharide components. It therefore reaches the colon unchanged and is metabolized by colonic bacteria to lactic acid and to small quantities of formic and acetic acids. Since lactulose does contain galactose, it is contraindicated in patients who require a galactose-free diet. Metabolism of lactulose by intestinal bacteria may result in increased formation of intraluminal gas and abdominal distention. Lactulose is also used in the treatment of hepatic encephalopathy. 

Furfuryl Alcohol Furfuryl Alcohol Furfuryl Alcohol Isoamyl Alcohol Formaldehyde Solution Gallic Acid Gallic Acid Tannic Acid Tannic Acid Benzene Hexachloride Gas Oil Cracked Copper Nitrate Benzene Hexachloride Acetic Acid Sorbitol... 

Proteases have received less attention than lipases, but in one of the earliest papers on biocatalysis in ionic liquids it was noted that the activity loss of thermo-lysin during preincubation proceeded much more slowly in [BMIm][PF6] than in ethyl acetate [8]. The storage stability of a-chymotrypsin in the ionic liquid [EMIm][ Tf2N] was compared with that in water, 3 M sorbitol, and 1-propanol. The residual hydrolytic activity (after dilution with aqueous buffer) was measured vs time, and structural changes were monitored by fluorescence and CD spectroscopy as well as DSC [98]. The enzyme s life-time in [EMIm][ Tf2N] at 30°C was more than twice that in 3 M sorbitol, six times as long as that in water, and 96 times as long as that in 1-propanol. 

Mannitol hexanitrate is obtained by nitration of mannitol with mixed nitric and sulfuric acids. Similarly, nitration of sorbitol using mixed acid produces the hexanitrate when the reaction is conducted at 0—3°C and at —10 to —75°C, the main product is sorbitol pentanitrate (117). Xylitol, ribitol, and L-arabinitol are converted to the pentanitrates by fuming nitric acid and acetic anhydride (118). Phosphate esters of sugar alcohols are obtained by the action of phosphorus oxychloride (119) and by alcoholysis of organic phosphates (120). The 1,6-dibenzene sulfonate of D-mannitol is obtained by the action of benzene sulfonyl chloride in pyridine at 0°C (121). To obtain 1,6-dimethanesulfonyl-D-mannitol free from anhydrides and other by-products, after similar sulfonation with methane sulfonyl chloride and pyridine the remaining hydroxyl groups are acetylated with acetic anhydride and the insoluble acetyl derivative is separated, followed by deacetylation with hydrogen chloride in methanol (122). Alkyl sulfate esters of polyhydric alcohols result from the action of sulfur trioxide—trialkyl phosphates as in the reaction of sorbitol at 34—40°C with sulfur trioxide—triethyl phosphate to form sorbitol hexa(ethylsulfate) (123). 

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