摘要:
A process is provided for preparing C8-C22 acyl amido compounds via reaction in a polyol (molecular weight 76 to 400) of interesterifying a C1-C3 alkyl ester of a C5-C22 fatty acid with an amino compound or salt thereof. The resultant mass of material will have a Hunter Lab Color Scale value L ranging from 70 to 100.
摘要:
A reagent composition for forming fatty acyl amido surfactants is provided which includes an alkali metal or alkaline earth metal salt of an amino compound; a polyol of molecular weight ranging from 76 to 300; and no more than 10% water.
摘要:
A process is provided for preparing C8-C22 acyl amido compounds via reaction in a polyol (molecular weight 76 to 400) of interesterifying a fatty acid ester with an amino compound or salt thereof. The resultant mass of material will have a Hunter Lab Color Scale value L ranging from 70 to 100.
摘要翻译:提供了通过使脂肪酸酯与氨基化合物或其盐进行酯交换的多元醇(分子量76〜400)中的反应来制备C8-C22酰基酰胺化合物的方法。 所得材料的质量将具有70至100的Hunter Lab Color Scale值L。
摘要:
A surfactant concentrate is provided that includes C8-C22 acyl amido compounds, a polyol and C8-C22 fatty acids. The concentrate is formed via an interesterification reaction between a C1-C3 alkyl ester of a C8-C22 fatty acid and an amino compound or salt thereof in a polyol. The resultant surfactant concentrate will have a Hunter Lab Color Scale value L ranging from 70 to 100.
摘要翻译:提供表面活性剂浓缩物,其包括C8-C22酰基酰胺化合物,多元醇和C 8 -C 22脂肪酸。 浓缩物通过C8-C22脂肪酸的C1-C3烷基酯与多元醇中的氨基化合物或其盐之间的酯交换反应形成。 所得的表面活性剂浓缩物将具有70至100的Hunter Lab Color Scale值L。
摘要:
Oil-in-water emulsions can be formed using surfactants with biospecific headgroups. Emulsion droplets adhere to surfaces of microorganisms or to various biological surface bearing appropriate adhesins, thus delivering surfactant materials directly to various surfaces. Lipophilic materials and essential oils can be targeted in this way. The emulsions may be incorporated into oral hygiene non-food compositions or compositions for topical application to skin, hair or nails.
摘要:
N-substituted aldonamides are synthesized by the reaction of alkylamines and aldonolactone. Commercially available sources of aldonolactones (e.g., lactobiono-1,5-lactone) include aldonic acid (e.g., lactobionic acid). The presence of the acid leads to the formation of an ammonium salt impurity. The ammonium salt formation during the synthesis of N-alkyl aldonamides was minimized by the addition of an external acid. External acids and, optionally, emulsifiers were utilized to substantially reduce or eliminate the formation of an ammonium salt and to obtain N-substituted aldonamides of high purity.
摘要:
Stabilized cationic ammonium compounds are described. The compounds are stabilized with pyridine-based chelators and/or heteroketo-based chelators that impede the generation of nitrogen comprising groups from the cationic ammonium compounds.
摘要:
Stabilized cationic ammonium compounds are described. The compounds are stabilized with pyridine-based chelators and/or heteroketo-based chelators that impede the generation of nitrogen comprising groups from the cationic ammonium compounds.
摘要:
The present invention relates to a detergent composition comprising:(1) 5% to 95% by wt. anionic surfactant; and(2) 5% to 95% by wt. of a detergent surfactant mixture comprising:(a) a nonionic surfactant having an average degree of alkoxylation of 6 to 10; and(b) an aldobionamide.
摘要:
A process of preparing aldobionamides and N-substituted aldobionamides which includes the steps of recovering a by-product of the process (an ammonium salt of an aldobionic acid) and converting it into at least one starting material. Aldobiono-1,5-lactone is reacted with a primary or secondary amine and the resulting solution containing the by-product of the reaction is passed through an anionic exchange column to obtain the eluate containing the starting amine and some aldobionamide. The eluate may be recycled as part of the starting material mixture. Alternatively, the amine and the aldobionamide may be recovered from the eluate, and the amine alone may be recycled. Aldobionate anion is retained on the column and may be converted into the salt of an aldobionic acid and then into the aldobionic acid.