CAS: 5793-88-4; Calcium (2R,3S,4S,5S)-2,3,4,5-Tetrahydroxyhexanedioate

该化合物是一种化学化合物,它是由钙离子与沙酸反应形成的,一种糖酸,是糖氧化后产生的酸,通常作为白色粉末和白外粉接触,在水中可溶解,因而在各种应用中有用;该化合物以其在食品工业中的作用而著称,特别是作为稳定剂和厚度剂.此外,钙园区在药品和饮食补充方面有潜在用途,其化学结构特征是钙与酸盐离子相协调,有助于其功能性能.该化合物一般被视为安全的消费,但与任何添加剂一样,应在既定准则范围内使用.与许多钙盐一样,它也可以在钙补充,支持骨质健康和代谢功能方面发挥作用.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

合成工艺路线路线简述

    📜Calcium Gluconate 在 Sodium Hypochlorite,2,2,6,6-四甲基哌啶氧化物,水,Sodium Bromide体系中,反应 2.0H,以82.8%的收率获得calcium D-Glucarate
    参考文献:葡萄糖二酸钙的制备方法
    标题:葡萄糖二酸钙的制备方法
    摘要:本发明属于制药领域,具体涉及一种葡萄糖二酸钙的制备方法.所述的葡萄糖二酸钙的制备方法,将d‑葡萄糖酸盐加入反应容器中,降温至‑30‑50°C,加入催化剂,溶剂和氧化剂,进行催化氧化反应,得到葡萄糖二酸盐溶液;将葡萄糖二酸盐溶液与钙盐进行反应,得葡萄糖二酸钙;其中,所述的d‑葡萄糖酸盐为d‑葡萄糖酸钠,D‑葡萄糖酸锂,D‑葡萄糖酸钾,D‑葡萄糖酸钙,D‑葡萄糖酸镁或d‑葡萄糖酸锌.本发明采用d‑葡萄糖酸盐为原料,氧化剂用量少,操作简单,收率高,产品符合国内外药用辅料的质量要求,生产成本低,工业三废少,适合工业生产,对环境无污染.

    海关参考信息

    专利信息


    专利号:US-2006084800-A1
    优先权日:2004-06-30
    标 题 :Synthesis of aldonolactones, aldarolactones, and aldarodilactones using azeotropic distillation
    发明人:CHENAULT HENRY K
    权利人:CHENAULT HENRY K
    摘要:Processes for making lactones and dilactones from aldaric acids, aldonic acids, and their corresponding salts by dehydrative cyclization and azeotropic distillation. The processes can be carried out in the presence of water because water is removed by azeotropic distillation.

    专利号:WO-2006005071-A1
    优先权日:2004-06-30
    标题:Synthesis of aldonolactones, aldarolactones, and aldarodilactones using azeotrophic distillation
    发明人:CHENAULT H KEITH
    权利人:DU PONT; CHENAULT H KEITH
    摘要:Processes for making lactones and dilactones from aldaric acids, aldonic acids, and their corresponding salts by dehydrative cyclization and azeotropic distillation. The processes can be carried out in the presence of water because water is removed by azeotropic distillation.

    专利号:US-7550510-B2
    优先权日:2001-07-06
    标 题 :Solid phase synthesis of arylretinamides
    发明人:CURLEY JR ROBERT W; MERSHON SERENA M; BARNETT DEREK W; CLAGETT-DAME MARGARET; CHAPMAN JASON S
    权利人:WISCONSIN ALUMNI RES FOUND
    摘要:A solid phase synthetic method for preparing arylretinamides is provided. The method comprises reacting hexachloroacetone with a solvent-suspended resin-bound triphenylphosphine to provide a suspension comprising an activated chlorinating reagent; reacting retinoic acid with the activated chlorinating reagent to provide retinoyl chloride; adding pyridine and a select arylamine to the resulting mixture; and stirring the resulting mixture for a time and at a temperature sufficient for the select arylamine to react with the retinoyl chloride and provide the arylretinamide. Also provided, are select arylretinamides that can be prepared by the present method, and methods of using such arylretinamides to induce apoptosis in cancer cells.

    专利号:US-2004102650-A1
    优先权日:2001-07-06
    标 题:Solid phase synthesis of arylretinamides

    专利号:US-2006084817-A1
    优先权日:2004-06-30
    标 题 :Synthesis of aldonolactones, aldarolactones, and aldarodilactones using gas sparging
    发明人:CHENAULT HENRY K
    权利人:CHENAULT HENRY K
    摘要:Aldaric acids, aldonic acids, and their corresponding salts are cyclized to the corresponding lactone or dilactone using gas sparging to remove water.

    专利号:WO-2006005070-A1
    优先权日:2004-06-30
    标题 :Synthesis of aldonolactones, aldarolactones, and aldarodilactones using gas sparging

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S13 | EUCOSMETICS | Combined Inventory of Ingredients Employed in Cosmetic Products (2000) and Revised Inventory (2006) | DOI:10.5281/zenodo.2624118
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