Process and products of purification of anhydrosugar alcohols
    2.
    发明授权
    Process and products of purification of anhydrosugar alcohols 有权
    脱氢葡萄糖醇的纯化方法和产物

    公开(公告)号:US06670033B1

    公开(公告)日:2003-12-30

    申请号:US09857574

    申请日:2001-11-27

    IPC分类号: D02G300

    摘要: A process for the formation of a purified anhydrosugar alcohol is disclosed, whereby the resultant purified anhydrosugar alcohol has a purity of at least 99.8% and is substantially colorless. The anhydrosugar alcohol is purified by distillation, recrystallization from methanol, ethanol or ethylene glycol, melt recrystallization, or a combination thereof. Preferably, the purification is by distillation followed by recrystallization from methanol, ethanol or ethylene glycol. A test for determining the purity of the anhydrosugar alcohol is disclosed, wherein the color of the anhydrosugar alcohol after annealing at a temperature of at least 260° C. for at least four hours is examined. Alternatively, purity can be determined by examination of ultraviolet (UV) transmittance of the purified anhydrosugar alcohol at various wavelengths. The purified anhydrosugar alcohol may be incorporated into a polymer such as a polyester, which may in turn be used to form such articles of manufacturing as containers, optical disks, fibers, sheets and films.

    摘要翻译: 公开了形成纯化的脱水葡萄糖醇的方法,由此得到的纯化的脱水葡萄糖醇的纯度至少为99.8%,基本上是无色的。 通过蒸馏纯化脱水葡萄糖醇,从甲醇,乙醇或乙二醇中重结晶,熔融重结晶或其组合。 优选地,通过蒸馏进行纯化,然后从甲醇,乙醇或乙二醇中重结晶。 公开了用于测定脱水葡萄糖醇纯度的试验,其中在至少260℃的温度下退火至少4小时后的脱水葡萄糖醇的颜色被检查。 或者,可以通过检查各种波长的纯化的脱水葡萄糖醇的紫外线(UV)透射率来确定纯度。 纯化的脱水葡萄糖醇可以掺入聚合物如聚酯中,聚酯可以依次用于形成容器,光盘,纤维,片和薄膜等制造品。

    Color control & stability in acetaminophen
    4.
    发明授权
    Color control & stability in acetaminophen 失效
    对乙酰氨基酚的色泽控制和稳定性

    公开(公告)号:US5399760A

    公开(公告)日:1995-03-21

    申请号:US105724

    申请日:1993-08-11

    CPC分类号: C07C231/24

    摘要: A method is provided for purifying crude N-acetyl-para-aminophenol (APAP) containing color bodies or their precursors, the method comprising: a) forming a solution of the crude APAP; and b) subsequently contacting the solution with substoichiometric quantifies of an acetylating agent for a sufficient period of time to convert said color bodies or their precursors to substantially non-color bodies/stable, colorless substances; said quantities of acetylating agent provided is such that substantially none of the APAP is converted to other compounds.

    摘要翻译: 提供了一种纯化含有着色体或其前体的粗N-乙酰基对氨基苯酚(APAP)的方法,该方法包括:a)形成粗APAP溶液; 和b)随后将所述溶液与乙酰化剂的亚化学计量定量充分一段时间,以将所述着色体或其前体转化成基本上非色体/稳定的无色物质; 所提供的所述量的乙酰化剂使得基本上没有APAP转化为其它化合物。

    Method for purification of ibuprofen comprising mixtures
    5.
    发明授权
    Method for purification of ibuprofen comprising mixtures 失效
    包含混合物的IBUPROFEN的方法

    公开(公告)号:US5151551A

    公开(公告)日:1992-09-29

    申请号:US579427

    申请日:1990-09-06

    IPC分类号: C07C51/43

    CPC分类号: C07C51/43

    摘要: This invention pertains to a method of purifying ibuprofen-comprising reaction product mixtures. The method of purification is based on crystallization of ibuprofen from a hydrocarbon solvent and the discovery that there are impurity complexes in the ibuprofen-comprising reaction product mixtures which cannot be removed by crystallization from a hydrocarbon solvent.The method of the invention includes at least one step in which the impurity complex in a first ibuprofen-comprising mixture is destabilized or broken up, followed by crystallization of the ibuprofen from a second solution or mixture comprising the first ibuprofen-comprising mixture, whereby the impurities which were previously complexed can then be removed from the ibuprofen by the crystallization of ibuprofen from a solvent.