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4,4'-{[3-(Octadecanoyloxy)propane-1,2-diyl]bis(oxy)}bis[2,3-bis(acetyloxy)-4-oxobutanoic acid] | 99670-21-0

中文名称
——
中文别名
——
英文名称
4,4'-{[3-(Octadecanoyloxy)propane-1,2-diyl]bis(oxy)}bis[2,3-bis(acetyloxy)-4-oxobutanoic acid]
英文别名
2,3-diacetyloxy-4-[2-(2,3-diacetyloxy-3-carboxypropanoyl)oxy-3-octadecanoyloxypropoxy]-4-oxobutanoic acid
4,4'-{[3-(Octadecanoyloxy)propane-1,2-diyl]bis(oxy)}bis[2,3-bis(acetyloxy)-4-oxobutanoic acid]化学式
CAS
99670-21-0
化学式
C37H58O18
mdl
——
分子量
790.8
InChiKey
MGNDTAFZQITDRD-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.3
  • 重原子数:
    55
  • 可旋转键数:
    38
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    259
  • 氢给体数:
    2
  • 氢受体数:
    18

文献信息

  • Method for the preparation of diacetyl tartaric acid esters of mono-and di-glycerides
    申请人:Liu Gaofeng
    公开号:US20120058232A1
    公开(公告)日:2012-03-08
    The present invention provides a method for the preparation of diacetyl tartaric acid esters of mono- and di-glycerides, which comprises steps of: adding L-tartaric acid and/or DL-tartaric acid and acetic anhydride into a reaction kettle, adding concentrated phosphoric acid as catalyst and mixing together to form a reaction system; heating the reaction kettle until a temperature of the reaction system reaches 50° C.˜55° C. to initiate a reaction, after the temperature of the reaction system rises and then drops to 80° C.˜90° C., keeping the temperature at 80° C.˜90° C. for 20˜60 min to obtain an intermediate product; adding stearic acid esters of mono- and di-glycerides to the intermediate product, then adding powdery sodium hydroxide as catalyst, controlling an inner pressure of the reaction kettle at −0.09 Mpa˜−0.098 Mpa, heating the reaction kettle again until a temperature of the reaction system reaches 90° C.˜130° C., and keeping the temperature at 90° C.˜130° C. for 20˜40 min to obtain said diacetyl tartaric acid esters of mono- and di-glycerides. The preparation method according to the present invention has advantages of simple process, low production cost, high yield, good product quality and environmental friendliness.
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