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1,2-Distearo-3-elaidin | 93452-42-7

中文名称
——
中文别名
——
英文名称
1,2-Distearo-3-elaidin
英文别名
1,2-Dioctadecanoyl-3-[cis-9-octadecenoyl]-rac-glycerol;[2-octadecanoyloxy-3-[(E)-octadec-9-enoyl]oxypropyl] octadecanoate
1,2-Distearo-3-elaidin化学式
CAS
93452-42-7
化学式
C57H108O6
mdl
——
分子量
889.481
InChiKey
YFFIQXNTTVSKJC-AZPGRJICSA-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

物化性质

  • 物理描述:
    Solid
  • 熔点:
    42.1°C

计算性质

  • 辛醇/水分配系数(LogP):
    24.3
  • 重原子数:
    63
  • 可旋转键数:
    55
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    78.9
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    硬脂酸吡啶草酰氯 作用下, 以 氯仿 为溶剂, 反应 76.0h, 生成 1,2-Distearo-3-elaidin
    参考文献:
    名称:
    含有桉树酸的混合二酸甘油三酸酯的合成及理化特性
    摘要:
    AbstractThe synthesis of symmetrical and asymmetrical palmito‐ and stearo‐elaidic triglycerides (PEP, SES, EPP, PEE, ESS, and SEE, in which P=palmitic, S=stearic, and E=elaidic acid) was undertaken to investigate their polymorphism. The chemical pathways and the purification steps, including crystallization and adsorption chromatography, are described. The different chromatographic analyses (gas‐liquid chromatography: carbon number profile and fatty acid methyl ester profile, and high‐performance liquid chromatography) revealed that the purity of the synthesized products was superior to 99% except for SES (>96%). The thermal behavior, as well as the polymorphism of these triglycerides, has been investigated by means of differential scanning calorimetry and powder X‐ray diffraction spectroscopy at variable temperatures. The six compounds crystallize according to a double chainlength packing. The most stable polymorphic form of palmito‐elaidic triglycerides belongs to the β′ variety, whereas the stearo‐elaidic triglycerides are β stable.
    DOI:
    10.1007/s11746-998-0043-6
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文献信息

  • Boemer; Kappeller, Fette und Seifen, 1937, vol. 44, p. 342
    作者:Boemer、Kappeller
    DOI:——
    日期:——
  • COCKMAN, SAMANTHA J.;JOLL, CYNTHIA A.;MORTIMER, BOK-CHENG;REDGRAVE, TREVO+, AUSTRAL. J. CHEM., 43,(1990) N2, C. 2093-2097
    作者:COCKMAN, SAMANTHA J.、JOLL, CYNTHIA A.、MORTIMER, BOK-CHENG、REDGRAVE, TREVO+
    DOI:——
    日期:——
  • Synthesis and physicochemical characterization of mixed diacid triglycerides that contain elaidic acid
    作者:P. Elisabettini、G. Lognay、A. Desmedt、C. Culot、N. Istasse、E. Deffense、F. Durant
    DOI:10.1007/s11746-998-0043-6
    日期:1998.2
    AbstractThe synthesis of symmetrical and asymmetrical palmito‐ and stearo‐elaidic triglycerides (PEP, SES, EPP, PEE, ESS, and SEE, in which P=palmitic, S=stearic, and E=elaidic acid) was undertaken to investigate their polymorphism. The chemical pathways and the purification steps, including crystallization and adsorption chromatography, are described. The different chromatographic analyses (gas‐liquid chromatography: carbon number profile and fatty acid methyl ester profile, and high‐performance liquid chromatography) revealed that the purity of the synthesized products was superior to 99% except for SES (>96%). The thermal behavior, as well as the polymorphism of these triglycerides, has been investigated by means of differential scanning calorimetry and powder X‐ray diffraction spectroscopy at variable temperatures. The six compounds crystallize according to a double chainlength packing. The most stable polymorphic form of palmito‐elaidic triglycerides belongs to the β′ variety, whereas the stearo‐elaidic triglycerides are β stable.
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