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N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniopentanoate | 145441-34-5

中文名称
——
中文别名
——
英文名称
N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniopentanoate
英文别名
N,N-Dimethyl-N-(3-F-octylpropyl)-5-ammoniopentanoate;5-[4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl(dimethyl)azaniumyl]pentanoate
N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniopentanoate化学式
CAS
145441-34-5
化学式
C18H20F17NO2
mdl
——
分子量
605.335
InChiKey
WKKDKWOQDJGHBD-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):
    7.7
  • 重原子数:
    38
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    40.1
  • 氢给体数:
    0
  • 氢受体数:
    19

SDS

SDS:c67701ca374cfa5f6676f1208a4a324e
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反应信息

  • 作为产物:
    描述:
    2-氨基甲苯-5-磺酸 在 lithium aluminium tetrahydride 、 氯化亚砜 、 Amberlite (OH- form) 作用下, 以 乙醚 为溶剂, 反应 50.0h, 生成 N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniopentanoate
    参考文献:
    名称:
    Synthesis and bioacceptability of fluorinated surfactants derived from F-alkylated tertiary amines
    摘要:
    Two methods for synthesizing tertiary F-alkylated amines are reported. The more general method allows the access in 56-87% yields to various NN-dialkyl F-alkyl amines. These amines are key intermediates leading in 52-96% yields to several families of surfactants, including zwitterionic and cationic derivatives and amine oxides, potentially useful in the formulation of fluorocarbon emulsions for diagnostic and therapeutic uses. The toxicity of the new surfactants and the influence of the polar head were assessed: the long chain compounds (8, 9 and 10) were found to be toxic for cell cultures and the zwitterionic compounds (7b and 8) have a LD50 < 250 mg.kg bw-1 in mice. The hemolysis test highlights the influence of the polar head: the zwitterionic compounds (7 and 8) were found to be non-hemolytic even at remarkably high concentrations (100 g l-1 for 8), whereas the cationic compounds 9 are highly hemolytic even at very low concentrations (0.05 g l-1).
    DOI:
    10.1016/0223-5234(92)90020-2
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文献信息

  • Synthesis and bioacceptability of fluorinated surfactants derived from F-alkylated tertiary amines
    作者:JB Nivet、R Bernelin、M Le Blanc、JG Riess
    DOI:10.1016/0223-5234(92)90020-2
    日期:1992.12
    Two methods for synthesizing tertiary F-alkylated amines are reported. The more general method allows the access in 56-87% yields to various NN-dialkyl F-alkyl amines. These amines are key intermediates leading in 52-96% yields to several families of surfactants, including zwitterionic and cationic derivatives and amine oxides, potentially useful in the formulation of fluorocarbon emulsions for diagnostic and therapeutic uses. The toxicity of the new surfactants and the influence of the polar head were assessed: the long chain compounds (8, 9 and 10) were found to be toxic for cell cultures and the zwitterionic compounds (7b and 8) have a LD50 < 250 mg.kg bw-1 in mice. The hemolysis test highlights the influence of the polar head: the zwitterionic compounds (7 and 8) were found to be non-hemolytic even at remarkably high concentrations (100 g l-1 for 8), whereas the cationic compounds 9 are highly hemolytic even at very low concentrations (0.05 g l-1).
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