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testosterone-17-sulfate triethylammonium salt | 20997-99-3

中文名称
——
中文别名
——
英文名称
testosterone-17-sulfate triethylammonium salt
英文别名
Testosterone Sulfate Triethylamine Salt;N,N-diethylethanamine;[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] hydrogen sulfate
testosterone-17-sulfate triethylammonium salt化学式
CAS
20997-99-3
化学式
C6H15N*C19H28O5S
mdl
——
分子量
469.686
InChiKey
AGRILWRSYZNKSA-JZSNIJFVSA-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

  • 溶解度:
    氯仿(微溶)、乙醇、甲醇(微溶)

计算性质

  • 辛醇/水分配系数(LogP):
    5.05
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    92.3
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    睾酮三氧化硫-三乙胺复合物吡啶 作用下, 反应 2.0h, 以40%的产率得到testosterone-17-sulfate triethylammonium salt
    参考文献:
    名称:
    A simple method for the small scale synthesis and solid-phase extraction purification of steroid sulfates
    摘要:
    Steroid sulfates are a major class of steroid metabolite that are of growing importance in fields such as anti-doping analysis, the detection of residues in agricultural produce or medicine. Despite this, many steroid sulfate reference materials may have limited or no availability hampering the development of analytical methods. We report simple protocols for the rapid synthesis and purification of steroid sulfates that are suitable for adoption by analytical laboratories. Central to this approach is the use of solid-phase extraction (SPE) for purification, a technique routinely used for sample preparation in analytical laboratories around the world. The sulfate conjugates of sixteen steroid compounds encompassing a wide range of steroid substitution patterns and configurations are prepared, including the previously unreported sulfate conjugates of the designer steroids furazadrol (17 beta-hydroxyandrostan[2,3-d]isoxazole), isofurazadrol (17 beta-hydroxyandrostan[3,2-c]isoxazole) and trenazone (17 beta-hydroxyestra-4,9-dien-3-one). Structural characterization data, together with NMR and mass spectra are reported for all steroid sulfates, often for the first time. The scope of this approach for small scale synthesis is highlighted by the sulfation of 1 mu g of testosterone (17 beta-hydroxyandrost-4-en-3-one) as monitored by liquid chromatography-mass spectrometry (LCMS). (C) 2014 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2014.09.006
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文献信息

  • A simple method for the small scale synthesis and solid-phase extraction purification of steroid sulfates
    作者:Christopher C. Waller、Malcolm D. McLeod
    DOI:10.1016/j.steroids.2014.09.006
    日期:2014.12
    Steroid sulfates are a major class of steroid metabolite that are of growing importance in fields such as anti-doping analysis, the detection of residues in agricultural produce or medicine. Despite this, many steroid sulfate reference materials may have limited or no availability hampering the development of analytical methods. We report simple protocols for the rapid synthesis and purification of steroid sulfates that are suitable for adoption by analytical laboratories. Central to this approach is the use of solid-phase extraction (SPE) for purification, a technique routinely used for sample preparation in analytical laboratories around the world. The sulfate conjugates of sixteen steroid compounds encompassing a wide range of steroid substitution patterns and configurations are prepared, including the previously unreported sulfate conjugates of the designer steroids furazadrol (17 beta-hydroxyandrostan[2,3-d]isoxazole), isofurazadrol (17 beta-hydroxyandrostan[3,2-c]isoxazole) and trenazone (17 beta-hydroxyestra-4,9-dien-3-one). Structural characterization data, together with NMR and mass spectra are reported for all steroid sulfates, often for the first time. The scope of this approach for small scale synthesis is highlighted by the sulfation of 1 mu g of testosterone (17 beta-hydroxyandrost-4-en-3-one) as monitored by liquid chromatography-mass spectrometry (LCMS). (C) 2014 Elsevier Inc. All rights reserved.
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