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hexanedioic acid bis-pentylamide | 547751-03-1

中文名称
——
中文别名
——
英文名称
hexanedioic acid bis-pentylamide
英文别名
N,N'-dipentyl-adipamide;N,N'-Dipentyl-adipamid;Adipinsaeure-bis-pentylamid;N,N'-dipentylhexanediamide
hexanedioic acid bis-pentylamide化学式
CAS
547751-03-1
化学式
C16H32N2O2
mdl
——
分子量
284.442
InChiKey
HFQXHTXYNHDTOU-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

物化性质

  • 沸点:
    502.0±33.0 °C(Predicted)
  • 密度:
    0.934±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    20
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    hexanedioic acid bis-pentylamide 在 lithium aluminium tetrahydride 、 氧化亚氮 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 38.0h, 生成 (Z)-1-{N-pentyl-N-[6-(N-pentylammoniohexyl)amino]}diazen-1-ium-1,2-diolate
    参考文献:
    名称:
    More Lipophilic Dialkyldiamine-Based Diazeniumdiolates:  Synthesis, Characterization, and Application in Preparing Thromboresistant Nitric Oxide Release Polymeric Coatings
    摘要:
    The synthesis, characterization, and biomedical application in preparing more thromboresistant polymeric coatings for a series of lipophilic dialkyldiamine-based diazeniumdiolates are described. Dialkylhexamethylenediamine diazeniumdiolates of the form RN[N(O)NO](-)-(CH2)(6)(NH2R)-R-divided by, where R = CH3, CH2CH3, (CH2)(2)CH3, (CH2)(3)CH3, (CH2)(4)CH3, (CH2)(5)CH3, and (CH2)(11)CH3, are prepared via reaction of the corresponding diamine with NO. The more lipophilic diazeniumdiolates [e.g., R = (CH2)(3)CH3] can be incorporated into hydrophobic polymeric films (e.g., plasticized PVC), and the resulting materials release NO for extended periods of time upon exposure to PBS buffer. The mechanism of NO release from these films is examined in detail. More stable initial NO release can be achieved by adding lipophilic anionic species (e.g., tetraphenylborate derivative) to the polymeric material to buffer the activity of protons within the organic phase. It is shown that the use of these new lipophilic NO-donors in polymers provides the ability to tailor NO release rates for a variety of medical applications. As an example, polymers doped with N,N'-dibutylhexamethylenediamine diazeniumdiolate and a tetraphenylborate derivative are employed as coatings for vascular grafts in sheep. The NO release grafts exhibited enhanced performance and had an average 95% thrombus-free surface area compared to 42% for the corresponding control grafts when examined after 21d of implantation.
    DOI:
    10.1021/jm030286t
  • 作为产物:
    描述:
    1-氨基戊烷己二酰氯三乙胺 作用下, 以 氯仿 为溶剂, 反应 3.33h, 以71%的产率得到hexanedioic acid bis-pentylamide
    参考文献:
    名称:
    Use of additive sites to control nitric oxide release from nitric oxide donors contained within polymers
    摘要:
    一种增加、延长和/或控制聚合物材料中含有NO加合物的释放速率的方法。这种含有NO的聚合物材料可以在血液接触设备等设备中找到用途,并且利用相同的生物相容性设备。该方法和设备利用阴离子位添加剂、酸性位添加剂和/或产生酸性位添加剂在含有NO加合物的聚合物中产生更高通量的NO,超过NO阈值水平,以实现大幅预防和/或最小化诸如血小板活化或粘附等反应。
    公开号:
    US20060008529A1
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文献信息

  • Use of additive sites to control nitric oxide release from nitric oxide donors contained within polymers
    申请人:Meyerhoff E. Mark
    公开号:US20060008529A1
    公开(公告)日:2006-01-12
    A method for increasing, prolonging, and/or controlling the release rates of nitric oxide (NO) from polymeric materials containing NO adducts. Such NO-containing polymeric materials may find use in devices such as blood contacting devices, and biocompatible devices utilizing the same. The method and device utilizes anionic site additives, acidic site additives and/or acidic producing site additives in a polymer that contains NO-adducts to generate higher fluxes of NO to exceed NO threshold levels desirable to substantially prevent and/or minimize reactions such as platelet activation or adhesion.
    一种增加、延长和/或控制聚合物材料中含有NO加合物的释放速率的方法。这种含有NO的聚合物材料可以在血液接触设备等设备中找到用途,并且利用相同的生物相容性设备。该方法和设备利用阴离子位添加剂、酸性位添加剂和/或产生酸性位添加剂在含有NO加合物的聚合物中产生更高通量的NO,超过NO阈值水平,以实现大幅预防和/或最小化诸如血小板活化或粘附等反应。
  • Catalytic Hydrogenation of Amides to Amines
    作者:Bruno Wojcik、Homer Adkins
    DOI:10.1021/ja01326a061
    日期:1934.11
  • Paden; Adkins, Journal of the American Chemical Society, 1936, vol. 58, p. 2493
    作者:Paden、Adkins
    DOI:——
    日期:——
  • More Lipophilic Dialkyldiamine-Based Diazeniumdiolates:  Synthesis, Characterization, and Application in Preparing Thromboresistant Nitric Oxide Release Polymeric Coatings
    作者:Melissa M. Batchelor、Sylvie L. Reoma、Paul S. Fleser、Vijay K. Nuthakki、Rose E. Callahan、Charles J. Shanley、Jeffrey K. Politis、Jessica Elmore、Scott I. Merz、Mark E. Meyerhoff
    DOI:10.1021/jm030286t
    日期:2003.11.1
    The synthesis, characterization, and biomedical application in preparing more thromboresistant polymeric coatings for a series of lipophilic dialkyldiamine-based diazeniumdiolates are described. Dialkylhexamethylenediamine diazeniumdiolates of the form RN[N(O)NO](-)-(CH2)(6)(NH2R)-R-divided by, where R = CH3, CH2CH3, (CH2)(2)CH3, (CH2)(3)CH3, (CH2)(4)CH3, (CH2)(5)CH3, and (CH2)(11)CH3, are prepared via reaction of the corresponding diamine with NO. The more lipophilic diazeniumdiolates [e.g., R = (CH2)(3)CH3] can be incorporated into hydrophobic polymeric films (e.g., plasticized PVC), and the resulting materials release NO for extended periods of time upon exposure to PBS buffer. The mechanism of NO release from these films is examined in detail. More stable initial NO release can be achieved by adding lipophilic anionic species (e.g., tetraphenylborate derivative) to the polymeric material to buffer the activity of protons within the organic phase. It is shown that the use of these new lipophilic NO-donors in polymers provides the ability to tailor NO release rates for a variety of medical applications. As an example, polymers doped with N,N'-dibutylhexamethylenediamine diazeniumdiolate and a tetraphenylborate derivative are employed as coatings for vascular grafts in sheep. The NO release grafts exhibited enhanced performance and had an average 95% thrombus-free surface area compared to 42% for the corresponding control grafts when examined after 21d of implantation.
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