CAS: 19327-39-0; 3,6,9,12-Tetraoxaicosan-1-Ol

该化合物是一个合成化合物,其长链结构特征为多醚联系,分子由四醚(欧元)群体相互穿透的线性碳链组成,有助于其独特的特性.在链的一端存在氢氧(Euroxyl)功能组,增强了其在极地溶剂中的溶解性,并传播了水益特性.该化合物通常用于各种用途,包括由于其能够减少表面紧张度,在配方中作为表面活性剂或乳化剂使用.其结构允许与生物膜的灵活性和潜在互动,使其具有生物化学研究的兴趣.此外,四氧基结构还表明其潜在的稳定性和抗降解能力,在某些工业应用中是有利的.

结构式图片

相似化合物

3055-99-0 5274-63-5 618113-48-7

欧盟法规

[ECHA物质

上下游产品

CAS号112-60-7 三缩四乙二醇 | CAS号111-83-1 1-溴代正辛烷 | CAS号1351016-13-1 (E)-3,6,9,12-te... | CAS号75-21-8 环氧乙烷 | CAS号111-87-5 正辛醇 | CAS号19327-37-8 2-[2-(2-乙基己氧基)乙氧基]乙醇 | CAS号19327-38-9 三乙烯乙二醇辛酯 | CAS号19327-40-3 正辛基戊氧基乙烯炔 | CAS号4440-54-4 乳化剂 OPE-6,乳化剂 OP-6 | CAS号28115-75-5 POLYOXYETHYLENE...

合成工艺路线路线简述

    2-[2-(2-乙基己氧基)乙氧基]乙醇置于boron Trifluoride Diacetate体系中,化学反应生成四聚乙二醇单辛醚
    参考文献:Chakhovskoy Et Al.,Bulletin Des Societes Chimiques Belges,1956,Vol. 65,P. 453,470
    标题:Chakhovskoy Et Al.,Bulletin Des Societes Chimiques Belges,1956,Vol. 65,P. 453,470

    海关参考信息

    专利信息


    专利号:US-6217901-B1
    优先权日:1999-05-25
    标题:Liposome-assisted synthesis of polymeric nanoparticles
    发明人:PERROTT MICHAEL G; BARRY STEPHEN E
    权利人:ALNIS LLC
    摘要:Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs range in size from about 20 to about 1000 nm. The SPCs have surfaces that are complementary to surface sites of target molecules, resulting in the ability of the SPCs to selectively bind to molecular targets. The molecular recognition capability of these particles enables their use in diagnostic, therapeutic, and separation applications. The SPC is formed by contacting a target template molecule with a set of building blocks solubilized in the interior of a liposome, which building blocks are then polymerized into a network to form the synthetic polymer complement in the interior of the liposome. The target templates are removed to produce complementary sites in a SPC that map the surface of the target, resulting in a water-soluble SPC nanoparticle of similar dimensions as the interior of the liposome that originally supported it and capable of molecular recognition.

    专利号:US-2010055187-A1
    优先权日:2008-08-28
    标题:Nanovitamin synthesis
    发明人:AHN DONG JUNE
    权利人:AHN DONG JUNE
    摘要:Stable nanoparticulate vitamin compositions are prepared from agglomerated or larger sized vitamin particles of at least one vitamin compound by breaking down and/or solubilizing the agglomerated or larger sized vitamin particles and associating the particles with a surface modifying agent.

    专利号:US-2004058006-A1
    优先权日:1997-10-14
    标 题 :High affinity nanoparticles
    发明人:BARRY STEPHEN E; SOANE DAVID S
    权利人:ALNIS BIOSCIENCES INC
    摘要:High affinity nanoparticles are provided, as well as methods for their synthesis and use. The nanoparticles of the invention comprise high affinity molecules incorporated in a polymeric nanoparticle. The high affinity nanoparticles range in size from about 1 to about 1000 nm. The high affinity molecules of the nanoparticle have moieties that have high affinity for target molecules, resulting in the ability of the high affinity nanoparticle to selectively non-covalently bind to molecular targets. The molecular recognition capability of these particles enables their use in research, diagnostic, therapeutic, and separation applications. The nanoparticles of the invention may be formed by contacting target template molecules with a set of building blocks (which includes the high affinity molecule as one subset of the building block set), which are then polymerized into a network. Removal of the templates yields a polymeric nanoparticle with three-dimensional binding sites that are complementary in shape to at least a portion of the target and including high affinity molecules chemically anchored on the surfaces of the binding sites. The high affinity nanoparticle is then capable of molecular recognition and selective binding to target molecules when presented with the target molecule in a mixture of molecules.
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    主要参考文献

    参考标题:Highly Efficient Synthesis Of Monodisperse Poly(Ethylene Glycols) And Derivatives Through Macrocyclization Of Oligo(Ethylene Glycols)
    作者:Hua Zhang,Xuefei Li,Qiuyan Shi,Yu Li,Guiquan Xia,Long Chen,Zhigang Yang,Zhong-Xing Jiang |发布日期:2015.3.16
    摘要:A Macrocyclic Sulfate (Mcs)‐based Approach To Monodisperse Poly(Ethylene Glycols) (M‐pegs) And Their Monofunctionalized Derivatives Has Been Developed. Macrocyclization Of Oligo(Ethylene Glycols) (Oegs) Provides Mcs (Up To A 62‐membered Macrocycle) As Versatile Precursors For A Range Of Monofunctionalized M‐pegs. Through Iterative Nucleophilic Ring‐opening Reactions Of Mcs Without Performing Group

    合成参考文献


    参考文献:10.1073/pnas.1104984108
    摘要:Whitney JC, Hay ID, Li C, Eckford PDW, Robinson H, Amaya MF, Wood LF, Ohman DE, Bear CE, Rehm BH, Lynne Howell P. Structural basis for alginate secretion across the bacterial outer membrane. Proc. Natl. Acad. Sci. U.S.A. 2011 Jul 21;108(32):13083–8. doi: 10.1073/pnas.1104984108.
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