CAS: 585-29-5; Triethylamine Formate

该化合物是挥发性缓冲盐,通常用于液色谱-质谱仪(LC-MS)的应用,因为它与电喷射电离子化兼容性(ESI),其分子量低,挥发程度高,尽量减少离子抑制,提高敏感度和分析分解中的最高分辨率,该化合物是反向相和水益互动液相色谱法(HILIC)的有效移动阶段添加剂,为极地和离子解解解液解析物提供更好的峰值形状.三乙胺供囚犯使用的三乙酰胺还显示水和有机溶剂的溶性良好,有助于方法的开发,其缓冲能力在pH3.5附近使其适合酸性条件,而其最小的残留能减少仪器污染.

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CAS号64-18-6 甲酸 | CAS号121-44-8 三乙胺

合成工艺路线路线简述

    📜二氧化碳,三乙胺置于氢气体系中,用 水 作为反应溶剂,化学反应生成 甲酸:三乙胺 1:1
    参考文献:Carbon Dioxide Mediated,Reversible Chemical Hydrogen Storage Using A Pd Nanocatalyst Supported On Mesoporous Graphitic Carbon Nitride
    标题:Carbon Dioxide Mediated,Reversible Chemical Hydrogen Storage Using A Pd Nanocatalyst Supported On Mesoporous Graphitic Carbon Nitride
    摘要:可逆的二氧化碳介导的化学氢存储首次使用负载在中孔石墨相氮化碳(pd/mpg-C3N4)上的异质pd催化剂进行示范.研究发现,Pd纳米颗粒均匀分散在mpg-C3N4上,平均尺寸为1.7纳米,且没有任何团聚现象.其在常温下对甲酸的脱氢反应表现出极佳的活性,周转频率达到144 H−1,甚至在没有外部碱的情况下亦然.初步的dft研究表明,Mpg-C3N4载体上的碱性位点在无表面活性剂的情况下,对稳定还原态的pd纳米颗粒以及通过去质子化甲酸来启动氢气释放起到协同作用.这些潜在相互作用通过x射线吸收近边结构(xanes)得到了进一步确认.除了脱氢反应外,Pd/mpg-C3N4还证明能够催化通过co2氢化再生甲酸.进一步阐明了co2氢化的主要影响因素,以提高所需甲酸的产量和选择性.
    DOI:10.1039/c4Ta01133C

    海关参考信息

    专利信息


    专利号:US-2012215002-A1
    优先权日:2009-10-09
    标 题:Synthesis of optically active intermediate for the preparation of montelukast
    发明人:LEFORT LAURENT
    权利人:LEFORT LAURENT
    摘要:The present invention relates to the synthesis of optically active alcohols by means of enantioselective hydrogenation of ketones in biphasic systems. In particular the present invention relates to the synthesis of an optically active alcohol of general formula (1).

    专利号:US-2011245503-A1
    优先权日:2008-11-28
    标题 :Enantioselective synthesis of asymmetric beta-carboline intermediates
    发明人:SANTOS LEONARDO; ESPINOZA MORAGA MARLENE; SHANKARAJAH NAGULA
    权利人:UNIV TALCA
    摘要:Described herein is a new asymmetric synthesis of imines to obtain β-carboline derivatives useful as key intermediate compounds for the synthesis of phosphodiesterase inhibitors using a new process with palladium or ruthenium hydride and/or nickel boride to reduce chiral intermediates. The use of chloroformate chiral auxiliaries is further described for the reduction and asymmetric hydrogenation of imines to obtain β-carboline derivatives and intermediate compounds used in the preparation thereof.

    专利号:WO-2024259491-A1
    优先权日:2023-06-23
    标 题:New synthesis method
    发明人:FORD DANIEL; POZNAKS VIKTORS; FOTINS JURIS; ÄŒERÅ…AKS DMITRIJS
    权利人:THE HEART RES INSTITUTE LTD
    摘要:The present disclosure generally relates to a process for the synthesis of AZD6482. In particular, the present disclosure also relates to a process for the synthesis of enantiomerically pure AZD6482. The present disclosure also relates to a process for the synthesis of enantiomerically pure intermediates. The present disclosure also relates to compounds prepared by the processes and the use of such compounds to prepare compositions and to treat disorders.

    专利号:US-9303056-B2
    优先权日:2012-07-25
    标题 :Monomer for synthesis of RNA, method for producing same, and method for producing RNA
    发明人:KATAOKA MASANORI
    权利人:UNIV KOCHI
    摘要:The objective of the present invention is to provide a monomer for RNA synthesis which can be efficiently produced and therefore by which the producing cost of RNA can be remarkably decreased, and a method for efficiently producing the monomer in a small number of steps. In addition, the objective of the present invention is also to provide a method by which RNA can be efficiently produced even when a approximately stoichiometry amount of the monomer for RNA synthesis is used. The monomer for RNA synthesis according to the present invention is represented by the following formula (I) or (I′): n nwherein R 1 is a protective group of the hydroxy group and R 2 is an alkyl group or the like.

    专利号:US-9856251-B2
    优先权日:2008-09-03
    标题:Substituted berbines and processes for their synthesis
    发明人:WANG PETER X; MOSER FRANK W; CANTRELL GARY L; GROTE CHRISTOPHER W
    权利人:MALLINCKRODT LLC
    摘要:The present invention provides processes for the synthesis of substituted berbine compounds. Also provided are intermediates used in the synthesis of substituted berbine compounds.

    专利号:US-2025019350-A1
    优先权日:2023-06-16
    标题 :Synthesis of the prostate specific membrane antigen (psma) radiolabeled inhibitor [18f]dcfpyl
    发明人:BENITES PEDRO; ROBINSON SIMON P; SIEGLER ROBERT W
    权利人:PROGENICS PHARM INC
    摘要:Provided herein are methods and related compositions, including kits, for the improved synthesis, preparation and/or storage of [18F]DCFPyL. Also provided are methods of using [18F]DCFPyL, such as for imaging.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: J S Wang, Et Al. Protective Alterations In Phase 1 And 2 Metabolism Of Aflatoxin B1 By Oltipraz In Residents Of Qidong, People'S Republic Of China. J Natl Cancer Inst. 1999 Feb 17;91(4):347-54.

    合成参考文献


    摘要:Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 402.
    参考文献:10.1007/bf01197834
    摘要:Wieser H, Belitz HD. Isolation and enzymatic fragmentation of the coeliac-active gliadin peptide CT-1. Z Lebensm Unters Forsch. 1992 Jul;195(1):22–6. doi: 10.1007/bf01197834.
    参考文献:10.1007/bf01198412
    摘要:Wieser H, Belitz HD. Coeliac active peptides from gliadin: large-scale preparation and characterization. Z Lebensm Unters Forsch. 1992 Mar;194(3):229–34. doi: 10.1007/bf01198412.
    参考文献:10.1007/bf00966225
    摘要:Elrod K, Okamoto H, Greenbaum LM, Buccafusco JJ. Inactivation of kallikrein and kininases and stabilization of whole rat brain kinin levels following focused microwave irradiation. Neurochem Res. 1986 Oct;11(10):1463–71. doi: 10.1007/bf00966225.
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