CAS: 30233-64-8; Monobehenin

该化合物是属于甘蓝酯类的化学化合物,产自甘蓝和苯酸,是一种长链脂肪酸,其典型特征为蜡质,通常用作乳胶,稳定剂和厚度剂,特别是在化妆品和制药业.甘蓝单体酸,因其有能力加强奶油和润滑剂的质质和稳定性,使其成为个人护理产品中有价值的成分.此外,它与广泛的其他成分具有良好的兼容性,有助于其配方的多用途.该化合物一般被视为安全用于化妆品和食品产品,尽管应当遵循具体的规范.其水恐性质允许其形成稳定的乳液,这对于保持预期的一致性和热液应用性至关重要.

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上下游产品

Docosanoic Acid 2,2-Dimethyl-[1,3]Dioxolan-4-Ylmethyl Ester 228263-82-9

合成工艺路线路线简述

    📜二十二酰氯置于吡啶体系中,用 甲醇,二氯甲烷 作为反应溶剂,化学反应 12.0H,反应生成 二十二烷酸甘油单酯
    参考文献:Synthesis Of Glycerolipids Containing Simple Linear Acyl Chains Or Aromatic Rings And Evaluation Of Their Mincle Signaling Activity
    标题:Synthesis Of Glycerolipids Containing Simple Linear Acyl Chains Or Aromatic Rings And Evaluation Of Their Mincle Signaling Activity
    摘要:合成的甘油酯衍生物具有简单的烷基链,可刺激与先天性免疫系统相关的 Mincle 介导的信号检测.
    DOI:10.1039/c8Cc07322H

    海关参考信息

    专利信息


    专利号:US-11717498-B2
    优先权日:2013-12-31
    标题 :Methods of treatment using amphetamine controlled release, prodrug, and abuse deterrent dosage forms
    发明人:POPP KARL; MECKLER HAROLD
    权利人:Chemapotheca LLC; PHARMAPOTHECA A INC
    摘要:The invention also relates to pharmaceutical compositions comprising highly pure amphetamine and amphetamine-class compounds resulting from the synthesis of chiral and racemic amphetamine derivatives by stereospecific, regioselective cuprate addition reaction with aziridine phosphoramidate compounds, and to methods of manufacturing, delivering, and using the amphetamine compounds resulting from the synthesis of chiral and racemic amphetamine derivatives by stereospecific, regioselective cuprate addition reaction with aziridine phosphoramidate compounds.

    专利号:US-12043612-B2
    优先权日:2020-05-09
    标 题 :Methods of manufacturing a bifunctional compound, ultrapure forms of the bifunctional compound, and dosage forms comprising the same
    发明人:ALLAN LAURA E N; CHEN CHUNGPIN HERMAN; DONG HANQING; GROSSO JOHN A; HASKELL III ROYAL J; LLOYD RHYS; REECE HAYLEY
    权利人:ARVINAS OPERATIONS INC
    摘要:The present disclosure relates to ultra-pure forms, polymorphs, amorphous forms, and formulations of N-[(1r,4r)-4-(3-chloro-4-cyanophenoxy)cyclohexyl]-6-[4-({4-[2-(2,6-dioxopiperidin-3-yl)-6-fluoro-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl]piperazin-1-yl}methyl)piperidin-1-yl]pyridazine-3-carboxamide, referred to herein as Compound A:The present disclosure also relates methods of manufacturing and purifying the same, as well as intermediates useful in the synthesis of Compound A. The ultra-pure forms, polymorphs, amorphous forms, and formulations of Compound A can be used as therapeutic agents for the treatment of various diseases and conditions such as cancer.

    专利号:US-2023114753-A1
    优先权日:2020-03-06
    标 题 :Use of a group of markers for diagnosing and adjusting treatment of primary biliary cholangitis, pharmaceutical composition and solid dosage form for treating primary biliary cholangitis
    发明人:JAIN NITIN
    权利人:MILI HEALTHCARE TRADE DMCC LLC
    摘要:A method of diagnosis and treatment of primary biliary cholangitis is provided. Additionally, a pharmaceutical composition and a solid dosage form for the treatment of primary biliary cholangitis, containing ursodeoxycholic and obeticholic acids, are provided. The technical contribution resides in obtaining a new all-purpose pharmaceutical composition and solid dosage form for the treatment of PBC, which includes both ursodeoxycholic and obeticholic acids, which is effective in use at all stages of PBC and has a complex mechanism of action. In particular, simultaneous blockage of the transport and synthesis of bile acids is achieved.

    专利号:US-12295961-B2
    优先权日:2009-12-31
    标 题:Modulation of solubility, stability, absorption, metabolism, and pharmacokinetic profile of lipophilic drugs by sterols
    发明人:DHINGRA OM
    权利人:MARIUS PHARMACEUTICALS INC
    摘要:A formulation for drug delivery, providing enhanced modulation of solubility, stability, absorption, metabolism, and/or pharmacokinetic profile of a lipophilic therapeutic agent by formulation with sterols and/or sterol esters, resulting in higher bioavailability of a therapeutic agent administered to a subject in need of such therapeutic agent. The formulation contains a therapeutic agent and a sterol or sterol ester, and can, optionally, further contain a solubilizer and/or an enhancing agent. Also described are pharmaceutical compositions containing the formulations and methods of making and methods of using the formulations and pharmaceutical compositions. Formulations of the disclosure can be constituted to minimize the synthesis of dihydrotestosterone when the therapeutic agent includes testosterone or testosterone esters.

    专利号:EP-2354120-A1
    优先权日:2003-08-20
    标题 :Synthesis of acyloxyalkyl carbamate prodrugs and intermediates thereof
    发明人:GALLOP MARK A; YAO FENMEI; LUDWIKOW MARIA J; PHAN THU; PENG GE
    权利人:XENOPORT INC
    摘要:The present invention relates to acyloxyalkyl carbamate prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof, pharmaceutical compositions thereof, methods of making prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof, methods of using prodrugs of (±)-4-amino-3-(4-tluorophenyl)butanoic acid and analogs thereof, and pharmaceutical compositions thereof for treating or preventing common diseases and/or disorders such as spasticity and/or acid reflux disease. The present invention also relates to acyloxyalkyl carbamate prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof which are suitable for oral administration and to sustained release oral dosage forms thereof.

    专利号:US-11850220-B2
    优先权日:2020-05-19
    标题 :Synthesis of ibuprofen hybrid conjugates as anti-inflammatory and analgesic agents
    发明人:PANDA SIVA
    权利人:UNIV RES INST INC AUGUSTA
    摘要:Disclosed herein as ibuprofen hybrid conjugates and methods of their use to reduce inflammation, pain, and fever. The ibuprofen conjugates have potent anti-inflammatory and analgesic properties with low potential for ulcerogenic activity. An exemplary compound is an ibuprofen-amino acid-4-aminophenol hybrid. Also disclosed are methods of treating or reducing inflammation, pain, and fever in a subject.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1208/s12249-012-9908-y
    摘要:Wavikar P, Vavia P. Nanolipidgel for Enhanced Skin Deposition and Improved Antifungal Activity. AAPS PharmSciTech. 2012 Dec 21;14(1):222–33. doi: 10.1208/s12249-012-9908-y.
    参考文献:10.1096/fasebj.11.1.9034165
    摘要:Ghosh S, Strum JC, Bell RM. Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45–50. doi: 10.1096/fasebj.11.1.9034165.
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