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麦替卡因 | 7712-50-7

中文名称
麦替卡因
中文别名
桃金娘卡因麦替卡因;桃金娘卡因;马太卡因
英文名称
2-<2-(2-Diethylamino-ethoxy)-ethyl>-6,6-dimethyl-norpin-2-en = 1-Diethylamino-2-homomyrtenyl-ethan
英文别名
2-Homomyrtenyloxy-1-diethylaminoethan;2-Homomyrtenyloxy-1-diethylaminomethan;Myrtecaine;2-[2-(6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl)ethoxy]-N,N-diethylethanamine
麦替卡因化学式
CAS
7712-50-7
化学式
C17H31NO
mdl
——
分子量
265.439
InChiKey
BZRYYBWNOUALTQ-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

  • 熔点:
    <25 °C
  • 沸点:
    bp2-3 135-140°
  • 密度:
    0.930±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    12.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:eff1e6cab1f6026c08bcf7740cc745c0
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文献信息

  • [EN] DERMAL COMPOSITIONS CONTAINING UNNATURAL HYGROSCOPIC AMINO ACIDS<br/>[FR] COMPOSITIONS DERMATOLOGIQUES CONTENANT DES AMINOACIDES HYGROSCOPIQUES NON NATURELS
    申请人:MEDPHARM LTD
    公开号:WO2014072747A1
    公开(公告)日:2014-05-15
    Unnatural, hygroscopic amino acids are useful to enhance the moisture retention and uptake properties of skin. In particular, such amino acids are N-hydroxyserine, N- hydroxyglycine, L-homoserine,alpha-hydroxyglycine, 2-(aminooxy) -2-hydroxyacetic acid, 2-hydroxy-2-(hydroxyamino) acetic acid, 2- (aininooxy)acetic acid, and combinations thereof.
    不自然的、亲水性的氨基酸对增强皮肤的保湿和吸湿性能是有用的。特别是,这些氨基酸包括N-羟基丝氨酸、N-羟基甘氨酸、L-同丝氨酸、α-羟基甘氨酸、2-(氨氧基)-2-羟基乙酸、2-羟基-2-(羟氨基)乙酸、2-(氨氧基)乙酸,以及它们的组合。
  • Crosslinked hyaluronic acid compositions for tissue augmentation
    申请人:Sadozai K. Khalid
    公开号:US20050136122A1
    公开(公告)日:2005-06-23
    A hyaluronic acid (HA) composition includes crosslinked, water-insoluble, hydrated HA gel particles. The HA includes crosslinks represented by the following structural formula: HA—U—R 2 —U—HA The variables are defined herein. A method of augmenting tissue in a subject includes inserting a needle into a subject at a location in the subject that is in need of tissue augmentation, wherein the needle is coupled to a syringe loaded with the HA composition, and applying force to the syringe, to deliver the HA composition into the subject. A method of preparing the HA composition, includes forming water-insoluble, dehydrated crosslinked HA particles, separating the water-insoluble, dehydrated particles by average diameter, selecting a subset of particles by average diameter, and hydrating the subset of dehydrated particles with a physiologically compatible aqueous solution. Another method of preparing the crosslinked HA composition includes crosslinking a precursor of the crosslinked HA with a biscarbodiimide in the presence of a pH buffer and dehydrating the crosslinked HA. Also included is a method of augmenting tissue in a subject that is in need of tissue augmentation. A method of stabilizing crosslinked HA includes hydrating water-insoluble, dehydrated crosslinked HA with a physiologically compatible aqueous solution that includes a local anesthetic, wherein the value of storage modulus G′ for the stabilized composition is at least about 110% of the value of G′ for a non-stabilized composition,. Also included is the stabilized HA composition.
    一种透明质酸(HA)组合物包括交联的、不溶于水的、水合的HA凝胶颗粒。HA包括由以下结构式表示的交联:HA—U—R2—U—HA。变量在此定义。一种在受试者中增强组织的方法包括将针插入受试者体内需要组织增强的位置,其中针连接到装有HA组合物的注射器,并施加力量到注射器,将HA组合物注入受试者体内。一种制备HA组合物的方法包括形成不溶于水的、脱水的交联HA颗粒,通过平均直径分离不溶于水的、脱水的颗粒,通过平均直径选择颗粒的子集,并用生理兼容的水溶液使脱水的颗粒子集水化。另一种制备交联HA组合物的方法包括在pH缓冲剂存在下用双异氰酸酯交联交联HA的前体,并脱水交联HA。还包括一种在需要组织增强的受试者中增强组织的方法。一种稳定交联HA的方法包括用含有局部麻醉剂的生理兼容水溶液水化不溶于水的、脱水的交联HA,其中稳定组合物的存储模量G′的值至少为非稳定组合物G′值的约110%。还包括稳定的HA组合物。
  • Technology for the Preparation of Microparticles
    申请人:Malakhov Michael
    公开号:US20090098207A1
    公开(公告)日:2009-04-16
    Microspheres are produced by contacting a solution of a macromolecule or small molecule in a solvent with an antisolvent and a counterion, and chilling the solution. The microspheres are useful for preparing pharmaceuticals, nutraceuticals, cosmetic products and the like of defined dimensions.
    微球是通过将溶液中的大分子或小分子与抗溶剂和对离子接触,并冷却溶液而制备的。这些微球可用于制备具有明确定义尺寸的药物、营养保健品、化妆品等产品。
  • Analgesics, anaesthetics, antifoulants, aversants, irritants, incapacitants and compositions containing the same
    申请人:Blum Mel
    公开号:US20070225515A1
    公开(公告)日:2007-09-27
    Compounds and compositions the same. Method of making the compounds. The compounds and/or compositions used as an analgesic, anaesthetic, antifoulant, aversant, irritant, sternutator, neurodegenerator, counter irritant (delayed), rubifaciant, stomachic, fungicide, insecticide, preservative, circulatory stimulant, cardio-protective agent, immune booster, decongestant, anti-inflammatory agent, incapacitant, biocide, mildewcide, pharmaceutical, repellent, flavorant, carminative, antismoking agent, and/or antithrombotic agent. One of the compounds being lidocaine nonivamide. The compositions comprising one or more of: the compounds, one or more of an antioxidant, a UV absorber, and one or more biocides such as, for example, OBPA.
    化合物和组合物相同。制备这些化合物的方法。这些化合物和/或组合物用作止痛剂、麻醉剂、防污剂、驱避剂、刺激剂、喷鼻剂、神经变性剂、延迟性刺激剂、红斑剂、胃药、杀真菌剂、杀虫剂、防腐剂、循环刺激剂、心脏保护剂、免疫增强剂、通窍剂、抗炎剂、致残剂、生物杀灭剂、霉菌杀灭剂、药用、驱虫剂、调味剂、驱风剂、抗吸烟剂和/或抗血栓剂。其中一种化合物是利多卡因辛烷酸酯。组合物包括:这些化合物中的一种或多种、一种或多种抗氧化剂、一种或多种紫外线吸收剂,以及一种或多种生物杀灭剂,例如OBPA。
  • Odorless formulation for treating mucosal discontinuities
    申请人:——
    公开号:US20040132810A1
    公开(公告)日:2004-07-08
    The present invention includes a method for making a formulation for treating mucosal discontinuities, comprising: providing phenolic compounds and treating the purified phenolic compounds with sulfuric acid to make sulfonic acids and sulfonate salts. The present invention also includes formulations prepared by the method.
    本发明涉及一种用于制备治疗黏膜不连续的配方的方法,包括:提供酚类化合物,并用硫酸处理纯化的酚类化合物以制备磺酸和磺酸盐。本发明还包括通过该方法制备的配方。
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