Decyl α/β-D-Xylopyranoside

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: Decyl α/β-D-Xylopyranoside
• 英文别名: decyl D-xyloside；decyl D-xylopyranoside；n-decyl D-xyloside；(3R,4S,5R)-2-decoxyoxane-3,4,5-triol
• 化学式: C₁₅H₃₀O₅
• 分子量: 290.4
• InChiKey: MQBINCZBFIJILB-PEUVFPKISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  20
• 可旋转键数：
  10
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  79.2
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  丁二酸酐 、 Decyl α/β-D-Xylopyranoside 以 neat (no solvent) 为溶剂， 生成
  参考文献：
  名称：

  非离子表面活性剂的琥珀酰化：极性调节的理化特性，功能特性，生物降解性和数学建模

  摘要：

  含琥珀酸端基的阴离子表面活性剂是通过使用琥珀酸酐作为潜在的生物来源构造基团对非离子型表面活性剂进行琥珀酰化而合成的。设计了一种无溶剂和无催化剂的合成方法，用于琥珀酸酐与辛基，癸基和十二烷基聚木糖苷，二甘醇和四甘醇十二烷基醚以及单月桂酸甘油酯的单酯化反应。研究了由此获得的阴离子表面活性剂的理化和功能特性，并将其与非琥珀酰化的对应物进行了比较。在这些性质和通过添加亲水性琥珀酸部分引起的极性变化之间建立了相关性。还研究了琥珀酰化表面活性剂的生物降解性。最后，通过合意函数方法，

  DOI：

  10.1007/s11743-013-1489-6
• 作为产物：
  描述：

  D-吡喃木糖 、 硫酸二癸酯 在 sodium hydride 作用下， 以 various solvent(s) 为溶剂， 以65%的产率得到Decyl α/β-D-Xylopyranoside
  参考文献：
  名称：

  Klotz, Wolfgang; Schmidt, Richard R., Liebigs Annalen der Chemie, 1993, # 6, p. 683 - 690

  摘要：

  DOI：

文献信息

• ANTI-DANDRUFF SUGARS
  申请人：L'OREAL

  公开号：US20150250698A1

  公开（公告）日：2015-09-10

  The invention relates to the cosmetic use of at least one compounds according to the following formula (I), as an anti-dandruff agent or for preventing and/or treating scalp dandruff: where “sugar” denotes a monosaccharide residue chosen from rhamnose, xylose, fucose, mannose, lyxose, and arabinose; where R, substituting the anomeric oxygen in the sugar (represented by “O” in formula (I)), denotes a radical comprising 6 to 38 carbon atoms chosen from: —a linear or branched, saturated alkyl radical; —a linear or branched, alkenyl radical; said linear or branched saturated alkyl radical being optionally substituted by at least one OH and/or NH2 function; —if “sugar” denotes a mannose residue, R denotes a linear C6-C38 alkyl radical, substituted by at least one OH function or an NH2 function; and the salts and solvates and/or optical isomers thereof, alone or in a mixture, particularly racemic forms. The invention also relates to compounds according to formula (I), and cosmetic compositions containing same.

  本发明涉及至少一种根据以下公式（I）的化合物的化妆品用途，作为抗屑剂或用于预防/治疗头皮屑：其中“糖”表示一个单糖残基，选自鼠李糖、木糖、岩藻糖、甘露糖、来苏糖和阿拉伯糖；其中R代表糖（由公式（I）中的“O”表示）的异构氧上的一个基团，该基团包含6至38个碳原子，选自以下几种：—线性或支链的饱和烷基；—线性或支链的烯丙基；所述的线性或支链的饱和烷基可选择性地被至少一个OH和/或NH2功能基团取代；—如果“糖”表示一个甘露糖残基，R表示一个线性的C6-C38烷基，被至少一个OH功能或NH2功能取代；以及所述化合物的盐、溶剂化物和/或光学异构体，单独或混合使用，尤其是外消旋形式。本发明还涉及根据公式（I）的化合物，以及含有该化合物的化妆品组合物。
• US9833397B2
  申请人：——

  公开号：US9833397B2

  公开（公告）日：2017-12-05
• [EN] ANTI-DANDRUFF SUGARS<br/>[FR] SUCRES ANTIPELLICULAIRES
  申请人：OREAL

  公开号：WO2014044779A2

  公开（公告）日：2014-03-27

  The invention relates to the cosmetic use of at least one compounds according to the following formula (I), as an anti-dandruff agent or for preventing and/or treating scalp dandruff: where "sugar" denotes a monosaccharide residue chosen from rhamnose, xylose, fucose, mannose, lyxose, and arabinose; where R, substituting the anomeric oxygen in the sugar (represented by "O" in formula (I)), denotes a radical comprising 6 to 38 carbon atoms chosen from: - a linear or branched, saturated alkyl radical; - a linear or branched, alkenyl radical; said linear or branched saturated alkyl radical being optionally substituted by at least one OH and/or NH2 function; - if "sugar" denotes a mannose residue, R denotes a linear C6-C38 alkyl radical, substituted by at least one OH function or an NH2 function; and the salts and solvates and/or optical isomers thereof, alone or in a mixture, particularly racemic forms. The invention also relates to compounds according to formula (I), and cosmetic compositions containing same.
• Succinylation of Non-ionic Surfactants: Physicochemical Characterization, Functional Properties, Biodegradability and Mathematical Modeling of the Polarity Tuning
  作者：Mickaël Agach、Laurianne Moity、Benjamin Renault、Sinisa Marinkovic、Boris Estrine、Véronique Nardello-Rataj

  DOI：10.1007/s11743-013-1489-6

  日期：2014.7

  physicochemical and functional properties of anionic surfactants thus obtained were studied and compared with their non‐succinylated counterparts. A correlation between these properties and the polarity changes induced by the addition of the hydrophilic succinic acid moiety was established. The biodegradability of the succinylated surfactants has also been investigated. Finally, through a desirability

  含琥珀酸端基的阴离子表面活性剂是通过使用琥珀酸酐作为潜在的生物来源构造基团对非离子型表面活性剂进行琥珀酰化而合成的。设计了一种无溶剂和无催化剂的合成方法，用于琥珀酸酐与辛基，癸基和十二烷基聚木糖苷，二甘醇和四甘醇十二烷基醚以及单月桂酸甘油酯的单酯化反应。研究了由此获得的阴离子表面活性剂的理化和功能特性，并将其与非琥珀酰化的对应物进行了比较。在这些性质和通过添加亲水性琥珀酸部分引起的极性变化之间建立了相关性。还研究了琥珀酰化表面活性剂的生物降解性。最后，通过合意函数方法，
• Klotz, Wolfgang; Schmidt, Richard R., Liebigs Annalen der Chemie, 1993, # 6, p. 683 - 690
  作者：Klotz, Wolfgang、Schmidt, Richard R.

  DOI：——

  日期：——