N~1~-(5-Methylhexan-2-yl)-N~4~-(4-methylpentan-2-yl)benzene-1,4-diamine | 58446-49-4

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N~1~-(5-Methylhexan-2-yl)-N~4~-(4-methylpentan-2-yl)benzene-1,4-diamine
• 英文别名: 1-N-(5-methylhexan-2-yl)-4-N-(4-methylpentan-2-yl)benzene-1,4-diamine
• CAS: 58446-49-4
• 化学式: C₁₉H₃₄N₂
• 分子量: 290.5
• InChiKey: DYFAHIPGXPYHON-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  21
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  24.1
• 氢给体数：
  2
• 氢受体数：
  2

文献信息

• Process for producing paraphenylenediamine mixtures
  申请人：MONSANTO COMPANY

  公开号：EP0084527A2

  公开（公告）日：1983-07-27

  Mixtures of N,N'-disubstituted paraphenylenediamines are produced in a process wherein a nitrogen-containing compound such as 4-nitrodiphenylamine is reductively alkylated with a plurality of ketones in sequence.

  N,N'-二取代对苯二胺混合物的生产工艺是将含氮化合物（如 4-硝基二苯胺）与多个酮依次进行还原烷基化。
• PRIMER COMPOSITIONS FOR ADHESIVE BONDING SYSTEMS
  申请人：Henkel Corporation

  公开号：EP1902106B1

  公开（公告）日：2014-08-20
• PRIMER COMPOSITIONS FOR ADHESIVE BONDING SYSTEMS AND COATINGS
  申请人：Henkel AG & Co. KGaA

  公开号：EP2190900A2

  公开（公告）日：2010-06-02
• Cure accelerators for anaerobic adhesive compositions
  申请人：LOCTITE CORPORATION

  公开号：US20030207126A1

  公开（公告）日：2003-11-06

  The present invention provides a new class of materials effective as accelerators for curing anaerobic adhesives. The addition of these materials into anaerobic adhesives as a replacement for conventional curatives, such as APH and/or toluidines, surprisingly provides at least comparable cure speeds and physical properties for the reaction products formed therefrom.
• Primer Compositions for Adhesive Bonding Systems
  申请人：Roth Marcel

  公开号：US20100151253A1

  公开（公告）日：2010-06-17

  The present invention relates to primer compositions for adhesive bonding systems. The primer compositions may be in the form of sprayable aqueous dispersions, which are shelf stable at ambient temperatures for up to three months under ambient temperature conditions, and demonstrate a cure profile of 45 to 120 minutes within the temperature range of 220° F. to 350° F. within 60 minutes of application. Significantly, the inventive primer compositions are substantially free of chromate.