133117-08-5

Basic information

• Product Name: 3-cyano-3,5,5-trimethyl cyclohexylimine
• Synonyms: 3-cyano-3,5,5-trimethyl cyclohexylimine
• CAS NO: 133117-08-5
• Molecular Weight: 166.266
• Mol File: 133117-08-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3-cyano-3,5,5-trimethyl cyclohexylimine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-cyano-3,5,5-trimethyl cyclohexylimine(133117-08-5)
• EPA Substance Registry System: 3-cyano-3,5,5-trimethyl cyclohexylimine(133117-08-5)

Safety Data

• Hazardous Substances Data: 133117-08-5(Hazardous Substances Data)

Upstream product

• 78-59-1 3,5,5-Trimethylcyclohex-2-en-1-one 
• 79848-85-4 3-cyano-3,5,5-trimethylcyclohexaneimine 
• 7027-11-4 isophoronenitrile 

Relevant articles and documents

Method for preparing IPDI (isophorone diisocyanate)

The invention discloses a method for preparing IPDI (isophorone diisocyanate). The method comprises the following steps: (1) isophorone and hydrogen cyanide are subjected to a reaction in the presenceof a catalyst to obtain isophorone nitrile; (2) isophorone nitrile obtained in step (1), ammonia and hydrogen are subjected to a reaction in the presence of a catalyst to obtain isophorone diamine; (3) isophorone diamine is subjected to a phosgenation reaction to obtain IPDI, wherein the content of impurities containing secondary amine groups in isophorone diamine subjected to the phosgenation reaction in step (3) is smaller than or equal to 0.5wt%, preferably smaller than or equal to 0.3wt%, and more preferably smaller than or equal to 0.1wt%. By means of the method, content of hydrolyzed chlorine in the IPDI product can be effectively reduced, the yellowing resistance of the product is effectively improved, and the harm that downstream products are unqualified due to existence of hydrolyzed chlorine in the product is reduced.

Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation

Heterocyclic aromatic amides having a hydroxy group adjacent to the amide functionality are useful as antifungal agents, particularly for plants.

3-AMINOMETHYL-3, 5, 5-TRIMETHYL CYCLOHEXYLAMINE PREPARATION METHOD

Provided is a 3-aminomethyl-3,5,5-trimethylcyclohexylamine preparation method. A feeding flow of 3-cyano-3,5,5-trimethylcyclohexylimine is reacted with NH3 and hydrogen in the presence of a hydrogenation catalyst; the method is characterized by: firstly adding a basic compound to the feeding flow of 3-cyano-3,5,5-trimethylcyclohexylimine, and then after a portion of 3-cyano-3,5,5-trimethylcyclohexylimine has reacted, adding an acidic compound to reaction materials for further hydrogenation reaction to prepare the product. The method ensures that the aminonitrile content in the product is low, thus effectively reducing the duration of the reaction and greatly reducing the consumption of the catalyst during the hydrogenation reaction process.