Français
2. Cardanol reactive sites
Cardanol is very difficult to obtain via conventional chemical synthesis routes, as the aliphatic side chain is in the meta position relative to the phenol group, which generally directs all substitutions to the ortho and/or para positions. Cardanol lends itself to a wide range of functionalizations leading to specific properties of interest for high value-added polymers. Structural modifications can be carried out on the hydroxyl group, on the aromatic ring and on the side chain (figure 3 ).
The Ultimate Scientific and Technical Reference
This article is included in
Plastics and composites
This offer includes:
Knowledge Base
Updated and enriched with articles validated by our scientific committees
Services
A set of exclusive tools to complement the resources
Practical Path
Operational and didactic, to guarantee the acquisition of transversal skills
Doc & Quiz
Interactive articles with quizzes, for constructive reading
Cardanol reactive sites
Cardanol applications in chemistry
Bibliography
Regulations
Directive no. 2000/60/EC of 10/23/00 establishing a framework for Community action in the field of water policy
Regulation (EC) no. 1907/2006 of 18/12/06 concerning the Registration, Evaluation, Authorization and Restriction of Chemicals (REACH), establishing a European Chemicals Agency
Patents
US20060142501, 2006. M. V. Badiger, P. P. Wadgaonkar, A. K. Lele, A. S. Shedge, D. Hourdet, P. Perrin and C. Chassenieux, Hydrophobically modified polyacrylic acid [PAA] and process of preparation thereof.
US 6255439, 2001. C. V. Avadhani, P. P. Wadgaonkar and S. Sivaram.
US2002142110A1, 2002. J. S. Mathew, S. P. Vernekar, R. Mercier and R. Kerboua, Novel polyimides, process for...
Directory
Manufacturers – Suppliers – Distributors (non-exhaustive list)
Cardolite Corporation (Corporate Headquarters), United States
Palmer International, United States
Senesel...
The Ultimate Scientific and Technical Reference
