20701-67-1Relevant articles and documents
Novel long chain unsaturated diisocyanate from fatty acid: Synthesis, characterization, and application in bio-based polyurethane
Hojabri, Leila,Kong, Xiaohua,Narine, Suresh S.
, p. 3302 - 3310 (2010)
A novel long chain linear unsaturated terminal diisocyanate, 1,16-diisocyanatohexadec-8-ene (HDEDI) was synthesized from oleic acid via Curtius rearrangement. Its chemical structure was identified by FTIR, 1H NMR, 13C NMR, and HRMS. This diisocyanate was used as a starting material for the preparation of entirely bio-based polyurethanes (PUs) by reacting it with canola diol and canola polyol, respectively. The physical properties and crystalline structure of the PUs prepared from this diisocyanate were compared to their counterparts prepared from similar fatty acid-derived diisocyanate, 1,7-heptamethylene diisocyanate (HPMDI). The HDEDI based PUs demonstrated various different properties compared to those of HPMDI based PUs. For example, HDEDI based PUs exhibited a triclinic crystal form; whereas HPMDI based PUs exhibited a hexagonal crystal lattice. In addition, canola polyol-HDEDI PU demonstrated a higher tensile strength at break than that of canola polyolHPMDI, attributed to the higher degree of hydrogen bonding associated with the former sample. Nevertheless, lower Young's modulus and higher elongation in canola polyol-HDEDI PU were obtained because of the flexibility of the long chain introduced by the HDEDI diisocyanate.
ESTERAMINES AND DERIVATIVES FROM NATURAL OIL METATHESIS
-
Page/Page column 22; 32, (2012/05/20)
Esteramine compositions and their derivatives are disclosed. The esteramines comprise a reaction product of a metathesis-derived C10-C17 monounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives with a tertiary alkanolamine. Derivatives made by quaternizing, sulfonating, alkoxylating, sulfating, and/or sulfitating the esteramines are also disclosed. In one aspect, the ester derivative of the C10-C17 monounsaturated acid or octadecene-1,18-dioic acid is a lower alkyl ester. In other aspects, the ester derivative is a modified triglyceride made by self-metathesis of a natural oil or an unsaturated triglyceride made by cross-metathesis of a natural oil with an olefin. The esteramines and derivatives are valuable for a wide variety of end uses, including cleaners, fabric treatment, hair conditioning, personal care (liquid cleansing products, conditioning bars, oral care products), antimicrobial compositions, agricultural uses, and oil field applications.
Synthesis and characterization of highly functionalized symmetric aromatic hexa-ol intermediates from oleic acid
Song, Dong,Narine, Suresh S.
experimental part, p. 43 - 47 (2009/12/31)
A novel highly functionalized aromatic hexa-ol was synthesized by palladium-catalyzed cyclotrimerization of an alkyne fatty acid ester followed by LAH reduction. This polyol product is a novel monomer made from a renewable lipid raw material for the production of polyurethanes, polyesters and polyamides.