Additional Properties
Hydrolytic Sensitivity 3: reacts with aqueous base Application Transesterification catalyst employed in manufacture of phthalate esters.1 Forms transparent conductive films on hot glass.2 Forms open frame macrocyclic structures with guanidine templates.3 Reference 1. Jenkins, L. et al. U.S. Patent 3,153,010, 1964. 2. Chem. Abstr. 111, 16204r; Jpn. Patent 63 257,121. 3. Natarajan, S. et al. Chem. Mater. 1999, 11, 1633. Safety
Hazard Info oral rat, LD50: 3,400 mg/kg
Packaging Under Nitrogen
Gelest, Inc.
Done
Datasheet
Description
Additional Properties
Hydrolytic Sensitivity 3: reacts with aqueous base Application Transesterification catalyst employed in manufacture of phthalate esters.1 Forms transparent conductive films on hot glass.2 Forms open frame macrocyclic structures with guanidine templates.3 Reference 1. Jenkins, L. et al. U.S. Patent 3,153,010, 1964. 2. Chem. Abstr. 111, 16204r; Jpn. Patent 63 257,121. 3. Natarajan, S. et al. Chem. Mater. 1999, 11, 1633. Safety
Hazard Info oral rat, LD50: 3,400 mg/kg
Packaging Under Nitrogen
Additional Properties
Hydrolytic Sensitivity 3: reacts with aqueous base Application Transesterification catalyst employed in manufacture of phthalate esters.1 Forms transparent conductive films on hot glass.2 Forms open frame macrocyclic structures with guanidine templates.3 Reference 1. Jenkins, L. et al. U.S. Patent 3,153,010, 1964. 2. Chem. Abstr. 111, 16204r; Jpn. Patent 63 257,121. 3. Natarajan, S. et al. Chem. Mater. 1999, 11, 1633. Safety
Hazard Info oral rat, LD50: 3,400 mg/kg
Packaging Under Nitrogen
Additional Properties
Hydrolytic Sensitivity 3: reacts with aqueous base
Application
Transesterification catalyst employed in manufacture of phthalate esters.1 Forms transparent conductive films on hot glass.2 Forms open frame macrocyclic structures with guanidine templates.3
Reference
1. Jenkins, L. et al. U.S. Patent 3,153,010, 1964. 2. Chem. Abstr. 111, 16204r; Jpn. Patent 63 257,121. 3. Natarajan, S. et al. Chem. Mater. 1999, 11, 1633.
Safety
