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Specification Of Bisphenol-A
| PRODUCT IDENTIFICATION | |
| CAS NO. | 80-05-7 |
| Molecular Formula | (CH3)2C(C6H4OH)2 |
| SYNONYMS |
Benzenamine4,4'-Dihydroxy-2,2-diphenylpropane; BPA; Bis(p-hydroxyphenyl)propane; Bisferol A; Isopropylidenebis(4-hydroxybenzene); 4,4'-Isopropylidene Diphenol; p,p'-Isopropylidenebisphenol; Diphenylolpropane; 1-methylethylidene)bis-Phenol;
|
| MOL WT. | 228.29 |
|
H.S. CODE |
2907.23 |
| TOXICITY | Oral rat LD50: 3250 mg/kg |
| SALES SPECIFICATION | |
| APPEARANCE | Clean, free-flowing, dust-free prills |
| PURITY | 99.85% min |
| Water | 0.1% max |
| PHENOL | 100 max (mg/kg) |
| ISOMERS | 1000 max (mg/kg) |
| BTX | 400 max (mg/kg) |
| IRON | 1 max (mg/kg) |
| MOLTEN COLOR | 20max (Pt/Co Scale) |
| ASH | 5 max (mg/kg) |
| DESCRIPTION OF BISPHENOL-A |
|
BISPHENOL-A (BPA) is produced through an acid-catalyzed condensation reaction of phenol with acetone. BISPHENOL-A (BPA) growth prospects remain bright, based on the high growth expected for CD's during the next few years and the emergence of new markets, such as polycarbonates for auto-glazing, that could develop after the turn of the century. Epoxies are projected to grow at a more modest 3 to 4 percent annual rate, based on continued wide acceptance in adhesives, powder coatings, and electrical and electronic applications. Bis-A used in flame retardants is forecast to grow 4 to 5 percent annually through the early years of the new century. In the environmental area, recent industry-sponsored research has found no evidence of biological effects from low-dose exposures to BPA.
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