Detail of > 89-32-7
- CAS Number:
- 89-32-7
- Name:
1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone
- Superlist Name:
- 1,2,4,5-Benzenetetracarboxylic anhydride
- Formula:
- C10H2O6
- Molecular Structure:
![Molecular Structure of 89-32-7 (1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone)](http://www.lookchem.com/300w/2010/0713/89-32-7.jpg)
- Synonyms:
- 1,2,4,5-Benzenetetracarboxylic1,2:4,5-dianhydride (8CI);Pyromellitic 1,2:4,5-dianhydride (6CI);1,2,4,5-Benzenetetracarboxylic acid 1,2:4,5-dianhydride;1,2,4,5-Benzenetetracarboxylic acid dianhydride;1,2:4,5-Benzenetetracarboxylicdianhydride;NSC 4798;PMDA;PMDA-M;Pyromellitic acid anhydride;Pyromelliticacid dianhydride;Pyromellitic anhydride;Pyromellitic dianhydride;
- Molecular Weight:
- 218.12
- EINECS:
- 201-898-9
- Density:
- 1.885 g/cm3
- Melting Point:
- 283-286 °C(lit.)
- Boiling Point:
- 398.6 °C at 760 mmHg
- Flash Point:
- 183.5 °C
- Solubility:
- decomposes in water
- Appearance:
- White powder
- Hazard Symbols:
Xn- Risk Codes:
- 41-42/43
- Safety:
- 22-24-26-37/39Details
- Deleted CAS:
- 159104-96-8
Related products
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Reference
- Aromatic polyester-polycarbonate blends for molding
- Aromatic polyester-polycarbonate blends for molding. (Toyobo Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 59157146 A2 6 Sep 1984 Showa, 6 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C08L067-02; C08K005-09; C08L069-00. ICI: C08L067-02, C08L069-00; C08L069-00, C08L067-02. APPLICATION: JP 83-31523 26 Feb 1983. DOCUMENT TYPE: Patent CA Section: 37 (Plastics Manufacture and Processing) A 30--70 blend of an ethylene terephthalate-based polyester and a polycarbonate contg. 0.005-0.05 phr carboxylic acid (or its deriv.) is easily pelletized and gives a transparent product. Thus, 6:4 blend of poly(ethylene terephthalate) [25038-59-9] (intrinsic viscosity 0.6 in 6:4 PhOH-C2H2Cl4 at 30°) and a polycarbonate (mol. wt. 24,000) was dried at 130°/2 mm for 19 h, dry blended with 0.05 phr pyromellitic anhydride (I) [89-32-7] and kneaded at 280° to give a continuous strand without breaking. A pelletized strand was injection molded to give a sample (thickness 1/8 in) exhibiting transparency 70.6% and haze 51.6% , compared with 48.2% and 82.5%, resp., with discontinuous strand, for a blend not contg. I.
- Polyimides from diisocyanates, dianhydrides, and their dialkyl esters
- Polyimides from diisocyanates, dianhydrides, and their dialkyl esters. Alvino, William M.; Edelman, Leonard E. (Polymers Plast. Dep., Westinghouse Res. 89-32-7 are also occured in this study. Lab., Pittsburgh, Pa., USA). J. Appl. Polym. Sci., 22(7), 1983-90 (English) 1978. CODEN: JAPNAB. ISSN: 0021-8995. DOCUMENT TYPE: Journal CA Section: 36 (Plastics Manufacture and Processing) High mol. wt. polyimides can be produced by the reaction of diisocyanates with a mixt. of arom. dianhydrides and their dialkyl esters. The reaction works well with pyromellitic dianhydride [89-32-7], benzophenone tetracarboxylic dianhydride [2421-28-5] and trimellitic anhydride [552-30-7] and their Me and Bu esters as well as mixts. of these. The polyimides are identical to those prepd. from dianhydrides and diamines. A catalyst is not necessary, but high mol. wt. depends on the anhydride-ester ratio and temp. Tough, flexible films can be prepd. from pptd. and redissolved polymer solns. .
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