From Surf Wiki (app.surf) — the open knowledge base
Isophthalic acid
meta-Phthalic acid Phthalic acid (ortho) Terephthalic acid (para) Trimesic acid
Isophthalic acid is an organic compound with the formula C6H4(CO2H)2. This colorless solid is an isomer of phthalic acid and terephthalic acid. The main industrial uses of purified isophthalic acid (PIA) are for the production of polyethylene terephthalate (PET) resin and for the production of unsaturated polyester resin (UPR) and other types of coating resins.
Isophthalic acid is one of three isomers of benzenedicarboxylic acid, the others being phthalic acid and terephthalic acid.
Crystalline isophthalic acid is built up from molecules connected by hydrogen bonds, forming infinite chains.
Preparation
Isophthalic acid is produced on the billion kilogram per year scale by oxidizing meta-xylene using oxygen.
In the laboratory, chromic acid can be used as the oxidant. It also arises by fusing potassium meta-sulfobenzoate, or meta-bromobenzoate with potassium formate (terephthalic acid is also formed in the last case).
The barium salt, as its hexahydrate, is very soluble in water (a distinction between phthalic and terephthalic acids). Uvitic acid, 5-methylisophthalic acid, is obtained by oxidizing mesitylene or by condensing pyroracemic acid with baryta water.
Applications
Aromatic dicarboxylic acids are used as precursors (in the form of acyl chlorides) to commercially important polymers, e.g. the fire-resistant material Nomex. Mixed with terephthalic acid, isophthalic acid is used in the production of PET resins for drink plastic bottles and food packaging. The high-performance polymer polybenzimidazole is produced from isophthalic acid. Also, the acid is used as an important input to produce insulation materials.
References
Note: reference 2 refers to the ortho isomer. Accurate cites for the meta isomer not available.
References
- Brown, H.C., et al., in Baude, E.A. and Nachod, F.C., ''Determination of Organic Structures by Physical Methods'', Academic Press, New York, 1955.
- GHS: [https://gestis.dguv.de/data?name=037130 GESTIS 037130]
- (1974). "The crystal structure of isophthalic acid". Acta Crystallogr..
- "Lotte Chemical to invest $3.2mn to beef up meta-xylene and polycarbonate production".
- (2007). "Phthalic Acid and Derivatives".
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Isophthalic acid — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report