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Terephthalic acid



Terephthalic acid
Other names Benzene-1,4-dicarboxylic acid
para-Phthalic acid
TPA
PTA
Identifiers
CAS number 100-21-0
RTECS number WZ0875000
SMILES C1=CC(=CC=C1C
(=O)O)C(=O)O
Properties
Molecular formula C6H4(COOH)2
Molar mass 166.13 g/mol
Appearance white crystals or powder
Density 1.522 g/cm³
Melting point

427°C in a sealed tube (sublimes at 402°C (675 K) in air)

Boiling point

sublimes

Solubility in water 1.7g in 100g H2O at 25°C
Solubility Soluble in Dimethyl sulfoxide, DMF, and alkalies. Slightly soluble in ethanol, methanol, formic acid and sulfuric acid. [1]
Acidity (pKa) 3.54 at 25°C [2]
Structure
Dipole moment zero
Hazards
MSDS External MSDS
EU classification not listed
Related Compounds
Related carboxylic acids Phthalic acid
Isophthalic acid
Benzoic acid
p-Toluic acid
Related compounds p-Xylene
Polyethylene terephthalate
Dimethyl terephthalate
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Terephthalic acid is one isomer of the three phthalic acids. It finds important use as a commodity chemical, principally as a starting compound for the manufacture of polyester (specifically PET), used in clothing and to make plastic bottles. It is also known as 1,4-benzenedicarboxylic acid, and it has the chemical formula C6H4(COOH)2. It has recently become an important component in the development of hybrid framework materials.

Additional recommended knowledge

Contents

History

Phthalic acid (the ortho isomer of terephthalic acid) was obtained by French chemist Auguste Laurent in 1836 by oxidizing naphthalene tetrachloride, and, believing the resulting substance to be a naphthalene derivative, he named it naphthalenic acid. Swiss chemist Jean Charles Galissard de Marignac determined its formula and showed Laurent’s supposition to be incorrect, upon which Laurent gave it its present name.

Properties

It is almost insoluble in water, alcohol and ether; it sublimes rather than melting when heated. This insolubility makes it relatively awkward to work with, and up until around 1970 much crude terephthalic acid was converted to the dimethyl ester for purification.

Production

Terephthalic acid can be formed in the laboratory by oxidizing para-diderivatives of benzene, or best by oxidizing caraway oil, a mixture of cymene and cuminol, with chromic acid.


On an industrial scale, terephthalic acid is produced, similar to benzoic acid, by oxidation of p-xylene by oxygen from air. This is done using acetic acid as solvent, in the presence of a catalyst such as cobalt-manganese, using a bromide promoter. Alternatively, it can be made via the Henkel process, which involves the rearrangement of phthalic acid to terephthalic acid via the corresponding potassium salts. The terephthalic acid is and dimethyl terephthalate, in turn, often used as a monomer component in the production of polymers, principally polyethylene terephthalate (polyester or PET). World production in 1970 was around 1.75 million tonnes.[2]. By 2006, global PTA demand had substantially exceeded 30 million tonnes.

References

  1. ^ Sheehan, R.J. Terephthalic acid, dimethyl phthalate and isophthalic acid. In: Ullmann's encyclopedia of industrial chemistry. 5th completely revised ed. Vol. A 26. VCH Verlagsgesellschaft, 1995. p. 193-204
  2. ^ http://www.intox.org/databank/documents/chemical/terephac/cie474.htm
  1. 1911 Encyclopedia
  2. Basic Organic Chemistry: Part 5, Industrial Products, J.M. Tedder, A. Nechvatal, A.H. Tubb (editors), John Wiley & Sons, Chichester, UK (1975).
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Terephthalic_acid". A list of authors is available in Wikipedia.
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