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Terephthalic Acid

Cat.No ACM100210-1

Basic Information Description Application Features And Benefits
CAS 100-21-0
Catalog Number ACM100210-1
Synonyms TEREPHTHALIC ACID FOR SYNTHESIS;Terephthalic acid;Terephthalicacid;TEREPHTHALIC ACID/BENZENE-1,4-DICARBOXYLIC ACID;p-Phthalic acid
IUPAC Name terephthalic acid
Molecular Weight 166.13
Molecular Formula C8H6O4
Canonical SMILES OC(=O)c1ccc(cc1)C(O)=O
InChI 1S/C8H6O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H,(H,9,10)(H,11,12)
InChI Key KKEYFWRCBNTPAC-UHFFFAOYSA-N
Boiling Point greater than 572 °F at 760 mm Hg (sublimes without melting) (NTP, 1992);>572°F (sublimes)
Melting Point 300ºC
Flash Point 260ºC
Purity 99%
Density 1.51
Solubility Insoluble (NTP, 1992);9.03e-05 M;Insoluble in chloroform, ether, acetic acid; slightly soluble in alcohol; soluble in alkalies;Solubilities at 25 °C (g/100 g solvent): water = 0.0017, glacial acetic acid = 0.013, methanol = 0.1, dimethylformamide = 6.7, dimethyl sulfoxide = 19.0;In water, 15 mg/L at 20 °C;0.015 mg/mL at 20 °C;Solubility in water, g/100ml at 20 °C: 0.28
Appearance White to Almost white powder to crystal
Storage Store under inert gas, 2-8°C
Assay 98%
Autoignition Temperature 925 °F
Beilstein REAXYS Number 1909333
EC Number 202-830-0
Form powder
MDL Number MFCD00002558
NACRES NA.23
Packaging Packaging
5, 100, 500 g in poly bottle
PubChem ID 24850686
Quality Level 100
Refractive Index 1.648
Vapor Pressure <0.01 mm Hg ( 20 °C)
Description Terephthalic acid (a portmanteau of the turpentine producing tree terebinthus, and phthalic acid) is the organic compound with formula C6H4(CO2H)2. This White solid is a commodity chemical, used principally as a precursor to the polyester PET, used to make clothing and plastic bottles. Several million tonnes are produced annually.
Application Terephthalic acid (TPA) can be synthesized from bio-based materials for a variety of s, which include the production of polyester fiber, non-fiber field, PET bottles, synthetic perfumes and medicines.
Terephthalic acid is used as a linker molecule in the preparation of metal organic frameworks (MOFs).
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