Terephthaloyl chloride, 99%
Terephthaloyl chloride, 99%
Terephthaloyl chloride, 99%
Thermo Scientific Chemicals

Terephthaloyl chloride, 99%

CAS: 100-20-9 | C8H4Cl2O2 | 203.02 g/mol
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Catalog NumberQuantity
A11224.30
also known as A11224-30
250 g
Catalog number A11224.30
also known as A11224-30
Price (CNY)
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Quantity:
250 g
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Chemical Identifiers
CAS100-20-9
IUPAC Namebenzene-1,4-dicarbonyl dichloride
Molecular FormulaC8H4Cl2O2
InChI KeyLXEJRKJRKIFVNY-UHFFFAOYSA-N
SMILESClC(=O)C1=CC=C(C=C1)C(Cl)=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Formcrystalline flakes or powder
Assay (GC)> 98.5%
Assay (Titration ex Chloride)> 98.5%
Terephthaloyl chloride acts as a monomer with p-phenylenediamine used in the preparation of polymer viz. poly paraphenylene terephthalamide. It is an active component in performance polymers and aramid fibers, which gives flame resistance, chemical resistance, temperature stability, light weight, and very high strength. It is also used as an effective water scavenger, utilized to stabilize isocyanates and urethane prepolymers. Further, it is used in the preparation of liquid crystalline thermosets by thermal cyclotrimerization of dicyanate compounds of ring substituted bis(4-hydroxyphenyl) terepthalates. In addition to this, it is involved in the condensation reaction with difunctional alfa, μ-diaminopolystyrene to get chain-extended polystyrene containing amide bonds along the polymer backbone.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Terephthaloyl chloride acts as a monomer with p-phenylenediamine used in the preparation of polymer viz. poly paraphenylene terephthalamide. It is an active component in performance polymers and aramid fibers, which gives flame resistance, chemical resistance, temperature stability, light weight, and very high strength. It is also used as an effective water scavenger, utilized to stabilize isocyanates and urethane prepolymers. Further, it is used in the preparation of liquid crystalline thermosets by thermal cyclotrimerization of dicyanate compounds of ring substituted bis(4-hydroxyphenyl) terepthalates. In addition to this, it is involved in the condensation reaction with difunctional alfa, µ-diaminopolystyrene to get chain-extended polystyrene containing amide bonds along the polymer backbone.

Solubility
Soluble in ethanol, ether and other common organic solvents.

Notes
Incompatible with alcohols, oxidizing agents, water and strong bases.
RUO – Research Use Only

General References:

  1. Ali, W.; Kausar, A.; Iqbal, T. Reinforcement of high performance polystyrene/polyamide/polythiophene with multi-walled carbon nanotube obtained through various routes. Compos. Interfaces 2015, 22 (9), 885-897.
  2. Wan, J.; Gan, B.; Li, C.; Molina-Aldareguia, J.; Li, Z.; Wang, X.; Wang, D. Y. A novel biobased epoxy resin with high mechanical stiffness and low flammability: synthesis, characterization and properties. J. Mater. Chem. A 2015, 3 (43), 21907-21921.