| Weight | 203.024 g/mol |
|---|---|
| Formula | C8H4Cl2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Terephthaloyl chloride (100-20-9)
terephthaloyl dichloride · 1,4-phthaloyl dichloride · p-phthaloyl dichloride
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- Sigma-Aldrich - Terephthaloyl chloride25.60 - 115.50 USD
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- Molecular Layer Deposition of Poly(p-phenylene terephthalamide) Films Using Terephthaloyl Chloride and p-Phenylenediamine (Langmuir, 2008)
- Inner-shell spectroscopy of benzaldehyde, terephthalaldehyde, ethylbenzoate, terephthaloyl chloride and phosgene: models for core excitation of poly(ethylene terephthalate) (The Journal of Physical Chemistry, 1992)
- Novel soluble fluorinated aromatic polyamides derived from 2-(4-trifluoromethylphenoxy)terephthaloyl chloride with various aromatic diamines (European Polymer Journal, 2009)
- Synthesis of ternary copolyamides from aromatic diamine (mphenylenediamine, diaminodiphenylsulfone), aromatic diamine with carboxyl or sulfonic group (3,5diaminobenzoic acid, 2,4diaminobenzenesulfonic acid), and iso or terephthaloyl chloride (Journal of Applied Polymer Science, 2000)
- Self-Reguiating Poiycondensations. II. A Study of the Order Present in Polyamide-Hydrazides Derived from Terephthaloyl Chloride and p-Aminobenzhydrazide (Journal of Macromolecular Science, Part A, 1973)
- Determination of free amino group content of serum albumin microcapsules: II. Effect of variations in reaction time and in terephthaloyl chloride concentration (International Journal of Pharmaceutics, 1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - terephthaloyl dichloride
- 1,4-phthaloyl dichloride
- p-phthaloyl dichloride
-
SMILESC1=CC(=CC=C1C(=O)Cl)C(=O)Cl
-
InChIKeyLXEJRKJRKIFVNY-UHFFFAOYSA-N
- Pubchem - Terephthaloyl chloride
- Wikipedia - terephthaloyl chloride
Terephthaloyl chloride (TCL, 1,4-benzenedicarbonyl chloride) is the acid chloride of terephthalic acid and is one of two monomers used to make Kevlar(R), the other being p-Phenylenediamine. TCL is used as a key component in performance polymers and aramid fibers, where it imparts flame resistance, chemical resistance, temperature stability, light weight, and very high strength. TCL is also an effective water scavenger, used to stabilize isocyanates and urethane prepolymers.
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4-ETHYLBENZALDEHYDE
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Terephthaloyl chloride
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