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About This Item
Linear Formula:
C6H4-1,4-(COCl)2
CAS Number:
Molecular Weight:
203.02
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39050525
UNSPSC Code:
12352100
EC Number:
202-829-5
MDL number:
Beilstein/REAXYS Number:
607796
Assay:
≥99%
Form:
flakes
vapor density
7 (vs air)
Quality Segment
vapor pressure
0.02 mmHg ( 25 °C)
assay
≥99%
form
flakes
bp
266 °C (lit.)
mp
79-81 °C (lit.)
solubility
ethanol: soluble 100 mg/mL, clear, colorless
functional group
acyl chloride
SMILES string
ClC(=O)c1ccc(cc1)C(Cl)=O
InChI
1S/C8H4Cl2O2/c9-7(11)5-1-2-6(4-3-5)8(10)12/h1-4H
InChI key
LXEJRKJRKIFVNY-UHFFFAOYSA-N
General description
Terephthaloyl chloride is a highly reactive acid chloride derived from terephthalic acid. It is used as a cross-linking agent in polymer synthesis. Terephthaloyl chloride undergoes condensation reaction with difunctional α,ω-diaminopolystyrene to yield chain-extended polystyrene containing amide bonds along the polymer backbone. It undergoes interfacial reaction with bovine serum albumin to form thin cross-linked films.
Application
Terephthaloyl chloride was used in the synthesis of liquid crystalline thermosets by thermal cyclotrimerization of dicyanate compounds of ring substituted bis(4-hydroxyphenyl) terepthalates.
Legal Information
DuPont product
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
356.0 °F - closed cup
flash_point_c
180 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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