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Documenti fondamentali

120871

Sigma-Aldrich

Terephthaloyl chloride

≥99%, flakes

Sinonimo/i:

Terephthalic acid chloride, Terephthaloyl dichloride

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About This Item

Formula condensata:
C6H4-1,4-(COCl)2
Numero CAS:
Peso molecolare:
203.02
Beilstein:
607796
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
eCl@ss:
39050525
ID PubChem:
NACRES:
NA.22

Densità del vapore

7 (vs air)

Tensione di vapore

0.02 mmHg ( 25 °C)

Saggio

≥99%

Stato

flakes

P. ebollizione

266 °C (lit.)

Punto di fusione

79-81 °C (lit.)

Solubilità

ethanol: soluble 100 mg/mL, clear, colorless

Gruppo funzionale

acyl chloride

Stringa SMILE

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
LXEJRKJRKIFVNY-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

Terephthaloyl chloride was used in the synthesis of liquid crystalline thermosets by thermal cyclotrimerization of dicyanate compounds of ring substituted bis(4-hydroxyphenyl) terepthalates.

Note legali

DuPont product

Pittogrammi

Skull and crossbonesCorrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Inhalation - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

356.0 °F - closed cup

Punto d’infiammabilità (°C)

180 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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N V Larionova et al.
International journal of pharmaceutics, 189(2), 171-178 (1999-10-28)
The objective of this study is to demonstrate the feasibility of microcapsules containing a protein and a proteinase inhibitor in order to allow the oral administration of proteic or peptidic drug. Starch/bovine serum albumin mixed-walled microcapsules were prepared using interfacial
D Hettler et al.
Journal of microencapsulation, 11(2), 213-224 (1994-03-01)
Microcapsules were prepared from three proteins, namely human serum albumin (HSA), bovine fibrinogen and ovalbumin, by an interfacial crosslinking process using terephthaloylchloride. They were further treated with alkaline hydroxylamine in order to disrupt ester and anhydride bonds in the walls.
N Pariot et al.
International journal of pharmaceutics, 211(1-2), 19-27 (2001-01-04)
Microcapsules were prepared by interfacial cross-linking of beta-cyclodextrins (beta-CD) with terephthaloyl chloride (TC). Batches were prepared from beta-CD solutions in 1 M NaOH, using 5% TC and a 30 min reaction time. Microcapsules were studied with respect to morphology (microscopy)
M C Levy et al.
Journal of pharmaceutical sciences, 80(6), 578-585 (1991-06-01)
Fourier transform infrared (FT-IR) spectroscopic studies were performed on microcapsules prepared through interfacial cross-linking of human serum albumin (HSA) with terephthaloylchloride at various pH values (5.9 to 11). Correlations were established with morphology and size of microcapsules. Increasing polycondensation pH
Synthesis of well-defined azido and amino end-functionalized polystyrene by atom transfer radical polymerization.
Matyjaszewski K, et al.
Macromolecular Rapid Communications, 18(12), 1057-1066 (1997)

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Molecular Layer Deposition of Organic and Hybrid Organic-Inorganic Polymers

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