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Merck
CN

120871

对苯二甲酰氯

≥99%, flakes

别名:

Terephthalic acid chloride, Terephthaloyl dichloride

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关于此项目

线性分子式:
C6H4-1,4-(COCl)2
化学文摘社编号:
100-20-9
分子量:
203.02
NACRES:
NA.22
PubChem Substance ID:
24847435
eCl@ss:
39050525
UNSPSC Code:
12352100
EC Number:
202-829-5
MDL number:
MFCD00000693
Beilstein/REAXYS Number:
607796

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产品名称

对苯二甲酰氯, ≥99%, flakes

InChI key

LXEJRKJRKIFVNY-UHFFFAOYSA-N

InChI

1S/C8H4Cl2O2/c9-7(11)5-1-2-6(4-3-5)8(10)12/h1-4H

SMILES string

ClC(=O)c1ccc(cc1)C(Cl)=O

vapor density

7 (vs air)

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

Quality Level

200

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相关类别

Application

对苯二甲酰氯通过环状取代 双 （4-羟基苯基）对苯二甲酸酯的二氰酸酯化合物进行热环三聚反应，以用于合成液晶热固性化合物 。

General description

对苯二甲酰氯是一种源自对苯二甲酸的高反应性酰氯。它在聚合物合成中用作交联剂。对苯二甲酰氯与双官能团α,ω-二氨基聚苯乙烯发生缩合反应，沿着聚合物主链生成含有酰胺键的扩链聚苯乙烯。它与牛血清白蛋白发生界面反应，形成交联薄膜。

Legal Information

DuPont 产品

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

存储类别

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB6373
SDBB5179
SDBB0186
STBL4186
SDBB0343

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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
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)
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
Greeshma Nair et al.
Chembiochem : a European journal of chemical biology, 7(11), 1683-1689 (2006-10-20)
We report a novel technique for preparing cross-linked protein membranes within microchannels by using an interfacial cross-linking reaction. Glass microchannels with a Y input were assembled by using a simple adhesive bonding technique to achieve dual, parallel laminar flows. Membrane
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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