I19403
间苯二甲酰氯
≥99%
别名:
间苯二酰二氯
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关于此项目
线性分子式:
C6H4-1,3-(COCl)2
化学文摘社编号:
分子量:
203.02
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-774-7
Beilstein/REAXYS Number:
638342
MDL number:
InChI
1S/C8H4Cl2O2/c9-7(11)5-2-1-3-6(4-5)8(10)12/h1-4H
InChI key
FDQSRULYDNDXQB-UHFFFAOYSA-N
SMILES string
ClC(=O)c1cccc(c1)C(Cl)=O
vapor pressure
0.03 mmHg ( 25 °C)
assay
≥99%
expl. lim.
8.9 %
bp
276 °C (lit.)
mp
43-44 °C (lit.)
Quality Level
General description
异酞菁氯在多种聚合反应中起交联剂的作用。
Application
与异酞菁氯化物反应;
- 利用聚乙烯胺生产PA-100膜
- Epiamine，一种聚醚胺，可用于生产PA-300膜
- 利用1,3-二氨基-4-氯苯生成聚酰胺
- 利用三聚氰胺生成聚酰胺气凝胶
- 双胺，产生间苯二甲酰胺类化合物
- 对苯二甲酰氯和双酚型重氮萘醌（DNQ）缩聚成含有DNQ结构的多芳基化合物
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Eye Dam. 1 - Skin Corr. 1A
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
此项目有
Utilization of Polyarylates Having Chemically Introduced Diazonaphthoquinone Structure for Reaction Development Patterning
Oyama T, et al.
J. Photopolym. Sci. Technol., 28(2), 219-227 (2015)
The rapid synthesis and dynamic behaviour of an isophthalamide [2] catenane
Marrs CN and Evans NH
Organic & Biomolecular Chemistry (2015)
Constitutional isomerism in polyamides derived from isophthaloyl chloride and 1, 3-diamine-4-chlorobenzene.
Garcia JM, et al.
Journal of Polymer Science, 41(9), 1202-1215 (2003)
Rapid and facile synthesis of a low-cost monolithic polyamide aerogel via sol-gel technology
He S, et al.
Materials Letters, 144, 82-84 (2015)
Naylor T deV
Polymer Membranes: Materials, Structures and Separation Performance null
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