Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство поставщик
ГПМДА структурированное изображение

ГПМДА

  • английское имя1,2,4,5-Cyclohexanetetracarboxylic Dianhydride
  • CAS №2754-41-8
  • CBNumberCB72484845
  • ФормулаC10H8O6
  • мольный вес224.17
  • EINECS691-475-9
  • номер MDLMFCD13704912
  • файл Mol2754-41-8.mol
химическое свойство
Температура плавления 240°C(lit.)
Температура кипения 517.5±50.0 °C(Predicted)
плотность 1.567
температура хранения under inert gas (nitrogen or Argon) at 2-8°C
растворимость soluble in Acetone
форма powder to crystal
цвет White to Almost white
InChI InChI=1S/C10H8O6/c11-7-3-1-4-6(10(14)16-8(4)12)2-5(3)9(13)15-7/h3-6H,1-2H2
ИнЧИКей LJMPOXUWPWEILS-UHFFFAOYSA-N
SMILES O1C(=O)C2CC3C(CC2C1=O)C(=O)OC3=O
Заявления об опасности и безопасности
кода HS 29321900
NFPA 704:
0
2 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H315:При попадании на кожу вызывает раздражение.

    H319:При попадании в глаза вызывает выраженное раздражение.

  • оператор предупредительных мер

    P264:После работы тщательно вымыть кожу.

    P280:Использовать перчатки/ средства защиты глаз/ лица.

ГПМДА химические свойства, назначение, производство

Химические свойства

White to Almost white powder to crystal.

Использование

1,2,4,5-Cyclohexanetetracarboxylic dianhydride can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development and chemical and pharmaceutical production processes.

прикладной

HPMDA can be used to synthesize polyesters that have four branches (dianhydride is hydrolysed to four carboxylic acids) for multiple functionalities, such as biodegradability, bioimaging and photoactivity.

Общее описание

1,2,4,5-Cyclohexanetetracarboxylic dianhydride (HPMDA) has a cyclohexane centre with two carboxylic anhydrides substituents sitting opposite to each other. HPMDA reacts with amines for polyimides or alternatively with alcohols for polyesters. The non-aromatic cyclohexane centre provides local excited state to the synthesized photochromic polyimides showing large contrast of the photo-switching effect (compared to fully aromatized polyimides). The polyimides derived from 1,2,4,5-cyclohexanetetracarboxylic dianhydride exhibit high proton conductivity (0.2 ± 0.01 S/cm at 298 K and 95% related humidity). Like other polyimides, the polyimides have excellent chemical and thermal resistance and are used in optical fibre claddings and substrates for microelectronics.

Синтез

Synthesis_2754-41-8
In a 100 mL three-necked flask equipped with a thermometer, a magnetic stirrer, a water separator, and a condenser tube was added 9.64 g of hydrogenatedEthylbenzene tetracarboxylate, 1mL of concentrated sulfuric acid, 5mL of acetic acid and 50mL of xylene were heated to 130??C. During the reaction, the reaction temperature was maintained at reflux, and the reaction continuously removed water for 5 hours. , cooling down to room temperature, suction filtration, filter cake washed with acetone, dried at room temperature under reduced pressure to give white solid 1,2,4,5-cyclohexane tetracarboxylic acid anhydride 4.80g, yield: 82.8%.

преимущество

Alicyclic acid anhydrides have been used as raw materials for functional polyimides and functional epoxy resins. Among them, 1,2,4,5-cyclohexanetetracarboxylic dianhydride is used as a raw material for polyimide resins exhibiting particularly good heat resistance, solvent solubility, thermoplasticity, low water absorption, dimensional stability, and like.

ГПМДА поставщик

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