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HomeProduct name list1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

  • CAS NO.:2754-41-8
  • Empirical Formula: C10H8O6
  • Molecular Weight: 224.17
  • MDL number: MFCD13704912
  • EINECS: 691-475-9
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-10-28 16:48:35
1,2,4,5-Cyclohexanetetracarboxylic Dianhydride Structural

What is 1,2,4,5-Cyclohexanetetracarboxylic Dianhydride?

Chemical properties

White to Almost white powder to crystal.

The Uses of 1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

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.

What are the applications of Application

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.

General Description

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.

Synthesis

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%.

Advantages

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.

Properties of 1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

Melting point: 240°C(lit.)
Boiling point: 517.5±50.0 °C(Predicted)
Density  1.567
storage temp.  under inert gas (nitrogen or Argon) at 2-8°C
solubility  soluble in Acetone
form  powder to crystal
color  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

Safety information for 1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

Signal word Warning
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
Precautionary Statement Codes P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P280:Wear protective gloves/protective clothing/eye protection/face protection.

Computed Descriptors for 1,2,4,5-Cyclohexanetetracarboxylic Dianhydride

InChIKey LJMPOXUWPWEILS-UHFFFAOYSA-N
SMILES O1C(=O)C2CC3C(CC2C1=O)C(=O)OC3=O

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