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89-05-4

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89-05-4 Usage

Chemical Properties

White powder. Absorbs moisture slowly if exposed to atmosphere. Soluble in alcohol, slightly soluble in water.

Uses

Different sources of media describe the Uses of 89-05-4 differently. You can refer to the following data:
1. Pyromellitic acid (PMA) is mainly used as intermediate for powder coating. Product Data Sheet
2. 1,2,4,5-benzenetetracarboxylic acid is used for the synthesis of the polyimide, pyromellitic octyl, etc., it is the main raw material of matting curing agent.
3. Pyromellitic acid is an eluent used in anion chromatography and forms complexes with magnesium and calcium ions. It is used as a curing agent, as an intermediate for powder coating and a cross-linking agent for alkyd resin. It is involved in the synthesis of polyimide and pyromellitic octyl.

Definition

ChEBI: A tetracarboxylic acid that is benzene substituted by four carboxy groups at positions 1, 2, 4 and 5 respectively.

Hazard

Skin irritant, may be carcinogenic.

Purification Methods

Dissolve it in 5.7 parts of hot dimethylformamide, decolorise, filter and cool. The precipitate is collected and dried in air. The solvent is removed by heating in an oven at 150-170o for several hours. It also crystallises from water. [Beilstein 9 H 997, 9 IV 3804.]

Check Digit Verification of cas no

The CAS Registry Mumber 89-05-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89-05:
(4*8)+(3*9)+(2*0)+(1*5)=64
64 % 10 = 4
So 89-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H6O8/c11-7(12)3-1-4(8(13)14)6(10(17)18)2-5(3)9(15)16/h1-2H,(H,11,12)(H,13,14)(H,15,16)(H,17,18)/p-4

89-05-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B23099)  Pyromellitic acid, 96%   

  • 89-05-4

  • 100g

  • 265.0CNY

  • Detail
  • Alfa Aesar

  • (B23099)  Pyromellitic acid, 96%   

  • 89-05-4

  • 500g

  • 956.0CNY

  • Detail

89-05-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name pyromellitic acid

1.2 Other means of identification

Product number -
Other names 1,2,4,5-Benzenetetracarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89-05-4 SDS

89-05-4Relevant articles and documents

-

Cava et al.

, p. 2524,2525 (1960)

-

Structural diversity and luminescent sensing of three coordination polymers based on the hydrolysates of N,N′-bis(3,5-dicarboxylatophenyl)pyromelliticdi-imide)

Fan, Liming,Wang, Jiang,Zhao, Li,Zhang, Yujuan,Wang, Xiaoqing,Hu, Tuoping,Zhang, Xiutang

, p. 54 - 61 (2018)

Based on the hydrolysates of N,N′-bis(3,5-dicarboxylatophenyl)pyromelliticdi-imide) (H4L) and 1,3-bis(imidazol-1-ylmethyl)benzene (bimb), three coordination polymers, namely, {[Zn(BTC)0.5(bimb)]·4H2O}n (1), [Cu(BTC)0.5(bimb)]n (2), and {[Cd(AIP)(H2O)]·H2O}n (3), have been obtained under solvothermal conditions. The possible hydrolysis mechanism of H4L was investigated here. Structural analyses reveal that complex 1 is a 3D (4,4)-c {64.82}{66}2-bbf net. Complex 2 displays a 2D 4-c {32.62.72}-kgm sheet. While complex 3 exhibits a 3D (3,6)-c {4.62}2{42.610.83}-rtl net based on binuclear {Cd2(COO)4} SBUs. Besides, luminescent sensing investigation indicated that 1 and 3 exhibit highly sensitive and selective sensing of chromate anions in aqueous solution.

Hydrothermal Generation of Conjugated Polymers Using the Example of Pyrrone Polymers and Polybenzimidazoles

Gl?cklhofer, Florian,Mezzavilla, Stefano,Taublaender, M. Josef,Thiele, Sophia,Unterlass, Miriam M.

supporting information, p. 15050 - 15060 (2020/05/18)

Various polyimides and polyamides have recently been prepared via hydrothermal synthesis in nothing but H2O under high-pressure and high-temperature conditions. However, none of the prepared polymers feature a truly conjugated polymer backbone. Here, we report on an expansion of the synthetic scope of this straightforward and inherently environmentally friendly polymerization technique to the generation of conjugated polymers. Selected representatives of two different polymer classes, pyrrone polymers and polybenzimidazoles, were generated hydrothermally. We present a mechanistic discussion of the polymer formation process as well as an electrochemical characterization of the most promising product.

Method for preparing pyromellitic acid through catalytic oxidation using Anderson heteropoly acid

-

Paragraph 0011; 0037; 0038; 0039 0040; 0041; 0041-0046, (2018/07/30)

The invention discloses a method for preparing pyromellitic acid through catalytic oxidation using Anderson heteropoly acid. The method comprises the following specific steps: 1), mixing mesitylene, acatalyst, an additive and a solvent, and then performin an oxidation reaction under the action of an oxidant, wherein the oxidation reaction temperature is 80-130 DEG C, the gauge pressure is 1.0-4.0MPa, and the reaction time is 7-24h; 2), after the oxidation reaction is completed, filtering to remove the catalyst, adding an extracting reagent and water, and extracting to obtain an organic phaseand an aqueous phase, and concentrating and purifying the organic phase to obtain the pyromellitic acid, wherein the catalyst is the Anderson-type heteropoly acid. The reaction condition is mild, hydrogen peroxide, air or oxygen is used as the oxidant, environment friendliness is achieved, the product yield is high, the catalyst reactivity is high, the specificity is good, recycling is achieved, and operation is simple, so that the method is suitable for industrial production.

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