B4007
1,2,4,5-Benzenetetracarboxylic acid
96%
Synonym(s):
Pyromellitic acid
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All Photos(3)
About This Item
Linear Formula:
C6H2(CO2H)4
CAS Number:
Molecular Weight:
254.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
96%
form
powder
mp
281-284.5 °C (lit.)
SMILES string
OC(=O)c1cc(C(O)=O)c(cc1C(O)=O)C(O)=O
InChI
1S/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)
InChI key
CYIDZMCFTVVTJO-UHFFFAOYSA-N
Application
1,2,4,5-Benzenetetracarboxylic acid is extensively used as a ligand in the synthesis of a wide range of metal-organic frameworks (MOFs) and coordination polymers. It can also be used to prepare supramolecular hydrogels by synthesizing gelators reacting 1,2,4,5-benzenetetracarboxylic acid with 4-hydroxy pyridine.
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
617.0 °F
Flash Point(C)
325 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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K-J Westin et al.
Journal of colloid and interface science, 282(2), 359-369 (2004-12-14)
The influence of four calcium complexing substances, i.e., citric acid (CIT), diethylenetriaminepentaacetic acid (DTPA), ethylenediaminetetraacetic acid (EDTA) and pyromellitic acid (PMA), on the crystal growth rate of the calcium carbonate polymorphs aragonite and calcite has been studied. Using a seeded
New hydrogen-bonded supramolecular hydrogels and fibers derived from 1, 2, 4, 5-benzenetetracarboxylic acid and 4-hydroxypyridine.
Wang Y, et al.
Chemistry Letters (Jpn), 35(5), 548-549 (2006)
S Mallet et al.
Journal of chromatography. A, 853(1-2), 181-184 (1999-09-16)
Tartaric acid, used in pharmaceuticals and industrial food preparation, is an important by-product of wine preparation. It is produced by wine factories in large quantities and cannot be rejected into the environment. Wineries precipitate tartaric acid using calcium hydroxide and
New Two-Dimensional Metal? Organic Networks Constructed from 1, 2, 4, 5-Benzenetetracarboxylate and Chelate Ligands.
Li Y, et al.
Inorganic Chemistry, 42(9), 3119-3124 (2003)
Jacek Gawroński et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(11), 2484-2494 (2002-08-16)
The chiral but highly symmetrical acyclic and cyclic pyromellitic diimide dimers and trimers 2-5 have been obtained and characterized for the first time. The pyromellitdiimide chromophores in these molecules are linked by a rigid diequatorially 1,2-disubstituted cyclohexane skeleton. The structures
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