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About This Item
Linear Formula:
HOC6H3-1,3-(CO2H)2
CAS Number:
Molecular Weight:
182.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
298-302 °C (lit.)
SMILES string
OC(=O)c1cc(O)cc(c1)C(O)=O
InChI
1S/C8H6O5/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)
InChI key
QNVNLUSHGRBCLO-UHFFFAOYSA-N
Related Categories
General description
The hydrothermal reaction of 5-hydroxyisophthalic acid, Co(II)/Cu(II) and dipyridophenazine, that forms two 3D chiral coordination polymers, was studied.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Mamoru Yamada et al.
Biotechnology letters, 32(3), 445-450 (2009-11-27)
5-Hydroxyisophthalic acid-producing microorganisms were isolated from enrichment cultures using 5-sulfoisophthalic acid as a sulfur source. One bacterium, Ochrobactrum anthropi S9, had the highest 5-sulfoisophthalic acid-degrading activity, and stoichiometrically formed 5-hydroxyisophthalic acid, a raw material for polymer synthesis. Under optimum culture
Mathias Köberl et al.
Dalton transactions (Cambridge, England : 2003), 40(43), 11490-11496 (2011-09-29)
The treatment of the dimeric paddle-wheel (PW) compound [Mo(2)(NCCH(3))(10)][BF(4)](4)1 with oxalic acid (0.5 equiv.), 1,1-cyclobutanedicarboxylic acid (1 equiv.), 5-hydroxyisophthalic acid (1 equiv.) (m-bdc-OH) or 2,3,5,6-tetrafluoroterephthalic acid (0.5 or 1 equiv.) leads to the formation of macromolecular dicarboxylate-linked (Mo(2))(n) entities (n
Kaisa Hänninen et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 31(5), 306-317 (2007-06-22)
Donnan theory was applied to gain mechanistic understanding on the factors affecting drug loading process, compound-fiber affinity and subsequent release from fibrous ion-exchangers. Impact of initial loading solution concentration on fiber occupancy and loading efficiency of compounds were assessed experimentally
Jiyoung Lee et al.
Nature communications, 8, 14070-14070 (2017-01-05)
Self-assembly has proven to be a widely successful synthetic strategy for functional materials, especially for metal-organic materials (MOMs), an emerging class of porous materials consisting of metal-organic frameworks (MOFs) and metal-organic polyhedra (MOPs). However, there are areas in MOM synthesis
Zheng-Bo Han et al.
Dalton transactions (Cambridge, England : 2003), (44)(44), 9807-9811 (2009-11-04)
The hydrothermal reaction of Co(II)/Cu(II), 5-hydroxyisophthalic acid and dipyridophenazine leads to the generation of two 3D chiral coordination polymers, [M(hip)(DPPZ)](n) (M = Co(), Cu(), H(2)hip = 5-hydroxyisophthalic acid, DPPZ = dipyridophenazine), which contain M-hip-M helical chains (M = Co, Cu)
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