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311278

Sigma-Aldrich

5-Hydroxyisophthalsäure

97%

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About This Item

Lineare Formel:
HOC6H3-1,3-(CO2H)2
CAS-Nummer:
618-83-7
Molekulargewicht:
182.13
EG-Nummer:
210-565-7
MDL-Nummer:
MFCD00002515
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24858506
NACRES:
NA.22

Qualitätsniveau

100

Assay

97%

mp (Schmelzpunkt)

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)

InChIKey

QNVNLUSHGRBCLO-UHFFFAOYSA-N

Allgemeine Beschreibung

The hydrothermal reaction of 5-hydroxyisophthalic acid, Co(II)/Cu(II) and dipyridophenazine, that forms two 3D chiral coordination polymers, was studied.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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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)
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
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
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
Kaisa R Hänninen et al.
Journal of pharmaceutical sciences, 96(1), 117-131 (2006-09-13)
The effect of valence of mobile counter-ions (extracting electrolytes), mobile co-ions, and drug-like compounds was evaluated on drug binding/release in ion-exchange fibers. The experimental results support the Donnan theory and suggest that incorporation of monovalent salicylic acid (SA) and divalent
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