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Merck
CN

186279

5-Aminoisophthalic acid

94%

Synonym(s):

5-Aminobenzene-1,3-dicarboxylic acid

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About This Item

Linear Formula:
H2NC6H3-1,3-(CO2H)2
CAS Number:
99-31-0
Molecular Weight:
181.15
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
24851211
EC Number:
202-748-5
Beilstein/REAXYS Number:
2805628
MDL number:
MFCD00002522

Key Documents

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InChI key

KBZFDRWPMZESDI-UHFFFAOYSA-N

InChI

1S/C8H7NO4/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3H,9H2,(H,10,11)(H,12,13)

SMILES string

Nc1cc(cc(c1)C(O)=O)C(O)=O

assay

94%

reaction suitability

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

application(s)

peptide synthesis

Quality Level

100

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Related Categories

Application

5-Aminoisophthalic acid (AIPA) can be used as a starting material to prepare:
  • Poly(5-aminoisophthalic acid) by oxidative polymerization reaction.
  • Poly(benzimidazole-co-aniline) (PBIANI) by condensation polymerization with 3,3′-diaminobenzidine via poly(5-aminoisophthalic acid) as a key intermediate.

It can also be used as a blended material with polyvinylalcohol to prepare silica-functionalized composite membranes for diffusion dialysis applications. AIPA based metal-organic framework (MOF) can be modified with various functional groups for different applications.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000213762
0000213762
0000363994
0000363993
0000357225

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A copper based metal-organic framework: Synthesis, modification and VOCs adsorption
Xu Wei-Qin, et al.
Inorganic Chemistry Communications, 92(1-2), 1-4 (2018)
Novel silica-functionalized aminoisophthalic acid-based membranes for base recovery via diffusion dialysis
Mondal AN, et al.
Journal of Membrane Science , 507(1-2), 90-98 (2016)
En Tang et al.
Inorganic chemistry, 45(16), 6276-6281 (2006-08-02)
Two stable supramolecular microporous cobalt(II) polymers, namely [Co(HAIP)2]n.3nH2O (1) and [Co(AIP)(H2O)]n (2), AIP = 5-aminoisophthalate, were hydrothermally synthesized and characterized by single-crystal X-ray diffraction, IR spectra, thermogravimetric analyses, and variable-temperature magnetic susceptibility measurements. The two complexes are constructed from the
Zohreh Moradi et al.
The Analyst, 144(14), 4351-4361 (2019-06-14)
In the present work, a simple and rapid method, namely magnetic dispersive micro-solid phase extraction (MD-μ-SPE), was developed using magnetic Fe3O4@SiO2@Ti-MOF (metal-organic framework)-nanocomposites (NCs) as a viable and efficient sorbent to pre-concentrate and assess caffeic acid (CA) in the medical
A J Dobson et al.
Acta crystallographica. Section C, Crystal structure communications, 54 ( Pt 10), 1503-1505 (1998-11-10)
The title acid, C8H7NO4.0.5H2O, crystallized in the centrosymmetric space group C2/c in a zwitterionic form (5-ammonioisophthalate), with the water molecule on a twofold axis. The three ammonio H atoms and the H atom on the remaining carboxyl group, which are
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