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Merck
CN

274755

4-Nitrophthalic acid

92%

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About This Item

Linear Formula:
O2NC6H3(CO2H)2
CAS Number:
610-27-5
Molecular Weight:
211.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856603
EC Number:
210-215-3
Beilstein/REAXYS Number:
1882262
MDL number:
MFCD00007252

Key Documents

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Product Name

4-Nitrophthalic acid, 92%

InChI key

SLBQXWXKPNIVSQ-UHFFFAOYSA-N

InChI

1S/C8H5NO6/c10-7(11)5-2-1-4(9(14)15)3-6(5)8(12)13/h1-3H,(H,10,11)(H,12,13)

SMILES string

OC(=O)c1ccc(cc1C(O)=O)[N+]([O-])=O

assay

92%

impurities

5-8% 3-nitrophthalic acid

mp

159-161 °C (lit.)

functional group

carboxylic acid
nitro

Quality Level

200

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Application

4-Nitrophthalic acid was used in the preparation of a 2D homochiral inorganic-organic framework {[Mn(4-nitrophthalate)(4,4′-bipyridine)(H2O)]·(H2O2}n by reacting with manganese ions, and ancillary 4,4′-bipyridine ligands.

General description

The tissue-specific activity of 4-nitrophthalic acid was studied.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000401183
0000362586
0000306737
0000401183
0000362586

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Wei Li et al.
Dalton transactions (Cambridge, England : 2003), 40(27), 7147-7152 (2011-03-05)
A 2D homochiral inorganic-organic framework {[Mn(NPTA)(4,4'-bpy)(H(2)O)]·(H(2)O)(2)}(n) was prepared by assembling achiral polar 4-nitrophthalic acid, manganese ions, and ancillary 4,4'-bipyridine ligands (NPTA = 4-nitrophthalate) (4,4'-bpy = 4,4'-bipyridine). The isomorphous Zn(ii) compound was also prepared as a diamagnetic analogue. Adjacent manganese spin
Xiaoyong Wu et al.
Water environment research : a research publication of the Water Environment Federation, 85(5), 404-410 (2013-06-26)
In order to find the relationship between tissue-specific expressions of glutathione S-transferases (GSTs) and their function in preventing effects of environmental toxicants, GSTs were primarily purified by GST-Sepharose 4B affinity chromatography from liver intestine, gill, mantle, and adductor muscle of

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