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Merck
CN

479624

4-(Phenylazo)benzoic acid

98%

Synonym(s):

4-(2-Phenyldiazenyl)benzoic acid, 4-Carboxyazobenzene, Azobenzene-4-carboxylic acid, Azoic acid, p-Phenylazobenzoic acid

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About This Item

Linear Formula:
C6H5N=NC6H4CO2H
CAS Number:
1562-93-2
Molecular Weight:
226.23
NACRES:
NA.22
PubChem Substance ID:
24871636
UNSPSC Code:
12352100
EC Number:
216-347-8
MDL number:
MFCD00020348
Assay:
98%

Key Documents

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Product Name

4-(Phenylazo)benzoic acid, 98%

InChI key

CSPTZWQFHBVOLO-CCEZHUSRSA-N

InChI

1S/C13H10N2O2/c16-13(17)10-6-8-12(9-7-10)15-14-11-4-2-1-3-5-11/h1-9H,(H,16,17)/b15-14+

SMILES string

OC(=O)c1ccc(cc1)\N=N\c2ccccc2

assay

98%

mp

247-250 °C (lit.)

functional group

carboxylic acid

Quality Level

100

Related Categories

Application

4-(Phenylazo)benzoic acid may be used in the preparation of a novel photochromic ZrO2 precursor solution.

General description

4-(Phenylazo)benzoic acid (PABA), an azobenzene derivative, is a photo-isomerisable molecule. It can be synthesized by reacting p-aminobenzoic acid with nitrosobenzene. The interaction of PABA with TiO2 and ZnO electrodes has been investigated. A photoreversible switch has been developed using dimethylamino calix[4]arene and PABA. The post functionalization of poly(hydroxyethyl acrylate) core cross-linked star polymers with PABA induces an ability to complex with α-cyclodextrin.

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCN7473
MKCG8798
MKBT0151V
MKBL1435
06228AJ

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A photoresponsive wettability switch based on a dimethylamino Calix[4]arene.
Zhang X, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 20(30), 9367-9371 (2014)
Synthesis of a new photochromic ZrO2 precursor for preparation of functional thin films.
Nishizawa K, et al.
Key Engineering Materials, 320, 175- 178 (2006)
Azobenzene-Functionalised Core Cross-Linked Star Polymers and their Host-Guest Interactions.
Tan S, et al.
Australian Journal of Chemistry, 67(1), 173-178 (2014)
Chao Luo et al.
Advanced materials (Deerfield Beach, Fla.), 30(23), e1706498-e1706498 (2018-04-25)
Organic compounds are desirable alternatives for sustainable lithium-ion battery electrodes. However, the electrochemical properties of state-of-the-art organic electrodes are still worse than commercial inorganic counterparts. Here, a new chemistry is reported based on the electrochemical conversion of nitro compounds to
New dyes for solar cells based on nanostructured semiconducting metal oxides: Synthesis and characterisation of ruthenium (II) complexes with thiol-substituted ligands.
Ohlsson J, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 148(1), 41-48 (2002)
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