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H5126

Sigma-Aldrich

2-(4-Hydroxyphenylazo)benzoic acid

≥90% (HPLC)

Synonym(s):

2-(4′-Hydroxybenzeneazo)benzoic acid, 4′-Hydroxyazobenzene-2-carboxylic acid, HABA, HBABA

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About This Item

Linear Formula:
HOC6H4N=NC6H4CO2H
CAS Number:
1634-82-8
Molecular Weight:
242.23
Beilstein:
1842696
EC Number:
216-655-2
MDL number:
MFCD00002428
UNSPSC Code:
12352100
PubChem Substance ID:
57654257
NACRES:
NA.22

Assay

≥90% (HPLC)

mp

204-208 °C (lit.)

solubility

ethanol: 20 mg/mL, clear to hazy, orange to very deep orange

SMILES string

Oc1ccc(cc1)\N=N\c2ccccc2C(O)=O

InChI

1S/C13H10N2O3/c16-10-7-5-9(6-8-10)14-15-12-4-2-1-3-11(12)13(17)18/h1-8,16H,(H,17,18)/b15-14+

InChI key

DWQOTEPNRWVUDA-CCEZHUSRSA-N

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Application

2-(4-Hydroxyphenylazo)benzoic acid may be used in the preparation of:
  • 2-((4-(3,4-dicyanophenoxy)phenyl)diazenyl)benzoic acid
  • 2,2′-((((4,5-dicyano-1,2-phenylene)bis(oxy))bis(4,1-phenylene))bis(diazene-2,1-diyl)) dibenzoic acid
  • a multifunctional benzoxazine monomer

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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New water soluble phenoxy phenyl diazenyl benzoic acid substituted phthalocyanine derivatives: Synthesis, antioxidant activities, atypical aggregation behavior and electronic properties.
Agirtas MS, et al.
Dyes and Pigments, 99(2), 423-431 (2013)
Multifunctional polybenzoxazine nanocomposites containing photoresponsive azobenzene units, catalytic carboxylic acid groups, and pyrene units capable of dispersing carbon nanotubes.
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Royal Society of Chemistry Advances, 5(56), 45201-45212 (2015)
Joan-Antoni Farrera et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(7), 2277-2285 (2007-12-29)
The tautomeric equilibria of 2-(4'-hydroxyphenylazo)benzoic acid (HABA) and 2-(3',5'-dimethyl-4'-hydroxyphenylazo)benzoic acid (3',5'-dimethyl-HABA) have been studied by a combination of spectroscopic and computational methods. For neutral HABA in solvents of different polarity (toluene, chloroform, DMSO, DMF, butanol, and ethanol) the azo tautomer
M A Domin et al.
Rapid communications in mass spectrometry : RCM, 13(4), 222-226 (1999-03-31)
The ability to rapidly identify the taxonomic class of the wide variety of microorganisms involved in human and animal disease is becoming increasingly important, especially with the increasing development of resistance to the antibiotics which form the main defence against
Noritaka Kato et al.
The journal of physical chemistry. B, 109(42), 19604-19612 (2006-07-21)
This study reports a homogeneous and competitive fluorescence quenching immunoassay based on gold nanoparticle/polyelectrolyte (Au(NP)/PE) coated latex particles prepared by the layer-by-layer (LbL) technique. First, the resonant energy transfer from a layer of fluorescent PEs to Au(NP) in LbL assembled
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