H5126
2-(4-Hydroxyphenylazo)benzoic acid
≥90% (HPLC)
Synonym(s):
2-(4′-Hydroxybenzeneazo)benzoic acid, 4′-Hydroxyazobenzene-2-carboxylic acid, HABA, HBABA
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
HOC6H4N=NC6H4CO2H
CAS Number:
Molecular Weight:
242.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-655-2
Beilstein/REAXYS Number:
1842696
MDL number:
Assay:
≥90% (HPLC)
Quality Level
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
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
Still not finding the right product?
Explore all of our products under 2-(4-Hydroxyphenylazo)benzoic acid
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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.
Mohamed MG, et al.
Royal Society of Chemistry Advances, 5(56), 45201-45212 (2015)
Kai Qi et al.
Journal of the American Chemical Society, 126(21), 6599-6607 (2004-05-27)
Shell cross-linked nanoparticles (SCKs) presenting surface- and bioavailable biotin functional groups were synthesized via a mixed micelle methodology, whereby co-micellization of chain terminal biotinylated poly(acrylic acid)-b-poly(methyl acrylate) (PAA-b-PMA) and nonbiotinylated PAA-b-PMA were cross-linked in an intramicellar fashion within the shell
Global Trade Item Number
| SKU | GTIN |
|---|---|
| H5126-5G | 04061832109053 |
| H5126-1G | 04061825773001 |
| H5126-25G | 04061833797181 |