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2-(4-Hydroxyphenylazo)benzoic acid

matrix substance for MALDI-MS, ≥99.5%

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:
Molecular Weight:
242.23
Beilstein:
1842696
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

matrix substance for MALDI-MS

Quality Level

Assay

≥99.5% (HPLC)
≥99.5%

analyte functional class(es)

polymers

analyte chemical class(es)

glycans, peptides, proteins

technique(s)

MALDI-MS: suitable

mp

204-208 °C (lit.)
204-208 °C

solubility

ethanol: 20 mg/mL, clear

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤50 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤100 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

absorption

≥2000 at 337 nm (mol. absorption)

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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General description

2-(4-Hydroxyphenylazo)benzoic acid) (HABA), can be used for desorption of proteins, peptides and glycoproteins, thereby making it very advantageous for matrix-assisted laser desorption ionization mass spectrometry.

related product

Product No.
Description
Pricing

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

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Matrix-assisted laser desorption ionization mass spectrometry with 2-(4-hydroxyphenylazo) benzoic acid matrix.
Juhasz, Peter, Catherine E. Costello, and Klaus Biemann.
Journal of the American Society For Mass Spectrometry, 4 (5), 399-409 (1993)
K J Welham et al.
Rapid communications in mass spectrometry : RCM, 12(4), 176-180 (1998-03-11)
A variety of gram-positive and gram-negative intact bacterial cells have been analysed by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) and shown to provide fingerprint mass spectra with discrete peaks being observed over the mass range from 3 to 40 kDa.
Kenneth Kam-Wing Lo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(5), 1500-1512 (2005-11-24)
Six luminescent cyclometalated iridium(III)-dipyridoquinoxaline and -dipyridophenazine complexes [Ir(ppy)2(N-N)](PF6) (Hppy = 2-phenylpyridine; N-N = dipyrido[3,2-f:2',3'-h]quinoxaline, dpq (1); 2-n-butylamidodipyrido[3,2-f:2',3'-h]quinoxaline, dpqa (2); 2-((2-biotinamido)ethyl)amidodipyrido[3,2-f:2',3'-h]quinoxaline, dpqB (3); dipyrido[3,2-a:2',3'-c]phenazine, dppz (4); benzo[i]dipyrido[3,2-a:2',3'-c]phenazine, dppn (5); 11-((2-biotinamido)ethyl)amidodipyrido[3,2-a:2',3'-c]phenazine, dppzB (6)) have been designed as luminescent intercalators for DNA and
Kenneth Kam-Wing Lo et al.
Inorganic chemistry, 43(17), 5275-5282 (2004-08-18)
Two luminescent ruthenium(II) polypyridine complexes containing a biotin moiety [Ru(bpy)(2)(L1)](PF(6))(2) (1) and [Ru(bpy)(2)(L2)](PF(6))(2) (2) (bpy = 2,2'-bipyridine; L1 = 4-(N-((2-biotinamido)ethyl)amido)-4'-methyl-2,2'-bipyridine; L2 = 4-(N-((6-biotinamido)hexyl)amido)-4'-methyl-2,2'-bipyridine) have been synthesized and characterized, and their photophysical and electrochemical properties have been studied. Upon photoexcitation, complexes
Xiaoze Jiang et al.
Bioconjugate chemistry, 20(5), 994-1001 (2009-05-01)
Quantum dots (QDs) containing surface carboxylic groups have been successfully modified using biotinylated glycopolymer and carbohydrate/biotin reagents via EDC coupling. The biotinylated glycopolymer was synthesized in controlled dimension via the reversible addition-fragmentation chain transfer (RAFT) polymerization of the three monomers

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