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2-(4-Hydroxyphenylazo)benzoic acid (HABA) is an azo compound characterized by the presence of an azobenzene structure, where one phenyl group is substituted at position 4 by a hydroxy group, and the other phenyl group is substituted at position 2 by a carboxy group. It is known for its light yellow to orange powder appearance and is utilized in various applications due to its unique chemical properties.

1634-82-8

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1634-82-8 Usage

Uses

Used in Mass Spectrometry:
2-(4-Hydroxyphenylazo)benzoic acid is used as a matrix in matrix-assisted laser desorption/ionization (MALDI) mass spectrometry for the desorption of proteins, peptides, and glycoproteins. Its application in this field is advantageous as it aids in the ionization process, enhancing the efficiency and accuracy of mass spectrometry analysis.
Used in Chemical Synthesis:
HABA serves as a key intermediate in the preparation of various complex organic compounds, such as 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, and multifunctional benzoxazine monomers. These compounds find applications in different industries, including pharmaceuticals, materials science, and chemical research.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(4-Hydroxyphenylazo)benzoic acid is used as a building block for the synthesis of various drug candidates. Its unique structure and reactivity make it a valuable component in the development of new medications with potential therapeutic applications.
Used in Materials Science:
In materials science, HABA is utilized in the synthesis of novel materials with specific properties, such as benzoxazine monomers. These monomers can be polymerized to form high-performance polymers with applications in various industries, including electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 1634-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1634-82:
(6*1)+(5*6)+(4*3)+(3*4)+(2*8)+(1*2)=78
78 % 10 = 8
So 1634-82-8 is a valid CAS Registry Number.
InChI:InChI=1/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+

1634-82-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A10333)  2-(4-Hydroxyphenylazo)benzoic acid, 98+%   

  • 1634-82-8

  • 10g

  • 226.0CNY

  • Detail
  • Alfa Aesar

  • (A10333)  2-(4-Hydroxyphenylazo)benzoic acid, 98+%   

  • 1634-82-8

  • 50g

  • 585.0CNY

  • Detail
  • Alfa Aesar

  • (A10333)  2-(4-Hydroxyphenylazo)benzoic acid, 98+%   

  • 1634-82-8

  • 250g

  • 2412.0CNY

  • Detail
  • Sigma-Aldrich

  • (54793)  2-(4-Hydroxyphenylazo)benzoicacid  matrix substance for MALDI-MS, ≥99.5%

  • 1634-82-8

  • 54793-1G-F

  • 456.30CNY

  • Detail
  • Sigma-Aldrich

  • (54793)  2-(4-Hydroxyphenylazo)benzoicacid  matrix substance for MALDI-MS, ≥99.5%

  • 1634-82-8

  • 54793-5G-F

  • 1,790.10CNY

  • Detail
  • Aldrich

  • (H5126)  2-(4-Hydroxyphenylazo)benzoicacid  ≥98% (TLC)

  • 1634-82-8

  • H5126-1G

  • 161.46CNY

  • Detail
  • Aldrich

  • (H5126)  2-(4-Hydroxyphenylazo)benzoicacid  ≥98% (TLC)

  • 1634-82-8

  • H5126-5G

  • 285.48CNY

  • Detail
  • Aldrich

  • (H5126)  2-(4-Hydroxyphenylazo)benzoicacid  ≥98% (TLC)

  • 1634-82-8

  • H5126-25G

  • 861.12CNY

  • Detail

1634-82-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxyphenylazo)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 2-[(4-hydroxyphenyl)azo]-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1634-82-8 SDS

1634-82-8Related news

Matrix-assisted laser desorption ionization mass spectrometry with 2-(4-hydroxyphenylazo)benzoic acid matrix07/29/2019

A novel matrix substance, 2-(4-hydroxyphenylazo)benzoic acid, or HABA, has been found to be very advantageous for matrix-assisted ultraviolet laser desorption ionization mass spectrometry. This compound has been successfully used for the desorption of peptides, proteins, and glycoproteins up to ...detailed

Molecular and crystal structures of two matrices for MALDI-TOF-MS: 2-(4-hydroxyphenylazo)benzoic acid and 3,5-dimethoxy-4-hydroxycinnamic acid07/25/2019

2-(4-Hydroxyphenylazo)benzoic acid (1) and 3,5-dimethoxy-4-hydroxycinnamic acid (2) (also known as sinapinic acid), two matrices for the research of matrix-assisted laser desorption/ionization time-of-flight mass spectrum (MALDI-TOF-MS), have been structurally elucidated in this paper. The forme...detailed

Determination of structural, spectrometric and nonlinear optical features of 2-(4-hydroxyphenylazo)benzoic acid by experimental techniques and quantum chemical calculations07/24/2019

The optimized geometrical structure, vibrational and electronic transitions, chemical shifts and nonlinear optical properties of 2-(4-hydroxyphenylazo)benzoic acid (HABA) compound were presented in this study. The ground state geometrical structure and vibrational wavenumbers were carried out by...detailed

1634-82-8Relevant academic research and scientific papers

Synthesis and electrooptical properties of metal-containing azopolymers. The influence of steric factors on the electro-optical effect in polycomplexes of azobenzene derivatives with cobalt

Savchenko, Irina,Davidenko, Nikolaj,Davidenko, Irina,Popenaka, Anatolij,Syromyatnikov, Vladimir

experimental part, p. 254/[1002]-262/[1010] (2009/10/11)

We propose new structures of metal-containing azopolymers with changeable electro-optical properties in consequence of different coordination metal ions. The new monomers - 4-methacroyloxy-(4'-carboxy-3'-hydroxy)-azobenzene, 4-methacroyloxy-2'-carboxy-azobenzene and their complexes with Co and polymers based of these ones are synthesized. The influence of the electric field on the absorption spectra of new metal-containing azopolymers films are investigated. Electro-optical properties of polymeric films is determined by the re-orientation of dipole moments of azobenzene groups photo induced by polarized light in the electric field. Increase of structural inflexibility by the photo isomerization of azobenzene groups decrease the electro-optical effect value.

Azobenzene derivatives as labeling agents and intermediates thereof

-

, (2008/06/13)

A compound of the formula I: wherein R is H or —N═N-2-carboxyphenyl; A is (CH2)nor —CH═CH—, wherein n is an integer from 0 to 10, or A may also be —CH(COOH)— when R is —N═N-2-carboxyphenyl; and X is a radical selected from the group consisting of: (i) Cl; (ii) COOR1, wherein R1is p-nitrophenyl or N-succinimidyl; (iii) CONH—NHR2, wherein R2is H, COO(t-butyl) or COObenzyl; (iv) CONH—[B]—NHR3, wherein R3is H, COOR1, or CO—[B′]—maleimido, wherein R1is t-butyl, p-nitrophenyl or N-succinimidyl, and B and B′, the same or different, are (CH2)nwherein n is an integer from 2 to 10; (v) CONH—[B]—COOR4, wherein R4is H, C1-C8alkyl, N-succinimidyl; (vi) CONH—[B]—OH; (vii) CONH—[B]—CONH—NHR2, wherein R2is H, COO(t-butyl) or COObenzyl; and (viii) NHR2, wherein R2is H, COO(t-butyl) or COObenzyl, when A is —CH(COOH)— and R is —N═N-2-carboxyphenyl. The 4′-hydroxyazobenzene-2-carboxylic acid (HABA) compounds are novel reagents for labeling, isolation and detection of biological molecules.

Low excitation energy band of 4-hydroxyazobenzene derivatives

Mahmoud, M. R.,Ibrahim, S. A.,Hamed, M. A.

, p. 729 - 734 (2007/10/02)

The low excitation energy band appeared in the electronic spectra of some 4-hydroxyazobenzene derivatives is assigned to an electronic transition of the type η-?*.It is concluded that 4-hydroxyazobenzene derivatives exist mainly in the true azo form.On the other hand, the visible spectra of the azo compound; 4-hydroxy-2-carboxyazobenzene is interpreted on the basis that this compound exists in a tautomeric equilibrium of the type azo hydrazone, originating from the carboxyl group at the ortho position to the azo one.

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