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104-23-4

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104-23-4 Usage

Uses

4''-Aminoazobenzene-4-sulphonic Acid can be used in photocatalytic wastewater treatment

Preparation

4-(Phenyldiazenyl)benzenamine?sulfonated.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 104-23-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104-23:
(5*1)+(4*0)+(3*4)+(2*2)+(1*3)=24
24 % 10 = 4
So 104-23-4 is a valid CAS Registry Number.

104-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((4-aminophenyl)diazenyl)benzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 4-[(4-aminophenyl)diazenyl]benzenesulfonic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:104-23-4 SDS

104-23-4Synthetic route

sodium anilinomethanesulfonate
26021-90-9

sodium anilinomethanesulfonate

p-sulfobenzenediazonium chloride
6118-33-8

p-sulfobenzenediazonium chloride

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
Stage #1: sodium anilinomethanesulfonate; p-sulfobenzenediazonium chloride With sodium acetate In water
Stage #2: With sodium hydroxide In water Reflux;
70%
phenyl toluenesulfonamide
68-34-8

phenyl toluenesulfonamide

4-diazobenzenesulfonic acid
305-80-6

4-diazobenzenesulfonic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
und Verseifen des Reaktionsprodukts mit konz.Schwefelsaeure bei 40grad;
4-(4-nitro-phenylazo)-benzenesulfonic acid
23792-61-2

4-(4-nitro-phenylazo)-benzenesulfonic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With ammonium hydrosulphide; ethanol
4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid
861869-60-5

4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

2,4,6-Trinitrophenol
88-89-1

2,4,6-Trinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-phenylazoaniline hydrochloride
3457-98-5

4-phenylazoaniline hydrochloride

A

4-aminoazobenzene-3,4'-disulfonic acid
101-50-8

4-aminoazobenzene-3,4'-disulfonic acid

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With sulfuric acid at 90 - 100℃;
With sulfuric acid at 90 - 100℃;
4-diazobenzenesulfonic acid
305-80-6

4-diazobenzenesulfonic acid

aniline
62-53-3

aniline

A

Phenyl azide
622-37-7

Phenyl azide

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

4-diazobenzenesulfonic acid
305-80-6

4-diazobenzenesulfonic acid

aniline
62-53-3

aniline

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With water man laesst 24 Stdn.stehen, filtriert ab und entzieht dem Nied. durch kal. Aether beigemengtes Diazoaminobenzol; die ungeloeste 4'-Amino-azobenzol-sulfonsaeure-(4) bindet man an Ammoniak und reinigt das Salz durch Umkrystallis.;
sulfate of 4-amino-azobenzene

sulfate of 4-amino-azobenzene

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With sulfuric acid; sulfur trioxide at 30 - 35℃;
With sulfuric acid; sulfur trioxide at 30 - 35℃;
sulfuric acid
7664-93-9

sulfuric acid

aniline yellow
60-09-3

aniline yellow

A

4-aminoazobenzene-3,4'-disulfonic acid
101-50-8

4-aminoazobenzene-3,4'-disulfonic acid

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
at 30 - 35℃;
at 30 - 35℃;
sulfate of 4-amino-azobenzene

sulfate of 4-amino-azobenzene

A

4-aminoazobenzene-3,4'-disulfonic acid
101-50-8

4-aminoazobenzene-3,4'-disulfonic acid

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With sulfuric acid; sulfur trioxide at 30 - 35℃;
sulfuric acid
7664-93-9

sulfuric acid

aniline yellow
60-09-3

aniline yellow

A

2-amino-5-(4-sulfo-phenylazo)-benzene-1,3-disulfonic acid

2-amino-5-(4-sulfo-phenylazo)-benzene-1,3-disulfonic acid

B

4-aminoazobenzene-3,4'-disulfonic acid
101-50-8

4-aminoazobenzene-3,4'-disulfonic acid

C

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
at 70℃;
at 70℃;
ethanol
64-17-5

ethanol

4-(4-nitro-phenylazo)-benzenesulfonic acid
23792-61-2

4-(4-nitro-phenylazo)-benzenesulfonic acid

ammonium hydrosulfide

ammonium hydrosulfide

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-diazobenzenesulfonic acid
305-80-6

4-diazobenzenesulfonic acid

water
7732-18-5

water

aniline hydrochloride
142-04-1

aniline hydrochloride

A

benzene diazonium chloride
100-34-5

benzene diazonium chloride

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

4-diazobenzenesulfonic acid
305-80-6

4-diazobenzenesulfonic acid

water
7732-18-5

water

aniline
62-53-3

aniline

A

aniline yellow
60-09-3

aniline yellow

B

Phenyl azide
622-37-7

Phenyl azide

C

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

D

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

hydrogenchloride
7647-01-0

hydrogenchloride

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid
25739-61-1

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid

A

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

hydrogenchloride
7647-01-0

hydrogenchloride

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid ; potassium-compound

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid ; potassium-compound

A

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

hydrogenchloride
7647-01-0

hydrogenchloride

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid ; sodium-compound

4-[4-(2,4-dinitro-anilino)-phenylazo]-benzenesulfonic acid ; sodium-compound

A

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid
861869-60-5

4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid

water
7732-18-5

water

A

2,4,6-Trinitrophenol
88-89-1

2,4,6-Trinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid
861869-60-5

4-[4-(2,4,6-trinitro-anilino)-phenylazo]-benzenesulfonic acid

KOH-solution

KOH-solution

A

2,4,6-Trinitrophenol
88-89-1

2,4,6-Trinitrophenol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-[4-(2-hydroxy-[1]naphthylazo)-phenylazo]-benzenesulfonic acid
37678-79-8

4-[4-(2-hydroxy-[1]naphthylazo)-phenylazo]-benzenesulfonic acid

sodium amalgam

sodium amalgam

A

1-amino-2-naphthol
2834-92-6

1-amino-2-naphthol

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

methyl orange
502-02-3

methyl orange

A

C14H13N3O4S

C14H13N3O4S

B

C14H19N3O7S

C14H19N3O7S

C

4-hydrazino-2-hydroxy-benzenesulfonic acid

4-hydrazino-2-hydroxy-benzenesulfonic acid

D

4-(4-methylamino-phenylazo)-benzenesulfonic acid
5713-92-8

4-(4-methylamino-phenylazo)-benzenesulfonic acid

E

4-phenylazo-benzenesulfonic acid
2484-88-0

4-phenylazo-benzenesulfonic acid

F

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
With 1% Pt-CaCu3Ti4O12; water; oxygen for 11h; Quantum yield; Time; Reagent/catalyst; Wavelength; Visible light irradiation;
methyl orange
547-58-0

methyl orange

A

4-(4-methylamino-phenylazo)-benzenesulfonic acid
5713-92-8

4-(4-methylamino-phenylazo)-benzenesulfonic acid

B

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
In water pH=2; Kinetics; pH-value; Sonolysis; Photolysis;
aniline
62-53-3

aniline

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: sodium hydrogensulfite / water / 1 h / 65 °C
1.2: 2.25 h / 65 °C
2.1: sodium acetate / water
2.2: Reflux
View Scheme
3,5-bis(methoxycarbonyl)benzoic acid
38588-64-6

3,5-bis(methoxycarbonyl)benzoic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-((4-(3,5-bis(methoxycarbonyl)benzamido)phenyl)diazenyl)benzenesulfonic acid

4-((4-(3,5-bis(methoxycarbonyl)benzamido)phenyl)diazenyl)benzenesulfonic acid

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 115℃; for 4h; Inert atmosphere;98%
5-((4-(phenyldiazenyl)phenyl)carbamoyl)isophthalic acid

5-((4-(phenyldiazenyl)phenyl)carbamoyl)isophthalic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C45H33N9O9S2

C45H33N9O9S2

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 115℃; for 6h; Inert atmosphere;93%
C23H18N2O6

C23H18N2O6

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C47H36N8O10S2

C47H36N8O10S2

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 75 - 115℃; for 6.5h; Inert atmosphere;86%
C16H11NO7

C16H11NO7

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C52H38N10O13S3

C52H38N10O13S3

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 75 - 115℃; for 5.5h; Inert atmosphere;86%
benzene-1,3,5-tricarboxylic acid
554-95-0

benzene-1,3,5-tricarboxylic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C45H33N9O12S3

C45H33N9O12S3

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 75 - 115℃; for 4.5h; Inert atmosphere;85%
C16H13NO5

C16H13NO5

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C40H31N7O9S2

C40H31N7O9S2

Conditions
ConditionsYield
With pyridine; triphenyl phosphite In N,N-dimethyl acetamide at 75 - 115℃; for 6.5h; Inert atmosphere;84%
C21H14N4O7

C21H14N4O7

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

C45H32N10O11S2

C45H32N10O11S2

Conditions
ConditionsYield
Stage #1: C21H14N4O7 With oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; for 4h;
Stage #2: 4'-aminoazobenzene-4-sulfonic acid With triethylamine In dichloromethane; N,N-dimethyl-d6-formamide at 0℃; for 40h;
60%
diethyl ether
60-29-7

diethyl ether

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

A

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester
111915-50-5

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester

B

methyl orange
547-58-0

methyl orange

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester
111915-50-5

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester

Conditions
ConditionsYield
With diethyl ether
4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

A

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester
111915-50-5

4-(4-dimethylamino-phenylazo)-benzenesulfonic acid methyl ester

B

methyl orange
502-02-3

methyl orange

Conditions
ConditionsYield
With diethyl ether
7-(furan-2-carbonylamino)-4-hydroxy-naphthalene-2-sulfonic acid
109258-06-2

7-(furan-2-carbonylamino)-4-hydroxy-naphthalene-2-sulfonic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

7-(furan-2-carbonylamino)-4-hydroxy-3-[4-(4-sulfo-phenylazo)-phenylazo]-naphthalene-2-sulfonic acid

7-(furan-2-carbonylamino)-4-hydroxy-3-[4-(4-sulfo-phenylazo)-phenylazo]-naphthalene-2-sulfonic acid

Conditions
ConditionsYield
With sodium hydroxide; sodium carbonate
7-hydroxy-naphthalene-1-sulfonic acid
132-57-0

7-hydroxy-naphthalene-1-sulfonic acid

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

7-hydroxy-8-[4-(4-sulfo-phenylazo)-phenylazo]-naphthalene-1-sulfonic acid

7-hydroxy-8-[4-(4-sulfo-phenylazo)-phenylazo]-naphthalene-1-sulfonic acid

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite
4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-(4-sulfo-phenylazo)-benzenediazonium-betaine
65036-56-8

4-(4-sulfo-phenylazo)-benzenediazonium-betaine

Conditions
ConditionsYield
With mixture of gaseous nitrogen oxides; water
4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-aminoazobenzene-3,4'-disulfonic acid
101-50-8

4-aminoazobenzene-3,4'-disulfonic acid

Conditions
ConditionsYield
With sulfuric acid at 100℃;
4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

A

1,4-phenylenediamine
106-50-3

1,4-phenylenediamine

B

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

Conditions
ConditionsYield
With hydrogenchloride; tin
4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

4-[(4-hydroxy)phenylazo]benzenesulfonic acid
2918-83-4

4-[(4-hydroxy)phenylazo]benzenesulfonic acid

Conditions
ConditionsYield
With cis-nitrous acid und Kochen der gebildeten Diazoverbindung mit Wasser;
hydrogenchloride
7647-01-0

hydrogenchloride

4'-aminoazobenzene-4-sulfonic acid
104-23-4

4'-aminoazobenzene-4-sulfonic acid

tin

tin

A

1,4-phenylenediamine
106-50-3

1,4-phenylenediamine

B

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

104-23-4Relevant articles and documents

Rapid and direct spectrophotometric method for kinetics studies and routine assay of peroxidase based on aniline diazo substrates

Mirazizi, Fatemeh,Bahrami, Azita,Haghbeen, Kamahldin,Shahbani Zahiri, Hossein,Bakavoli, Mehdi,Legge, Raymond L.

, p. 1162 - 1169 (2016)

Peroxidases are ubiquitous enzymes that play an important role in living organisms. Current spectrophotometrically based peroxidase assay methods are based on the production of chromophoric substances at the end of the enzymatic reaction. The ambiguity regarding the formation and identity of the final chromophoric product and its possible reactions with other molecules have raised concerns about the accuracy of these methods. This can be of serious concern in inhibition studies. A novel spectrophotometric assay for peroxidase, based on direct measurement of a soluble aniline diazo substrate, is introduced. In addition to the routine assays, this method can be used in comprehensive kinetics studies. 4-[(4-Sulfophenyl)azo]aniline (λ max = 390 nm, ? = 32 880 M?1 cm?1 at pH 4.5 to 9) was introduced for routine assay of peroxidase. This compound is commercially available and is indexed as a food dye. Using this method, a detection limit of 0.05 nmol mL?1 was achieved for peroxidase.

The mechanism of sonophotocatalytic degradation of methyl orange and its products in aqueous solutions

He, Yuanhua,Grieser, Franz,Ashokkumar, Muthupandian

, p. 974 - 980 (2011)

In this study, it was found that a hybrid technique, sonophotocatalysis, is able to degrade a parent organic pollutant (methyl orange) as well as its by-products. The analysis of products formed during the whole degradation has demonstrated that the pH or the selection of oxidation process (sonolysis/photocatalysis/sonophotocatalysis) is able to control the degradation pathway. It was shown in the by-products analysis that the solution pH can alter the amount of each product generated during the sonophotocatalytic degradation. It was revealed that the different degradation rates of methyl orange and its products result from the solution pH and the nature of the organic products. Furthermore, a comparison of the data obtained from the oxidation processes on the degradation of the reaction intermediates identified the advantages of the combined system. It is concluded that sonophotocatalysis is capable of yielding a more complete and faster mineralization of organic pollutants than the individual processes. However, as in the degradation of the parent compound, the overall mineralization is lower than an additive effect (negative synergistic effect).

Preparation of aminoazo dyes

-

, (2008/06/13)

Aminoazo dyes are prepared from the corresponding N-sulfomethylated aminoazo dyes by aqueous acid hydrolysis in the presence of amidosulfuric acid, urea or mixtures thereof.

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