materials analysis

Quantitative determination of 26 aromatic

amines derived from banned azo dyes in
textiles through the use of lC, tandem mS, and
identification of some structural isomers.

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ABSTRACT
Application Note The determination of some aromatic amines derived from banned azo
dyes is important in chemical safety control in the fashion industry. Many
European and international regulations (REACH, GB and KC Mark) strictly
Authors limit their presence. The main regulations for the identification of aromatic
amines derived from azo dyes define that analysis has to be conducted by
Dr. Dall’Anese Riccardo Giovanni, at least two chromatographic methods, in order to avoid misidentification
Dr. Bartolini Giuseppe and due to the presence of matrix interferences or structural isomers. In this
Dr. Franchi Andrea study, an analytical method has been developed that minimises matrix
clean-up and identifies the amines in an unequivocal way. This study also
Buzzi Laboratorio Analisi, allows for the efficient separation of structural isomers, avoiding the need
Prato, Italy. for double analysis.

INTRODUCTION:
Some azo dyes can produce, in specific conditions, some primary aromatic amines
(PAAs) that are considered to be carcinogenic by the most important international
authorities. For this reason, specific regulations have been introduced in order to
monitor their presence in materials used in the fashion industry, such as textiles
and leathers. The various regulations stipulate different groups of aromatic amines
with varying concentration limits. The strictest regulation in force is the Chinese
regulation GB 18401:2010 which allows for the presence of 24 aromatic amines,
with a limit of 20 mg/kg for each amine.

The main research methods for the analysis of these amines use GC/MS. In many cases, detection by gas chromatogra-
phy is complicated by the presence of polar analytes and by the separation of structural isomers that are not banned by
international regulations. Liquid chromatography allows for a reliable, efficient method that is faster than traditional gas
chromatography methods. It also allows for the efficient separation of structural isomers.
The method developed in this application note is really useful and versatile. It reliably identifies aromatic amines in many
materials, avoids expensive clean-up and is able to separate the structural isomers of interest.
ANALYTICAL TECHNIQUE
Reagents and standards Instrumentation
Acetonitrile, water, formic acid, isomers of specific amines HPLC separation was performed on the Agilent 1200
from Sigma-Aldrich (Milan, Italy). LC system using an Agilent Poroshell 120 SB-C18
column with detection on the Agilent 6420 Triple
Standard of 26 aromatic amines at 100 mg/L from Ultra
Quadrupole Mass Spectrometer.
Scientific – Analytical Standard (Bologna, Italy).

Agilent 1200/6420 LC/QQQ Operating Conditions

LC Conditions MS Conditions
Analytical Column Poroshell 120 SB-C18 3.0 x 100mm x 2.7µm Acquisition Parameters ESI Positive Ion Mode
Column Temperature 40°C Gas Temperature 320°C
Injection Volume 0.5 µL Gas Flow 10 L/min
Mobile Phase A = 0.05 mM Formic Acid in Water Nebuliser Pressure 50 psi
B = 0.1% Formic Acid in Acetonitrile Capillary Voltage 3000 V
Run Time 12 minutes
Flow Rate 0.6 mL/min
Gradient Program Time (minutes) Gradient (% A)
0 75
0.5 75
5 30
8 5

MRM Transitions – ESI Positive Ion Mode

CAS Scan Precursor Product Product Fragmentor Collision
Amine
Number Segment Ion (m/z) Ion 1 (m/z) Ion 2 (m/z) Voltage (V) Energy (V)
3,3'-Dimethoxybenzidine 119-90-4 1 245.1 230.1 213 100 15
4,4'-Methylenedi-o-
838-88-0 1 227.3 195.2 178.3 100 15
toluidine
3,3'-Dimethylbenzidine 119-93-7 1 213.0 198 181 100 15
4,4'-Oxydianiline 101-80-4 1 201.2 184.1 93.0 100 15
4,4'-Diaminodiphenyl-
101-77-9 1 199.5 106.1 89.1 100 20
methane
Benzidine 92-87-5 1 184.3 167.5 93.0 100 15
4-Methoxy-m-phenylen-
615-05-4 1 139.1 124.1 107.3 100 15
ediamine
p-Cresidine 120-71-8 1 138.1 123.4 106.1 100 15
o-Anisidine 90-04-0 1 124.1 109.2 92.2 100 15
4-Methyl-m-phenylene-
95-80-7 1 123.3 106.1 79.2 100 15
diamine
1,4-Phenylenediamine 106-50-3 1 109.2 92.2 65.1 100 15
o-Toluidine 95-53-4 1 108.3 91.1 65.2 100 15
Aniline 62-53-3 1 94.1 77.1 51.1 100 15
2,4,5-Trimethylaniline 137-17-7 1 136.3 121.3 91.2 100 15
2,4-Dimethylaniline 95-68-1 2 122.1 105.1 79.2 100 15
4,4'-Thioaniline 139-65-1 2 217.2 200.1 183.0 100 15
2-Naphthylamine 91-59-8 2 144.1 127.4 117.1 100 15

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 4-Chloroaniline 106-47-8 2 128.3 111.2 93.2 100 15
2,6-Dimethylaniline 87-62-7 2 122.1 107.1 79.2 100 15
5-Nitro-o-toluidine 99-55-8 3 153.3 107.3 90.2 100 15
p-Aminobiphenyl 92-67-1 3 170.2 153.2 128.4 100 20
4-Chloro-o-toluidine 95-69-2 3 142.1 128.2 107.1 100 15
4,4'-Methylene-bis(2-
101-14-4 4 268.2 232.2 196.1 100 20
chloroaniline)
3,3'-Dichlorobenzidine 91-94-1 4 254.2 218.1 183.0 100 15
o-Aminoazotoluene 97-56-3 4 226.1 121.1 107.1 100 15
p-Aminoazobenzene 60-09-3 4 198.1 93.1 77.1 100 15

Sample Preparation
Textiles not dyed with disperse dyes were extracted In the case of fabrics dyed with disperse dyes, samples
using the procedure in ISO 14362-1:2012, while for were initially extracted with Chlorobenzene, before
leather the procedures in ISO 17234-1:2010 and 17234- continuing with the procedures listed above. In both cases,
2:2010 were used. The organic solutions were filtered Anthracene-d10 (CAS 1719-06-8) was used as the internal
with regenerated cellulose filters before injection. standard, to give a final concentration of 10 mg/mL.

Results and Discussion

The separation of the 26 aromatic amines was achieved by optimisation of the chromatographic conditions, including
the choice of chromatographic column and optimisation of the spectrometer conditions.

Separation of Isomers
The separation of structural isomers can be extremely Amine isomer CAS number Retention time (min)
important as regards the possibility of false positives. 1-Naphthylamine 134-32-7 3.008
In many gas chromatographic separations, the elution 2-Naphthylamine 91-59-8 2.222
of specific amine isomers can differ by a few seconds. 2,4-Dimethylaniline 95-68-1 1.070
This difference can be part of the statistical variability 2,5-Dimethylaniline 95-78-3 1.275
of the retention times of each isomer. For this reason 2,6-Dimethylaniline 87-62-7 2.225
many of the regulations mention simultaneous 2,3-Dimethylaniline 87-59-2 1.095
determination using more than one chromatographic 3,4-Dimethylaniline 95-64-7 0.965
method, in order to avoid misidentifications due 3,5-Dimethylaniline 108-69-0 1.145
to the presence of structural isomers or matrix 2-Chloroaniline 95-51-2 4.430
interferences. The use of liquid chromatography limits 3-Chloroaniline 108-42-9 3.495
these difficulties allowing for the efficient and reliable 4-Chloroaniline 106-47-8 2.095
determination of each isomer. Results are shown in o-Anisidine 90-04-0 0.995
Table 1. m-Anisidine 536-90-3 0.960
p-Anisidine 104-94-9 0.760
o-Toluidine 95-53-4 1.045
m-Toluidine 108-44-1 0.920
p-Toluidine 106-49-0 0.860

Table 1: Retention times of structural isomers of some amines

used in this study.

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Calibration Curves
The calibrations were produced using the external standard method with 4 calibration points at 0.1, 0.5, 1 and 5
mg/L of amines. Linear regression was used and the curves were forced through the origin. Table 2 shows the
performance parameters for all the amines. All amines display optimal regression coefficients (R2) and detection
limits.

Amine Equation R2 Regression LOD RSD (%)

3,3'-Dimethoxybenzidine y= 29934x + 553 0.999 Linear 1.2 3.1
4,4'-Methylenedi-o-toluidine y= 1378x + 21 0.999 Linear 0.4 1.8
3,3'-Dimethylbenzidine y= 13557x + 1027 0.999 Linear 1.1 6.5
4,4'-Oxydianiline y= 2949x + 67 0.999 Linear 0.8 1.2
4,4'-Diaminodiphenylmethane y= 24505x + 693 0.999 Linear 0.8 1.2
Benzidine y= 1113x - 20 0.999 Linear 0.9 3.5
4-Methoxy-m-phenylenediamine y= 31567x + 1226 0.999 Linear 1.5 5.2
p-Cresidine y= 396223x + 8522 0.999 Linear 1.0 3.8
o-Anisidine y= 401391x + 10677 0.999 Linear 1.3 0.5
4-Methyl-m-phenylenediamine y= 55488x + 1330 0.999 Linear 3.2 1.4
1,4-Phenylenediamine y= 43230x + 1308 0.999 Linear 0.6 1.1
o-Toluidine y= 213000x + 12326 0.999 Linear 0.6 0.9
Aniline y= 26451x + 17792 0.999 Linear 0.4 1.3
2,4,5-Trimethylaniline y= 180357x + 2967 0.999 Linear 1.2 1.5
2,4-Dimethylaniline y= 207557x + 9137 0.999 Linear 1.8 4.7
4,4'-Thioaniline y= 47851x - 940 0.999 Linear 1.1 4.2
2-Naphthylamine y= 118838x + 2445 0.999 Linear 0.3 1.5
4-Chloroaniline y= 152241x - 1938 0.999 Linear 1.6 7.2
2,6-Dimethylaniline y= 77129x - 353 0.999 Linear 2.1 3.9
5-Nitro-o-toluidine y= 127200x - 51 0.999 Linear 17.2 13.5
p-Aminobiphenyl y= 86449x + 440 0.999 Linear 4.1 0.4
4-Chloro-o-toluidine y= 145693x - 1271 0.999 Linear 3.3 0.7
4,4'-Methylenebis(2-chloroaniline) y= 3311x + 75 0.999 Linear 3.1 5.5
3,3'-Dichlorobenzidine y= 5942x + 200 0.999 Linear 0.7 4.8
o-Aminoazotoluene y= 154925x + 7559 0.999 Linear 0.7 1.1
p-Aminoazobenzene y= 261090x + 10032 0.999 Linear 1.8 1.3

Table 2: Calibration curves equations, R2, LOD and % RSD for the amines used in this study.

The percentage recovery is on average greater than 85% and is calculated using the internal standard, Anthracene-d10.
Figure 1 shows a typical standard chromatogram of the 26 amines and Figure 2 shows some examples of calibration
curves.

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Figure 1: Example of a standard chromatogram.

Figure 2: Examples of amine calibration curves.

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CONCLUSIONS
This method is an extremely fast and reliable method for the determination of aromatic amines derived from azo dyes
that have been banned by international regulations. Similar results were also observed using purification with sorbent
packed columns, reducing sample preparation time. This method enables these aromatic amines to be screened and
quantitated at the same time.

REFERENCES
[1] Simultaneous determination of aliphatic and aromatic amines in [5] Quantitative determination of 22 primary aromatic amines by
ambient air and airborne particulate matters by gas chromatography- cation-exchange solid-phase extraction and liquid chromatography-
mass spectrometry, Akyüz, M., Atmospheric Environment, Volume 42, mass spectrometry, Aznar, M., Canellas, E., Nerín, C., Journal of
Issue 16, 2008, 3809-3819. Chromatography A, Volume 1216, 2009, 5176-5181.

[2] Determination of primary aromatic amines in water food simulant using [6] UNI EN 14362-1:2012, Textiles – Methods for determination
solid-phase analytical derivatization followed by gas chromatography of certain aromatic amines derived from azo colorants - Part 1:
coupled with mass spectrometry, Brede, C., Skjevrak, I., Herikstad, H., Detection of the use of certain azo colorants accessible with and
Journal of Chromatography A, Volume 983, Issues 1-2, 2003, 35-42. without extracting the fibres.

[3] Rapid and simultaneous analysis of ten aromatic amines in [7] UNI EN ISO 17234-1:2010, Leather – Chemical tests for the
mainstream cigarette smoke by liquid chromatography/electrospray determination of certain azo colorants in dyed leathers - Part 1:
ionization tandem mass spectrometry under ISO and “Health Canada Determination of certain aromatic amines derived from azo colorants.
intensive” machine smoking regimes, Xie, F., Yu, J., Wang, S., Zhao, G.,
[8] UNI EN ISO 17234-2:2011, Leather – Chemical tests for the
Xia, Q., Zhang, X., Zhang, S., Talanta, Volume 115, 2013, 435-441.
determination of certain azo colorants in dyed leathers - Part 2:
[4] Specific determination of 20 primary aromatic amines in aqueous Determination of 4-aminoazobenzene.
food simulants by liquid chromatography-electrospray ionization-tandem
[9] GB/T 17592-2011, Textiles – Determination of the banned azo
mass spectrometry, Mortensen, S. K., Trier, X. T., Foverskov, A., Petersen,
colourants.
J. H., Journal of Chromatography A, Volume 1091, Issues 1-2, 2005, 40-50.

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