o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
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OECD SIDS o-<strong>TOLUIDINE</strong><br />
methylene-bis-2-methylcyclohexylamine, fungicide intermediates such as 2-amino-4-methylbenzothiazole,<br />
o-fluorobenzoyl chloride, and some pharmaceutical intermediates (Bowers, 2002).<br />
o-Toluidine is also used for the photometric determination of glucose in blood (Roempp, 1999).<br />
No direct consumer use is known for o-toluidine (Bayer <strong>Chemicals</strong>, 2004). o-Toluidine is contained<br />
in products listed in the Danish, Finnish, Norwegian, and Swedish Product Registers (SPIN, 2004).<br />
No consumer application is registered. In the Finnish Product Register there is a confidential listing<br />
that o-toluidine is used for the manufacture of rubber and plastic products as a vulcanizer and for<br />
other use. For the Danish Product Register there is a listing as a process regulator in 2000 and 2001<br />
(the latest year of reporting). According to this register, in total “0.0 tonnes” of o-toluidine were<br />
used in 2001, signifying that o-toluidine is not added intentionally into these processes.<br />
The Swiss Product Register (2004) lists 2 public products (analytical kits), both with an o-toluidine<br />
concentration of about 0.1 %. Although both analytical kits are listed as public products, it is<br />
assumed that these products are used industrially. Another similar product, an analytical substance,<br />
is registered for industrial use with an o-toluidine content of less than 1 %. There are about 10<br />
metallic mordants registered for industrial use which are probably prepared from o-toluidine but<br />
also do not contain relevant o-toluidine levels (< 0.1 %) (Swiss Product Register, 2004).<br />
2.2 Environmental Exposure and Fate<br />
2.2.1 Sources of Environmental Exposure<br />
o-Toluidine occurs in tobacco leaves, several vegetables, and black tea (cf Chapter 2.2.8). o-Toluidine<br />
is ubiquitous in the human environment because it is a major component of tobacco smoke (cf<br />
Chapters 2.2.8 and 2.3). It is a degradation intermediate of o-nitrotoluene in former ammunition<br />
sites (cf Chapter 2.2.8). Releases of o-toluidine may occur from products like coal oil, gasoline, (cf<br />
Chapter 2.2.8) and during its manufacturing and processing. Exposure of the environment due to<br />
release of synthetic o-toluidine from products is not likely to occur. The following information on<br />
environmental exposure from manufacturing and processing of o-toluidine in the Sponsor country is<br />
available:<br />
At all five sites in the Sponsor country o-toluidine is manufactured or processed in closed systems<br />
The effluent concentrations from the wastewater treatment plants of these companies are below the<br />
detection limits of 20 µg/l (production site), and below 10 µg/l (two processing sites) and below<br />
25 µg/l (one processing site) respectively (Bayer <strong>Chemicals</strong>, 2004; BASF AG, 2004; Clariant<br />
GmbH, 2005). For one production site in the Sponsor country only data for the sum of the toluidine<br />
isomers are available (BASF AG, 2005).<br />
At the Bayer production site, the exhausts from hydrogenation, distillation, and processing are<br />
connected to thermal exhaust purification plants and air washing units. In 2000, according to the<br />
current Official Emission Declaration, < 25 kg/a of o-toluidine was emitted into the atmosphere at<br />
the production and processing sites (Bayer <strong>Chemicals</strong>, 2004).<br />
At the Bayer production site, waste from the manufacturing process is incinerated in an incinerator<br />
for hazardous wastes (Bayer <strong>Chemicals</strong>, 2004).<br />
The wastewater from hydrogenation is stripped and the wastewater is led to the Leverkusen<br />
industrial and municipal wastewater treatment plant. The wastewater from processing is led to the<br />
Bayer industrial wastewater treatment plant in Brunsbuettel (Bayer <strong>Chemicals</strong>, 2004).<br />
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