With a typical batch process, the toluene is fed into the nitrator and cooled to about 25 °C. Toluene is a liquid, which is colorless, water-insoluble and smells like paint thinners. Toluene's toxic effects are similar to those of benzene, although more mental status changes are seen. As toluene is an aromatic compound, it is less susceptible towards oxidation reaction. remove sources of ignition).Move victim to fresh air. Call a Poison Centre or doctor if the victim feels unwell. The boiling point of toluene is about 111 o C. It is a highly flammable liquid compound. Skin Contact: Avoid direct contact.Wear chemical protective clothing if necessary.
111 °C Alfa Aesar: 232 F (111.1111 °C) NIOSH XS5250000 110.6 °C OU Chemical Safety Data (No longer updated) More details: 111 °C Alfa Aesar L10967, 43061, 19376, 19399, 22903, 31755, 41464, 41841, 47136: 110-111 °C Oakwood 035922, 046885: 111 °C LabNetwork LN00162826: 14.5 °C / 14.56 mmHg (124.0448 °C / 760 mmHg) FooDB FDB012454 231-233 F / 760 mmHg (110.5556-111.6667 °C / 760 … Properties of Toluene. Inhalation: Take precautions to prevent a fire (e.g. The oxidation of toluene forms benzaldehyde which can further be oxidized to form benzoic acid. Mononitrotoluenes can be produced by either a batch or continuous process. Toluene is highly reactive due to the presence of methyl group.
Ph Eur - Find MSDS or SDS, a COA, data sheets and more information. Toluene is a major constituent of the glue used by paint huffers and has thus been implicated as the chemical responsible for the neurotoxic syndrome seen in this group of solvent abusers. Toluene CAS 108-88-3 for analysis EMSURE® ACS,ISO,Reag. Toluene is more reactive to electrophiles than the benzene. Toluene is considered as a benzene derivative. Toluene is a common component in gasoline, glues, and paint products. See Also: Toxicological Abbreviations Toluene (EHC 52, 1986) Toluene (WHO Food Additives Series 16) TOLUENE (JECFA Evaluation) Toluene (IARC Summary & Evaluation, Volume 71, 1999) The methyl group of toluene is a side chain in the aromatic ring structure and is oxidized to the carboxyl group in the presence of a strong oxidizing agent.
It can undergo electrophilic aromatic substitution reactions. It is a mono-substituted colorless liquid, consisting of a CH 3 group that is attached to a phenyl group.