2-nitronaphthalene
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 2-nitronaphthalene | |||||||||||||||
other names |
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Molecular formula | C 10 H 7 NO 2 | |||||||||||||||
Brief description |
colorless solid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 173.17 g mol −1 | |||||||||||||||
Physical state |
firmly |
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density |
1.31 g cm −3 |
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Melting point |
78.7 ° C |
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boiling point |
165 ° C (20 mbar) |
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solubility |
practically insoluble in water (22 mg / l) |
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safety instructions | ||||||||||||||||
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MAK |
Switzerland: 0.035 ml m −3 or 0.25 mg m −3 |
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2-Nitronaphthalene is a chemical compound from the group of aromatic nitro compounds . It is a colorless solid.
Occurrence
2-Nitronaphthalene occurs in low concentrations in diesel engine and industrial exhaust gases, as well as in combustion residues from wood (in the case of incomplete combustion of organic material).
presentation
2-Nitronaphthalene is obtained by reacting naphthalene with nitrating acid, although it is produced as a by-product. The main product is 1-nitronaphthalene . In industrial processes, the product ratio is> 95% (1-nitronaphthalene) to <4.5% (2-nitronaphthalene).
use
2-Nitronaphthalene is used in the manufacture of naphthylamines (for example 2-naphthylamine ), dyes and pesticides .
safety instructions
2-Nitronaphthalene dusts can form explosive mixtures with air. In animal experiments, 2-nitronaphthalene is weak, but clearly carcinogenic.
Individual evidence
- ↑ a b c d e f g Entry on 2-nitronaphthalene in the GESTIS substance database of the IFA , accessed on February 1, 2016(JavaScript required) .
- ↑ Entry on 2-nitronaphthalene in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers and / or distributors can expand the harmonized classification and labeling .
- ↑ Swiss Accident Insurance Fund (Suva): Limit values - current MAK and BAT values (search for 581-89-5 or 2-nitronaphthalene ), accessed on November 2, 2015.
- ↑ a b Laboratory for Environmental Analyzes Bremen: Occupational and Environmental Medical Analyzes ( Memento from August 29, 2013 in the Internet Archive ) (PDF; 498 kB), accessed on March 29, 2013.
- ↑ IARC (Ed.): Diesel and gasoline engine exhausts and some nitroarenes (= IARC monographs on the evaluation of carcinogenic risks to humans . Volume 46 ). IARC, Lyon, France 1989, ISBN 92-832-1246-0 ( iarc.fr [PDF]).
- ^ Health Council of the Netherlands (Ed.): 2-Nitronaphthalene: health-based calculated occupational cancer risk values . Health Council of the Netherlands, Dutch Expert Committee on Occupational Standards, Den Haag 2005, ISBN 90-5549-561-1 ( 2-Nitronaphthalene: health-based calculated occupational cancer risk values ( Memento of December 7, 2015 in the Internet Archive ) [ PDF]).
- ↑ Patent application DE2622313A1 : Process for the production of mononitro aromatics. Published on December 1, 1977 , inventor: K.-W. Thiem, A. Hamers, J. Heinen.