Phenyl isocyanate
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Phenyl isocyanate | |||||||||||||||
other names |
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Molecular formula | C 7 H 5 NO | |||||||||||||||
Brief description |
clear, colorless and tear-irritating liquid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 119.12 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
1.10 g cm −3 |
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Melting point |
−31 ° C |
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boiling point |
166 ° C |
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Vapor pressure |
2.63 mbar (20 ° C) |
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solubility |
Decomposes in water |
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Refractive index |
1.535 (20 ° C) |
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safety instructions | ||||||||||||||||
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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 . Refractive index: Na-D line , 20 ° C |
Phenyl isocyanate is a chemical compound from the group of organic isocyanates .
Extraction and presentation
Phenyl isocyanate can be obtained from aniline and phosgene , with more than 1000 t per year being manufactured or imported.
properties
Phenyl isocyanate is a tear-irritating, inflammable, colorless to yellowish liquid with a pungent odor. In water , it hydrolyzes to aniline with carbon dioxide being split off. The heat of decomposition determined by DSC is −49 kJ · mol −1 or −410 kJ · kg −1 .
use
Phenyl isocyanate is used as a reagent for amines and alcohols, for the production of pharmaceuticals, pesticides (e.g. carbetamide ), textile auxiliaries (optical brighteners), plasticizers and in the paint and photo industry.
safety instructions
The vapors of phenyl isocyanate can form an explosive mixture with air ( flash point 51 ° C, ignition temperature 580 ° C).
Individual evidence
- ↑ Entry on phenyl isocyanate. In: Römpp Online . Georg Thieme Verlag, accessed on June 16, 2014.
- ↑ a b c d e f g h i j Entry on phenyl isocyanate in the GESTIS substance database of the IFA , accessed on January 9, 2019(JavaScript required) .
- ↑ Phenyl isocyanate data sheet from Sigma-Aldrich , accessed on May 14, 2017 ( PDF ).
- ↑ a b Toxicological assessment of phenyl isocyanate (PDF) at the professional association raw materials and chemical industry (BG RCI), accessed on August 22, 2012.
- ↑ T. Grewer, O. Klais: Exothermic decomposition - investigations of the characteristic material properties. (= Humanization of working life. Volume 84). VDI-Verlag, Düsseldorf 1988, ISBN 3-18-400855-X , p. 9.