Aminocarb
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Aminocarb | ||||||||||||||||||
other names |
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Molecular formula | C 11 H 16 N 2 O 2 | ||||||||||||||||||
Brief description |
colorless solid |
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properties | |||||||||||||||||||
Molar mass | 208.26 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
93-94 ° C |
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solubility |
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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 . |
Aminocarb is a chemical compound from the group of carbamates .
Extraction and presentation
Aminocarb can be obtained by reacting 4-dimethylamino-3-methylphenol with methyl isocyanate .
properties
Aminocarb is a colorless solid that is sparingly soluble in water.
use
Aminocarb is used as a non-systemic insecticide .
Individual evidence
- ↑ a b c d e f g h i Entry on aminocarb in the GESTIS substance database of the IFA , accessed on July 4, 2015(JavaScript required) .
- ^ John H. Montgomery: Agrochemicals Desk Reference . CRC Press, 1997, ISBN 978-1-4200-4921-3 , pp. 21 ( limited preview in Google Book search).
- ↑ Entry on Aminocarb 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 .
- ↑ Thomas A. Unger: Pesticide Synthesis Handbook . William Andrew, 1996, ISBN 978-0-8155-1853-2 , pp. 61 ( limited preview in Google Book search).
- ↑ TSS Dikshith: Handbook of Chemicals and Safety . CRC Press, 2010, ISBN 978-1-4398-2061-2 , pp. 76 ( limited preview in Google Book search).