Anthranilamide
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Anthranilamide | |||||||||||||||
other names |
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Molecular formula | C 7 H 8 N 2 O | |||||||||||||||
Brief description |
colorless to yellowish odorless solid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 136.15 g mol −1 | |||||||||||||||
Physical state |
firmly |
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density |
1.17 g cm −3 |
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Melting point |
111-113 ° C |
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boiling point |
300 ° C |
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solubility |
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safety instructions | ||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Anthranilamide is a chemical compound from the group of carboxamides .
Extraction and presentation
Anthranilamide can be obtained by reacting ammonia , ammonium carbonate and ammonium chloride with isatoic anhydride .
properties
Anthranilamide is a flammable, hardly inflammable, crystalline, colorless to yellowish, odorless solid that is sparingly soluble in water.
use
Anthranilamide can be used for non-selective, efficient fluorescent labeling of glycans . It is also used as an acetaldehyde scavenger in PET bottles and as an intermediate for dyes, pharmaceuticals, propellants and other chemicals. In engine lubricating oils, it prevents copper and magnesium corrosion.
Individual evidence
- ↑ a b c d e f g h i Entry on anthranilamide in the GESTIS substance database of the IFA , accessed on January 8, 2020(JavaScript required) .
- ↑ a b c d data sheet 2-aminobenzamide, 98 +% from AlfaAesar, accessed on August 5, 2018 ( PDF )(JavaScript required) .
- ↑ Thomas' Chemistry: Synthesis of Anthranilamide , accessed August 5, 2018.
- ↑ Data sheet Anthranilamide, matrix substance for MALDI-MS, ≥99.0% (HPLC) from Sigma-Aldrich , accessed on August 5, 2018 ( PDF ).
- ↑ DLG: Packaging material made of polyethylene terephthalate (PET) , accessed on August 6, 2018.