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| | Irgarol Basic information |
| Product Name: | Irgarol | | Synonyms: | N'-tert-Butyl-N-cyclopropyl-6-(Methylthio)-1,3,5-t;Cybutrin;Irgaguard A 2000;Irgaguard D 1071;Microban Additive IA 1;Nuocide 1051;1,3,5-Triazine-2,4-diaMine,N2-cyclopropyl-N4-(1,1-diMethylethyl)-6-(Methylthio)-;2-(tert-Butylamino)-4-(cyclopropylamino)-6-(methylthio)-1,3,5-triazine | | CAS: | 28159-98-0 | | MF: | C11H19N5S | | MW: | 253.37 | | EINECS: | 248-872-3 | | Product Categories: | paint;Heterocycles | | Mol File: | 28159-98-0.mol |  |
| | Irgarol Chemical Properties |
| Melting point | 128-1330C | | Boiling point | 428.0±28.0 °C(Predicted) | | density | 1.20±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | Water Solubility | Insoluble in water | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | pka | 4.13±0.10(Predicted) | | form | neat | | color | White to Almost white | | BRN | 792218 | | EPA Substance Registry System | Cybutryne (28159-98-0) |
| Hazard Codes | Xi;N,N,Xi | | Risk Statements | 43-50/53 | | Safety Statements | 36/37-60-61 | | RIDADR | UN 3077 | | WGK Germany | 2 | | RTECS | XY5850675 | | HazardClass | 9 | | PackingGroup | III | | HS Code | 29336990 | | Hazardous Substances Data | 28159-98-0(Hazardous Substances Data) | | Toxicity | LC50 (96 hr in salt water) in mysid shrimp, inland silverside, sheepshead minnow (ng/l): 400000, 1580000, 3500000; LC50 (96 hr in fresh water) in rainbow trout, bluegill sunfish (ng/l): 790000, 2600000 (Hall) |
| | Irgarol Usage And Synthesis |
| Chemical Properties | White Solid | | Uses | Booster algicide in antifouling paint. | | Uses | Photosystem-II (PSII) herbicide; inhibits photosynthetic electron transport in chloroplasts | | Uses | Irgarol is a highly specific and effective inhibitor of photosynthesis. This makes it ideal, combined with its very low water solubility, for use in long-life antifouling coatings for marine applicati
ons to prevent the growth of algae. | | Definition | ChEBI: A diamino-1,3,5-triazine that is 1,3,5-triazine-2,4-diamine carrying a N-tert-butyl, N'-cyclopropyl and a methylsulfanyl group at position 6. | | Metabolic pathway | Metabolism of irgarol 1051 by the fungus
Phanerochaete chrysosporium proceeds mainly via
partial N-dealkylation at the cyclopropylamino group,
resulting in a tentatively identified 2-methylthio-4-tert-
butylamino-6-amino-1,3,5-triazine. |
| | Irgarol Preparation Products And Raw materials |
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