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| 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Basic information |
Product Name: | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | Synonyms: | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine,97%;s-Triazine, 2-amino-4-methoxy-6-methyl-;2-AMINO-4-METHOXY-6-METHYL-S-TRIAZINE;2-AMINO-4-METHOXY-6-METHYL-1,3,5-TRIAZINE;2-AMINO-4-METHYL-6-METHOXY-1,3,5-TRIAZINE;TIMTEC-BB SBB004163;2-Amino-4-methoxy-6-;2- aMino-4-Methoxy -6-Methyl -1,3,5-three work | CAS: | 1668-54-8 | MF: | C5H8N4O | MW: | 140.14 | EINECS: | 216-790-7 | Product Categories: | Amines;Building Blocks;Heterocyclic Building Blocks;Triazines | Mol File: | 1668-54-8.mol | |
| 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Chemical Properties |
Hazard Codes | Xn | Risk Statements | 22-36/37/38 | Safety Statements | 26-36-37/39 | WGK Germany | 1 | RTECS | XY3193000 | HazardClass | IRRITANT | HS Code | 29336990 | Toxicity | LD50 oral in mouse: 1010mg/kg |
| 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Usage And Synthesis |
Chemical Properties | off-white to light yellow powder | Uses | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine may be used in the synthesis of thifensulfuron. | Definition | ChEBI: A monoamino-1,3,5-triazine that is 1,3,5-triazin-2-amine substituted by a methoxy group at position 4 and a methyl group at position 6. It is a metabolite of the herbicide thifensulfuron-methyl. | General Description | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine is formed during the photocatalytic decomposition of sulfonylurea (Sus) herbicide. It is also formed as a thermal decomposition product of chlorsulfuron (a sulfonylurea herbicide) and has been determined by GC using nitrogen-phosphorus detection (NPD). |
| 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Preparation Products And Raw materials |
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