| 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 |
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| 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Chemical Properties |
| Melting point | 258-261 °C(lit.) |
| Boiling point | 114℃ |
| density | 1.2945 (rough estimate) |
| refractive index | 1.8300 (estimate) |
| storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C |
| solubility | Chloroform (Slightly), DMSO (Slightly) |
| pka | 3.65±0.10(Predicted) |
| form | Solid |
| color | White to Light Yellow |
| CAS DataBase Reference | 1668-54-8(CAS DataBase Reference) |
| EPA Substance Registry System | 1,3,5-Triazin-2-amine, 4-methoxy-6-methyl- (1668-54-8) |
| Safety Information |
| 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 |
| Provider | Language |
|---|---|
| ACROS | English |
| SigmaAldrich | English |
| 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 |
