- SECBUMETON
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2026-07-08
- CAS:26259-45-0
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 10000kgS
- SECBUMETON
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- $1.00
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2020-01-01
- CAS:26259-45-0
- Min. Order: 1KG
- Purity: 95-99%
- Supply Ability: 1ton
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| | SECBUMETON Basic information |
| | SECBUMETON Chemical Properties |
| Melting point | 87℃ | | Boiling point | 366.8°C (rough estimate) | | density | 1.1038 (rough estimate) | | refractive index | 1.7610 (estimate) | | storage temp. | 0-6°C | | form | Crystalline | | pka | 4.39±0.10(Predicted) | | Water Solubility | 619.6mg/L(20 ºC) | | BRN | 8981797 | | Henry's Law Constant | 2.8×103 mol/(m3Pa) at 25℃, Mackay et al. (2006) | | Major Application | agriculture
environmental | | InChI | 1S/C10H19N5O/c1-5-7(3)12-9-13-8(11-6-2)14-10(15-9)16-4/h7H,5-6H2,1-4H3,(H2,11,12,13,14,15) | | InChIKey | ZJMZZNVGNSWOOM-UHFFFAOYSA-N | | SMILES | CCNc1nc(NC(C)CC)nc(OC)n1 | | EPA Substance Registry System | Secbumeton (26259-45-0) |
| Hazard Codes | Xn,N | | Risk Statements | 22-36-50/53-21/22 | | Safety Statements | 60-61-36/37 | | RIDADR | UN3077 9/PG 3 | | WGK Germany | 3 | | RTECS | XY4980000 | | TSCA | TSCA listed | | HS Code | 29336990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Dermal
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2 | | Toxicity | LD50 oral in rat: 1gm/kg |
| | SECBUMETON Usage And Synthesis |
| Uses | Secbumeton may be used as an analytical reference standard for the quantification of the analyte in environmental samples, agricultural commodities and vegetable samples using different chromatography techniques. | | Definition | ChEBI: N-(butan-2-yl)-N'-ethyl-6-methoxy-1,3,5-triazine-2,4-diamine is a diamino-1,3,5-triazine that is N-(butan-2-yl)-N'-ethyl-1,3,5-triazine-2,4-diamine substituted by a methoxy group at position 6. It is a diamino-1,3,5-triazine and a methoxy-1,3,5-triazine. | | Production Methods | The industrial production of secbumeton involves the chemical modification of a s-triazine core, specifically 2-methoxy-4,6-dichloro-1,3,5-triazine. This intermediate undergoes nucleophilic substitution where the chlorine atoms are replaced by sec-butylamine and ethylamine, forming the active compound 2-sec-butylamino-4-ethylamino-6-methoxy-s-triazine. The process is typically carried out in organic solvents under controlled temperature and pH conditions to ensure selectivity and yield. After synthesis, the product is purified and formulated for agricultural use. | | General Description | Secbumeton belongs to the class of triazine herbicides, widely used in agriculture to obtain high yield productions. Its mode of action involves the inhibition of photosynthesis, thereby controlling thegrowthofgrassesand broadleafweeds. | | Mechanism of action | Inhibition of photosynthesis at photosystem II, absorbed by roots and leaves with limited translocation | | Pesticide Type | Herbicide |
| | SECBUMETON Preparation Products And Raw materials |
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