| Specification for Emamectin 70%TC | |
|---|---|
| ITEMS | STANDARDS |
| Appearance | White to beige powder |
| Content of a.i. | ≥70% |
| B1a/B1b | ≥ 20.0 |
| Water | ≤2.0% |
| pH | 4.0~8.0 |
| Acetone insolubles | ≤0.5% |
| Specification for Emamectin 2% EC | |
| ITEMS | STANDARDS |
| Appearance | Homogeneouslight yellowliquid |
| Content of a.i. | ≥2.0% |
| B1a/B1b | ≥ 20.0 |
| Water | ≤0.8% |
| pH | 4.0~7.5 |
| Emulsion stability (as 0.5% aqueous solution) | Qualified |
| Stability at 0℃ | The volume of solid and/or liquid which separates shall not be more than 0.3 ml. |
| Specification for Emamectin 5%WDG | |
| ITEMS | STANDARDS |
| Appearance | White to light beige, flowable granules |
| Content of a.i. | ≥5% |
| B1a/B1b | ≥ 20.0 |
| Wet sieve (through 75μm sieve) | ≥98% |
| Suspensibility | ≥80% |
| Disintegration time | ≤180s |
Packing: net 25kg in bag or drum or according to client’s requirement.
