GB/T 19337-2017 in English
VALIDAbamectin emulsifiable concentrates
- Issued on:2017-11-01
- Implemented on:2018-05-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$156.00
本标准规定了阿维菌素乳油的要求、试验方法、验收、保证期以及标志、标签、包装、贮运。
本标准适用于由阿维菌素原药与乳化剂溶解在适宜溶剂中配制成的阿维菌素乳油。
Introduction
GB/T 19337—2017 Standard Overview
GB/T 19337—2017 Abamectin EC is an important standard in the pesticide field of the People's Republic of China, which is used to regulate the quality requirements, test methods and storage and transportation conditions of Abamectin EC. This standard replaces the old version of the standard GB/T 19337—2003. The main technical changes include the clear provisions of the mass fraction of Abamectin, the optimization of the ratio of B₁a to B₁b, and the addition of a new persistent foaming control item.
Comparison of standard frameworks
| Project dimensions | Old version of the standard (GB/T 19337—2003) | New version of the standard (GB/T 19337—2017) |
|---|---|---|
| Quality indicators | The specific value of the mass fraction of avermectin is not clear | The mass fraction of avermectin is stipulated as 1.8%, 3.2%, 5.0% and 10.0% |
| Ratio of B₁a to B₁b | Not less than 4.0 | Not less than 10.0 |
| Control Items | Persistent Foaming is Not Included | Added Persistent Foaming (≤60mL) |
Technical Background and Evolution Analysis
Avermectin is a pesticide widely used to kill insects and mites. Its emulsifiable concentrate form is highly favored due to its high solubility and stability. The technical upgrade of the new version of the standard reflects the industry's higher requirements for product quality and safety:
- Mass fraction: The technical indicators of products with different concentrations are clearly defined to ensure product consistency.
- Optimization of the ratio of B₁a to B₁b: Higher ratio requirements improve product quality and stability.
- Added Persistent Foaming Control: This reflects the focus on the performance of emulsifiable concentrate products to avoid excessive foam affecting the application effect.
Test methods and implementation suggestions
Optimized application of high performance liquid chromatography
The new standard recommends the use of high performance liquid chromatography (HPLC) for the quality analysis of avermectin. The specific operating conditions include:
- Mobile phase ratio: methanol: acetonitrile: water = 45:40:15.
- Detection wavelength: 245nm, suitable for ultraviolet detection of avermectin.
- Chromatographic column requirements: C₁₈ filler, inner diameter 4.6mm, length 250mm.
Through case analysis, it was found that this method has the characteristics of good separation effect, high sensitivity and good repeatability, and is particularly suitable for the quality control of avermectin emulsifiable concentrate.
Implementation Suggestions
To ensure the effective implementation of the standard, it is recommended that:
- Enterprises should be equipped with advanced analytical equipment and professional technical personnel.
- Strictly control the quality and proportion of raw materials during the production process.
- Regularly conduct low temperature stability, heat storage stability and emulsion stability tests to ensure the long-term consistency of product quality.

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