GB 28127-2011 English PDFUS$259.00 · In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. GB 28127-2011: [GB/T 28127-2011] Chlorsulfuron technical material Status: Valid
Basic dataStandard ID: GB 28127-2011 (GB28127-2011)Description (Translated English): [GB/T 28127-2011] Chlorsulfuron technical material Sector / Industry: National Standard Classification of Chinese Standard: G25 Classification of International Standard: 65.100.20 Word Count Estimation: 10,176 Date of Issue: 2011-12-30 Date of Implementation: 2012-04-15 Quoted Standard: GB/T 1600; GB/T 1601; GB/T 1604; GB/T 1605-2001; GB 3796; GB/T 19138 Adopted Standard: FAO specification 391/TC-2003, MOD Regulation (derived from): Announcement of Newly Approved National Standards No. 23 of 2011 Issuing agency(ies): General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China Summary: This Chinese standard specifies the original drug Chlorsulfuron requirements, test methods and marking, labeling, packaging, storage and acceptance period. This standard applies to chlorsulfuron and impurities generated in the production of chlorsulfuron original drug. GB 28127-2011: [GB/T 28127-2011] Chlorsulfuron technical material---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.Chlorsulfuron technical material ICS 65.100.20 G25 National Standards of People's Republic of China Chlorsulfuron TC Published 2011-12-30 2012-04-15 implementation Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China Standardization Administration of China issued ForewordThis standard in Chapter 3, Section 5 is mandatory, the rest are recommended. This standard was drafted in accordance with rules GB/T 1.1-2009 given. This draft standard method using the reformed modified using FAOspecification391/TC (2003) "chlorsulfuron TC" (Chlorsulfuron To technical differences and the reasons are as follows. --- This standard increased the water content, pH value range, mass fraction insoluble in acetone was controlled more comprehensive index item, character Combined domestic pesticide registration requirements, FAO specifications not control these three indicators. Please note that some of the content of this document may involve patents. The issuing authority of this document does not assume responsibility to identify these patents. The standard proposed by China Petroleum and Chemical Industry Association. This standard by the National Pesticide Standardization Technical Committee (SAC/TC133). This standard is drafted. Shenyang Chemical Research Institute Co., Ltd. Participated in the drafting of this standard. Hormone Research Institute Co., Ltd., Jiangsu Province, Shenyang harvest pesticides Limited. The main drafters. Jiang Minyi, Xing Jun, Fan Lei, Wang Yang. Chlorsulfuron TC1 ScopeThis standard specifies the requirements chlorsulfuron original drug, Test Method for marking, labeling, packaging, storage and acceptance period. This standard applies to impurities derived from the production of chlorsulfuron and the composition of the original drug chlorsulfuron. Note. Other names, structural formulas and physicochemical parameters of the basic chlorsulfuron see Appendix A.2 Normative referencesThe following documents for the application of this document is essential. For dated references, only applies to the version dated paper Pieces. For undated references, the latest edition (including any amendments) applies to this document. GB/T 1600 Pesticide Method Moisture Determination 1601 pH value pesticides GB/T GB/T 1604 pesticide regulations for acceptance of goods GB/T 1605-2001 sampling commercial pesticides GB 3796 pesticide packaging General GB/T 19138 Determination of acetone insoluble pesticide 3.1 Appearance White powdery solid. 3.2 Technical Specifications Chlorsulfuron TC should meet the requirements of Table 1. Table 1 TC control chlorsulfuron Item Index Item Index Chlorsulfuron mass fraction /% ≥ 95.0 Moisture content /% ≤ 0.5 The pH range of 3.0 to 6.0 Mass acetone insoluble fraction a /% ≤ 0.5 When a normal production, the acetone insoluble matter content measured at least once every three months. Test Method 4 4.1 Sampling Carried out in GB/T 1605-2001 of "original drug product sampling" approach. Determined by sampling a random number table method packages, the amount of the final sample Not less than 100g. 4.2 Identification Test Optionally one of the following methods. When not identified using a method, it should then be determined using another method. Infrared spectroscopy and chlorsulfuron --- Sample Sample infrared 4000cm-1 ~ 400cm-1 absorption spectrum should be no significant difference. Chlorsulfuron standard infrared spectra of Figure 1. FIG 1 chlorsulfuron standard IR spectrum HPLC --- This identification test can be carried out simultaneously with the determination of the mass fraction of chlorsulfuron. In the same chromatographic operating conditions Next, a peak in the sample solution and the retention time chlorsulfuron retention time of the standard solution chlorsulfuron peaks, the relative difference should 1.5% or less. 4.3 Determination of the mass fraction of chlorsulfuron 4.3.1 Method summary Sample solution was dissolved in methanol with aqueous ammonia, acetic acid in acetonitrile and water as mobile phase, using Nova-PakC18 filler to a stainless steel column And a UV detector (230nm), the sample chlorsulfuron and high performance liquid chromatography assay. 4.3.2 Reagents and solutions Methanol. HPLC grade; Acetonitrile. HPLC grade; Acetic acid; Water. The new secondary steam distilled water; Aqueous ammonia. w (NH3) = 26% ~ 30%; Ammonia solution. [Psi] (ammonia. water) = 1.300; Ammonia in methanol. [Psi] (ammonia solution. methanol) = 1.4; Chlorsulfuron Sample. chlorsulfuron known mass fraction, w≥98.0%. 4.3.3 Instruments HPLC. a variable wavelength UV detector; Chromatographic data processor or workstation; Color 150mm × 3.9mm (id) stainless steel column Nova-PakC18,5μm filler contents (or equivalent effect. Column Spectrum column); Filter. membrane pore size of about 0.45 m; Microsyringe. 50μL; Quantitative sampling tube. 5μL; Ultrasonic cleaning. 4.3.4 HPLC operating conditions Mobile phase. [Psi] (acetonitrile. water. glacial acetic acid) = 40.60.0.5; Flow rate. 1.0mL/min; Column temperature. room temperature (temperature change should be less than 2 deg.] C); Detection wavelength. 230nm; Injection Volume. 5μL; Retention time. chlorsulfuron about 4.3min. Are typical operating parameters of the above, according to the characteristics of different instruments, for a given operating parameters appropriately adjusted to obtain the best result. Typical chlorsulfuron HPLC TC shown in Figure 2. 1- chlorsulfuron. Figure 2 HPLC original drug chlorsulfuron 4.3.5 Determination Step 4.3.5.1 Preparation of standard solution Weigh 0.05g chlorsulfuron standard (accurate to 0.0002g), a 100mL volumetric flask, dilute to volume with methanol solution of ammonia, To dissolve the sample ultrasonic vibration 5min, cooled to room temperature, shaking. 4.3.5.2 Preparation of sample solution Weigh 0.05g of chlorine-containing specimens chlorsulfuron (accurate to 0.0002g), a 100mL volumetric flask, dilute to the mark with methanolic ammonia Degrees, to dissolve the sample ultrasonic vibration 5min, cooled to room temperature, shaking. 4.3.5.3 Determination Under the above operating conditions, after the instrument is stable, the number of consecutive doses of the standard solution is injected until the two needles chlorsulfuron relative change in peak area adjacent After less than 1.2%, measured according to the standard solution, sample solution, the sample solution, the order of standard solution. 4.3.6 computing The two needle and the sample solution was measured before and after the two doses of the standard sample solution chlorsulfuron peak area are averaged. Sample chlorsulfuron Mass fraction by formula (1). w1 = A2 · M1 · w A1 · m2 (1) Where. --- the mass fraction of the sample W1 chlorsulfuron, expressed in%; A2 --- sample solution, the average peak area chlorsulfuron; M1 --- chlorsulfuron standard mass in grams (G); W --- chlorsulfuron standard mass fraction in%; A1 --- the standard solution, the average peak area chlorsulfuron; --- M2 sample mass, in grams (g). 4.3.7 allows poor Results difference chlorsulfuron replicates should be less than twice the mass fraction of 1.2%, and the arithmetic mean value as a measurement result. 4.4 Determination of moisture content Carried out in GB/T 1600 in the Karl Fischer method. 4.5 pH value measured Carried out in GB/T 1601. 4.6 Determination of the mass fraction of acetone insoluble According to GB/T 19138 carried out. 4.7 product testing and acceptance It should conform to GB/T 1604 a predetermined limit value value comparison treatment using the rounding method. 5 marking, labeling, packaging, storage, security, acceptance period 5.1 marking, labeling, packaging Flag chlorsulfuron original drug, labeling and packaging should comply with the provisions of GB 3796. Drugs chlorsulfuron original clean plastic bag lined Bag or fiber drum lined with clean plastic bag, barrel net content is generally 25kg. The user may also request or order agreement Other forms of packaging, subject to the provisions of GB 3796. 5.2 Storage Chlorsulfuron original drug package airiness, dry place; storage and transportation, prevent moisture and sunlight, no food, seeds and feed Mix, to avoid contact with the skin, eyes, mouth and nose to prevent inhalation. 5.3 Security This product is a low toxicity of sulfonylurea herbicides. Are swallowed and inhaled toxic, it can penetrate through the skin. When using this product to avoid contact with the skin, After application with soap and rinse with water. Poisoning should immediately sent to hospital for symptomatic treatment. 5.4 Acceptance of Chlorsulfuron original drug acceptance period is one month. From the date of delivery, product quality inspection completed within one month, the indicators should be consistent standard requirement.Appendix A(Informative) Other names chlorsulfuron, structural formulas and physicochemical parameters of the basic This product is an active ingredient chloro other names, structural formulas and physicochemical parameters of the basic metsulfuron follows. ISO common name. Chlorsulfuron CAS Registry Number. 64902-72-3 CIPAC Numeric Code. 391 Chemical name. 1- (2-chlorophenyl) -3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea Structure. Empirical formula. C12H12ClN5O4S Molecular weight. 357.8 Biological activity. weeding Melting point. about 174 ℃ ~ 178 ℃ Vapor pressure (25 ℃). 3nPa Solubility (22 ℃, g/L). 57 acetone; dichloromethane 102; 14 methanol; toluene 3; hexane 0.01; water 0.1 ~ 0.125 (25 ℃, pH4.1), 0.3 (25 ℃, pH5) Stability. when dry, light stability; in the soil, due to hydrolysis and microbial degradation and damage; half-life in soil 150d ~ 160d. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB 28127-2011_English be delivered?Answer: Upon your order, we will start to translate GB 28127-2011_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of GB 28127-2011_English with my colleagues?Answer: Yes. 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