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[GB/T 28146-2011] 3% Gibberellic acid emulsifiable concentrates
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GB 28146-2011
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Basic data | Standard ID | GB 28146-2011 (GB28146-2011) | | Description (Translated English) | [GB/T 28146-2011] 3% Gibberellic acid emulsifiable concentrates | | Sector / Industry | National Standard | | Classification of Chinese Standard | G25 | | Classification of International Standard | 65.100.30 | | Word Count Estimation | 10,185 | | Date of Issue | 2011-12-30 | | Date of Implementation | 2012-04-15 | | Quoted Standard | GB/T 1600; GB/T 1601; GB/T 1603; GB/T 1604; GB/T 1605-2001; GB 4838; GB/T 6682-2008; GB/T 8170-2008; GB/T 19136; GB/T 19137 | | 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 3% gibberellic acid EC requirements, test methods and marking, labeling, packaging, storage and warranty. This standard applies to the original drug with gibberellic acid emulsifier dissolved in a suitable solvent mixture of the 3% gibberellic acid EC. |
GB 28146-2011: [GB/T 28146-2011] 3% Gibberellic acid emulsifiable concentrates---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.
3% Gibberellic acid emulsifiable concentrates
ICS 65.100.30
G25
National Standards of People's Republic of China
3% gibberellic acid cream
3% Gibberelicacidemulsifiableconcentrates
Issued on. 2011-12-30
2012-04-15 implementation
Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China
Standardization Administration of China released
Foreword
The standard Chapter 3, Chapter 5 is mandatory, the rest are recommended.
This standard was drafted in accordance with GB/T 1.1-2009 given rules.
Please note that some content of this document may involve patents, the issuing authority of this document does not assume responsibility for the identification of these patents.
The standard proposed by China Petroleum and Chemical Industry Association.
This standard by the National Standardization Technical Committee on Pesticides (SAC/TC133) centralized.
This standard was drafted. the Ministry of Agriculture, with the Swiss biotechnology Shanghai Co., Ltd., Zhejiang Qianjiang Biochemical Company Limited
Secretary, Jiangxi Ruifeng Sheng Chemical Co., Ltd.
The main drafters of this standard. Yu Rong, Wang Xiaoli, Li Youshun, Chentie Chun, Zhao Yonghui, Jiang Yifei, Chenming Lei, Zhu Jianxin, IWC benevolence.
3% gibberellic acid cream
1 Scope
This standard specifies the 3% gibberellic acid EC requirements, test methods and marking, labeling, packaging, storage and warranty.
This standard applies to the original drug gibberellic acid formulated with an emulsifier dissolved in a suitable solvent into a 3% gibberellic acid cream.
Note. Other name, structural formula and basic physicochemical parameters of gibberellic acid in Appendix A.
2 Normative references
The following documents for the application of this document is essential. For dated references, only the dated version suitable for use herein
Member. For undated references, the latest edition (including any amendments) applies to this document.
GB/T 1600 Determination of Water Pesticides
Determination of GB/T 1601 Pesticides pH value
GB/T 1603 Determination of emulsion stability of pesticide
GB/T 1604 Goods pesticide regulations for acceptance
GB/T 1605-2001 Sampling Method commercial pesticides
GB 4838 EC pesticide packaging
GB/T 6682-2008 analytical laboratory use specifications and test methods (ISO 3696. 1987, MOD)
GB/T 8170-2008 revised value represents about rules and limit values and judgment
GB/T 19136 Determination of Pesticide Thermal storage stability
GB/T 19137 Pesticide cryogenic stability Determination
3 Requirements
3.1 Composition and appearance
This product should meet the standards of the original drug made of gibberellic acid, a stable homogeneous oily liquid without visible suspended matter and sediment.
3.2 Technical Specifications
3% gibberellic acid EC shall comply with the requirements of Table 1.
Table 1 3% gibberellic acid EC Control Project Index
Item Index
Gibberellic acid mass fraction /% 3.0 0.3-0.3
Moisture content /% ≤ 5.0
a pH range of 2.5 to 4.5
Emulsion stability (diluted 200 times) Qualified
Low temperature stability a qualified
Thermal storage stability of a qualified
a low temperature stability test, thermal storage stability test in the normal production and testing at least once every three months.
Test Method 4
Safety Tips. Use of this standard shall have practical experience of laboratory personnel work. This standard does not point out all of the safety issues. Make
With those who have the responsibility to take appropriate safety and health practices and to ensure compliance with the relevant national regulations.
4.1 General provisions
This standard reagents and water in the absence of other requirements specified, refers to three analytical reagent and GB/T 6682-2008 specified in
water. Test results determined in accordance with GB/T 8170-2008 4.3.3 Rounding the value comparison method.
4.2 Sampling
According to GB/T 1605-2001 in "liquid formulations sampling" approach. Random sampling method is determined by the package, the final sample size should not be
Less than 200mL.
4.3 Identification Test
The identification test can be carried out simultaneously with the determination of the mass fraction of gibberellic acid. Under the same chromatographic operating conditions, the main sample solution chromatogram
Retention time and peak standard solution of gibberellic acid chromatographic peak retention time, the relative difference should be less than 1.5%.
4.4 Determination of the mass fraction of gibberellic acid
4.4.1 Method summary
Sample dissolved in mobile phase, methanol - phosphoric acid as the mobile phase, use as filler to C18 stainless steel column and UV detector, for
Gibberellic acid in the sample by reverse phase HPLC separation and determination of external standard.
4.4.2 Reagents and solutions
Phosphoric acid;
Methanol. HPLC grade;
Water. The new secondary steam distilled water;
Phosphoric acid. [Psi] (water. phosphoric acid) = 2000.1;
Gibberellic acid standard sample. a known mass fraction w≥98.0%.
4.4.3 Instruments
High performance liquid chromatography. a variable wavelength UV detector and quantitative injection valve;
Chromatographic data processor or chromatography workstation;
Column. 250mm × 4.6mm (id) stainless steel column, built ZORBAXEXTENDC18,5μm filler (or with the same
Other effects such as columns);
Micro injector. 100μL;
Filter. filter pore size of about 0.45μm;
Ultrasonic cleaner.
4.4.4 HPLC operating conditions
Mobile phase. [Psi] (methanol. aqueous phosphoric acid solution) = 35.65;
Flow rate. 1.0mL/min;
Column temperature. room temperature (temperature change should not exceed 2 ℃);
Detection wavelength. 210nm;
Injection volume. 10μL.
Retention time. gibberellic acid about 8.2min.
HPLC operating conditions described above, the Department of typical operating parameters, according to the characteristics of different instruments, given operating parameters to make appropriate adjustments to
To obtain the best results. A typical 3% gibberellic acid cream HPLC is shown in Figure 1.
1 --- gibberellic acid.
1 3% gibberellic acid by high performance liquid chromatogram EC
4.4.5 measuring step
4.4.5.1 preparation of standard solution
Weigh gibberellic acid standard about 0.05g (accurate to 0.0002g), placed in 100mL flask, add 35mL of methanol to dissolve, then
Phosphoric acid aqueous solution was diluted to the mark.
4.4.5.2 preparation of the sample solution
Weigh a sample containing about 0.05g of gibberellic acid (accurate to 0.0002g), placed in 100mL flask, add 35mL of methanol to dissolve,
Phosphoric acid aqueous solution and then diluted to the mark. Filtered through a 0.45μm pore size filters.
4.4.5.3 Determination
Under these operating conditions, after the instrument is stable, continuous injection of several doses of the standard solution until the two adjacent needles gibberellic acid peak area relative change
After less than 1.5%, according to the solution, sample solution, sample solution, standard order of standard solution was measured.
4.4.6 Calculation
The two needle sample solution and measured before and after the two doses of the standard sample solution of gibberellic acid peak area were averaged. Sample gibberellic acid
Mass fraction w1 (%) according to equation (1).
w1 = A2
· M1 · w
A1 · m2
(1)
Where.
A2 --- sample solution, gibberellic acid, the average peak area;
m1 --- gibberellic acid standard sample mass in grams (g);
w --- Sample mass fraction of gibberellic acid,%;
A1 --- standard solution, gibberellic acid, the average peak area;
m2 --- sample mass, in grams (g).
4.4.7 allowable difference
The difference between two parallel determination results shall not be greater than 0.2%, the arithmetic mean value as a measurement result.
4.5 Determination of Moisture
According to GB/T 1600 the "Karl Fischer method".
Determination of 4.6 pH value
According to GB/T 1601 carried out.
4.7 Emulsion stability test
According to GB/T 1603 test. No oil slick in the cylinder (cream), heavy oil and precipitated as qualified.
4.8 Low temperature stability test
According to GB/T 19137 in "homogeneous emulsion and liquid preparations", in the bottom of the centrifuge tube educt volume does not exceed 0.3mL qualified.
4.9 Thermal storage stability test
According to GB/T 19136 in "liquid formulation" to. After the thermal storage, gibberellic acid content shall not be less than 95% before the heat storage mass fraction; milk
Liquid stability should still meet the standards.
4.10 Product inspection and acceptance
Shall comply with GB/T 1604's.
5 marking, labeling, packaging, storage, security and guarantee period
5.1 mark, label
3% gibberellic acid EC marking, labeling and packaging should comply with the provisions of GB 4838.
5.2 Packaging
3% gibberellic acid application with the EC within the plug and cover brown glass bottle or PET bottle packaging, bottle net content of 100mL (g),
200mL (g), 500mL (g); overpack Plastic boxes or corrugated boxes, each box net content not exceeding 15kg. According to user requirements or set
Goods agreement, the use of other forms of packaging, it should comply with the provisions of GB 4838.
5.3 Storage
3% gibberellic acid cream package should be stored in ventilated, cool, dry coffers, fire, moisture, and can not be in the open air with toxic substances,
Flammable material and alkaline material stacked together. Not with food, seeds, feed mixed release.
Storage and transportation to prevent moisture and sun, and rain to avoid collision, away from fire.
5.4 Security
This product is a low toxicity plant growth regulator. The FDA should wear protective gloves, masks, wearing clean protective clothing. When you can not use with a base
Items mixed, not be mixed with ammonia, calcium polysulfide, soda ash and the like. Used with the distribution, once dubbed the aqueous solution can not go far. Shall immediately after use
Wash with water. In case of poisoning, should go to hospital for treatment.
5.5 Warranty Period
Under the specified conditions of storage, 3% of gibberellic acid to ensure EC, two years from date of manufacture.
Appendix A
(Informative)
Other names gibberellic acid, structural formula and basic physicochemical parameters
This product is an active ingredient gibberellic acid is another name, structural formula and basic physicochemical parameters are as follows.
ISO common name. Gibberelicacid
CIPAC Numeric Code. 307
CAS Registry Number. 77-06-5
Chemical name. (1α, 2β, 4aα, 4bβ, 10β) -2,4a, 7- trihydroxy-1-methyl-8-methyl-3-ene-1,10-gibberellic acid -1 , 4a-
Lactone
Structure.
Empirical formula. C19H22O6
Molecular Weight. 346.4
Biological activity. Plant Growth Regulator
Melting point. 223 ℃ ~ 225 ℃ (decomposition)
Solubility. water 5g/L (room temperature). Soluble in methanol, ethanol, acetone, alkaline aqueous solution, slightly soluble in diethyl ether and ethyl acetate, insoluble
Chloroform. Its potassium, sodium, ammonium salts soluble in water (potassium salt 50g/L)
Stability. At room temperature in a dry state is stable, slow degradation in aqueous or aqueous alcohol solution in, DT50 (20 ℃) about
14d (pH3 ~ 4), 14d (pH7), alkali metal will be converted into less biologically active compounds, the case of thermal decomposition.
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