Some standard content:
Chemical Industry Standard of the People's Republic of China
HG3291~3297—2001
(2001)
Published on January 24, 2002
Implemented on July 1, 2002
Published by the State Economic and Trade Commission
Registration No.: 10082—2002
HG3295-2001
Chapter 3 and Chapter 5 of this standard are mandatory, and the following are recommended. This standard is a derivative of Chemical Industry Standard HC23—1989—Oxazolone Powder 3. The main technical difference between this standard and HG25—89 is: the pH value index 16.0~9.0 is changed to 6.0~10.5. The cumulative floating rate indication shall be uniformly stipulated as greater than or equal to ten times, and the quantity control index of the factory shall be stipulated as less than or equal to (1). This standard is difficult to implement. It is the same as the H3294-1989 standard issued by the State Administration of Petroleum and Chemical Industry. The National Pesticide Standardization Technical Committee is responsible for the technical coordination of the National Pesticide Standardization Committee. The drafting unit of this standard is: Shenyang Chemical Industry Research Institute. The co-drafting units of this standard are: Sichuan Gao Chemical Research and Design Institute, Jiangsu Shihu Pesticide Adjuvant, Jiangsu Zhangjiagang Second Pesticide Co., Ltd. The main drafters of this standard are: Gong Yifan, Nai Ling Zhou Sihua, Bu Xing, Xu Xiangsheng, Mao Hong. This standard was first issued in 1985 as an industry standard. It was converted into a mandatory chemical industry standard in 1999 and was newly numbered as HC 320=-1989.
This standard is entrusted to the Secretariat of the National Pesticide Standardization Technical Committee for interpretation. 37
Chemical Industry Standard of the People's Republic of China
Triadimefon Wettabke powders
Other names, structural formulas and basic chemical information of triadimefon are as follows: IS common name, Triadimefon
CEPAC digital code: 552
Chemical name: 1-(-phenyl)-7.:(1H:2,2-oxazol-1-yl)-3,3-dimethylbutyl 2-one Structural formula:
Experimental CCIN
Data of molecular weight: 253.75 (according to the 1997 Internet atomic weight) Bioactivity: Soft
Melting point 32. 3
Vapor (20.1ml
I[G 3295—2D1
Beijing 3263-1969
Brightness (g/20), 0.0% in water, 1C--20 in n-calcined methane greater than 255, 100~2F in cyclohexane 600~12:.1.40 in toluene)-60
This standard defines the requirements, test methods and marking, labeling, packaging and transportation of triazole wettable powders. This standard is applicable to triazole wettable powders made from azole precursors that meet the standard and suitable homogenizing agents. 2
Inhalation standard
The provisions of the following standards are included in the provisions of the standard through the use of the standard. At the time of publication of this standard, the versions shown are valid. All standards will be revised. All parties using this standard should discuss and use the latest version of the following standard to measure the viscosity of the product. GB/T601-1989 Preparation of standard for titration analysis of chemical reagents (volume fraction) (3/1601-1993 Method for determination of pH value of pesticides GR/T1e4995 Acceptance rules for agricultural products
GT/T1605-379 (1989) Method for sampling of commercial pesticides 379% 1999 General rules for pesticide packaging
GB/T515.-1986 Method for determination of the properties of pesticides H/1148251993 Method for determination of floating rate of wettable powders of pesticides GB/6:50-1495 Method for determination of fineness of wettable powders of pesticides Method for formulation Approved by the Economic and Trade Commission on January 24, 2002 Implementation on July 1, 2002
3 Yunqiu
HG3295-2001
3.1 External, consider the looseness of the uniform, no lumps. 3.2 = The reverse process can be made to meet the requirements of Table 2, Table 1 Triazole wettability agent preparation items Daily index Month
Lan ton feather combination, 5
For the rate of compliance and,
Very economical, "
The time to
Fineness of the electric 4 sieve
Chicken furnace method rotten
0. 0.~ 13. 5
: During normal production, the qualitative test shall be conducted at least once every three months. The test method shall be in accordance with the sampling method of powder mixable powder in G3/116051979:1585. The sampling items shall be determined by the random number table method, and the final sampling shall not be less than 20 products. 4. 2. Gas chromatography: This identification test is carried out simultaneously with the determination of the content of the product. Under the same chromatographic operating conditions, the relative value between the retention time of a certain chromatographic peak of the test sample and the retention time of the triacetin peak in the standard sample solution should be within 1.5. Under the conditions of alternating chromatographic operation, the relative difference between the retention time of the chromatographic peak of the sample solution and the retention time of the triacetin in the standard solution should be within 1.0. 4.3 Determination of triacetin content 4.3.1 The sample is decomposed with monochloroethane to obtain di-n-butyl ester. Or ortho-butyl ester ortho-butyl ester as internal standard, use 30V-1?/l-1rlAWM as filler stainless steel and gold wax ionization detector, and perform gas separation and analysis on the type of test.
4.3.2 Test and liquid
Triazine.
Two-stage standard sample, containing greater than or equal to 9S.0%. Standard substance: "butyl ester or ortho-butyl ester, should not have ten impurities that interfere with the analysis: OV17.
Find a car, ChrusrbGAWDMcs (130-~250): Internal filling: Weigh: 2. 100 g of butyl carboxylate or 7.50 g of dibutyl succinate dicarboxylate can be placed in a 1000 mL volumetric flask and the H 2 O 3 solution is decomposed into a desired product by shaking. 4.3.3 Instrument || tt || Phase chromatograph with a hydrogen trap ionization detector. 10
Color source data processor,
Color enhancement column: 1m×3mi.d>Stainless steel pull.
HG3295—2001
Substituent: 1 on ChromoaorbGAwDMcs(1s~250pnt. Fixed wave: (fixed liquid-carrier) 310n (mass ratio) 4.3.4 Preparation of chromatographic solution
4.3.4.1 Preparation of fixed solution
It is difficult to take 0.0V-?Fixed wave in a 250mL beaker, add appropriate amount (slightly larger than the carrier volume) of ketone. Use a stirring finger to dissolve. 17 is completely dissolved, 4.3.4.2 Filling the environment with the required amount of filler
Connect the small end to the outlet of the color column that has been dried, and fill the prepared filler into the column. Gently place the column wall until the filler is 1.5m away from the outlet. Move the bucket to the entrance of the color column, plug a small piece of alkylated glass at the outlet, connect it to the vacuum object through a rubber hose, start the vacuum pump, continue to add filler regularly, and close the channel to make the environment filled. Filling is also completed, at the inlet end, also Small balls of glass are evenly packed, and when pressed, they are allowed to move. 4.3.4.3 Aging of the color column
Connect the color column outlet to the vaporization chamber and do not connect it to the detector. Pass the carrier gas at a flow rate of 10mL/min (below), and fill it with this temperature for at least 24h. 4.3.5 Gas phase spectrometry operation temperature (℃: 2U1, vaporization chamber 230, detector chamber 250: gas volume (ml/mia): N30, hydrogen 3C air 303 maintenance time (): 12, the second product is about 163, the second steam is about 10 It is typical that the given operating parameters can be adjusted appropriately according to the characteristics of different instruments in order to achieve the best effect. The typical gas and color of triazole wettable powder are shown in Figure 1. 1 Potentiometer; 2 Dimethicone 13 Dimethicone 11-1 ...12 (accurate 0.100) 2g, put into 25mL volume, use the same tube as 4.3. 1 to obtain the internal standard. 4.3.6. 3 Measure. Under the above chromatographic conditions, wait for the instrument to stabilize and inject several sample solutions. Calculate the relative response of each solution until the response of the two solutions changes by less than 1%. According to the actual sample solution, the sample solution and the standard sample solution, inject and analyze. 4.3.7 Sieve. The two solution solutions are measured and the ratio of the peak of the two standard solutions to the internal standard is calculated by half-averaging: The mass fraction X of the peak in the sample is calculated by formula 1): X,
Average value of the peak area ratio of the three electrochemical standard substances in the standard sample solution: The peak area ratio of the triadimefon internal standard substance in the sample solution is almost constant!
Test sample quantity:
Mass fraction of triadimefon in the sample, %.
4.3.8 The difference between the results of two parallel determinations shall not be greater than! 1. The arithmetic mean is taken as the test result: 4.4 Determination of the total content of the sample 4.4.1 Method The sample is dissolved in acetonitrile, acetonitrile water is used as the driving liquid, and a phase chromatograph with a particle size of 1-10 μm as the filler and a UV detector (E) is used to separate and determine the hydrochloric acid in the sample according to the standard method. 4.4.2 Reagents and solutions: Color clear: freshly distilled water, mobile phase: (CHCN: H2SO4) 49:1, degassed in a 1.1 μm pore membrane filter in a sonic bath with a 10-in. The total content of the sample is 9.0. 4.4. 3. High efficiency chromatography: with fixed wave UV detection instrument Note: 24ii.d.1 stainless steel. 1.r filler, particle size um, filter membrane pore size 0.45 4.4.4 High efficiency droplet chromatography operating parameters CIC: H () = 5 1.0 m short mixing chamber. Test liquid: 276 LE input volume, 10 L retention time: extractant mim HG3295-2001 above Parameters are not typical. Different instruments require different settings. Please make appropriate adjustments to the color and environment. Figure 2.1 shows the subtraction chromatogram of phenol in the wettable powder of the present invention. 4.4.5 Determination of the chromatographic conditions of phenol in the natural agent. 4.4.5.1 Preparation of standard sample solution. Take 3.0002 g of standard sample C.05 fine powder and place it in a volumetric flask. Dissolve it in ethanol. Pipette 101 ml of the concentrated sample by pipetting. Set aside. Add another 5 ml of the sample to a volumetric flask and dilute with ethanol until effective. .4.5.2 Preparation of sample solution
Take a sample containing about 2g of chloramine (accuracy 3.3002g), place it in a 100mL volumetric flask, and add 50ml accurately. Solution test: Oscillate the volumetric volume in an ultrasonic oscillation for 1(milliseconds) and wait until it reaches room temperature. Pass it through a 0.45m filter membrane. 4.4.5.3 Determine
Under the above conditions, the instrument is stable, and the standard wave is measured. When the net surface area of the two needles is less than 1:3, analyze the sample solution, sample solution, and mixed solution in this order according to the standard sample. d.4.6 Calculate
The measured The two sample data and the test sample's filter product of nitrogen non-phenol are averaged respectively, and the mass fraction x(w) of the test gas in the test group is calculated according to formula (2): 1AmP
Standard limit area
Average ammonia resistant area liquid in the sample, standard mass, g;
Test mass accumulation B:
IG3295—2001
The amount of sensitive extract in the standard sample is determined according to GB/T1601.
4.6 Determination of sensitive buoyancy
According to H/T1825. The sample is weighed to contain 0.158 of triazole (accurate to 0.1W2) in 25 ml of precipitate. Add 1 ml of internal standard in the same way as in 4.3.6. After full collection and centrifugation, take the organic phase and determine the mass of triazole in the remaining and precipitate according to 2.3. The buoyancy rate of triazole in the sample is calculated according to formula (3): x, m-1×11:.1
Prepare the mass of triazole in the test mold with low buoyancy. R! The mass of triazole in the floating and precipitated products is converted into the conversion coefficient of 25 ml.
111:7-
4.7 Determination of wetting time
According to GH/1 545.
4. Determination of fineness
According to the sieve inversion in 63T16155-1995. 4.9 Thermal migration qualitative
4.9.1 Method summary
The product is aged rapidly by pressurized heat test frequency, and the change of product performance is observed. 4.9.2 Apparatus
External: 230ml., internal diameter 0~5.5cm. Response: The maximum response is to produce an average service life of 2.15: 4.9.3 Tester
Put 20 test pieces into a beaker without any pressure, so that they are laid into a smooth and uniform layer of equal thickness. Press the disc on the sample, put it in a drying oven at (34-2) °C, store for 14 days, take out the beaker, take out the disc, put it into the drying oven, and cool the sample in the room for 10 minutes. The effective ingredient content and suspension rate should be determined within 215 °C. The effective ingredient content should not be less than 9% of the content obtained by heat expansion, and the basic rate should meet the standard requirements.
4.10 Product verification and acceptance
The heat and cold release of the product shall comply with the relevant provisions of CB/T1604. The rounded value shall be used for the treatment of the limit dispersion value: 5 Marking, labeling, packaging, storage and transportation
5.1 The labeling and packaging of the azole powder shall comply with the provisions of GB3796. 5.2 This product is packed with materials, and the net content of each pack is 200%. Another packing is a whole box, and the net content of each box is 2kg. 5.3 According to the user's requirements or the order agreement, other forms of packaging can be used, but it must comply with the provisions of GB37. 5.4 The packaging should be stored in a ventilated and dry warehouse. 5.5 During storage and transportation, the product should not be mixed with food, seeds, and feed, and should not be mixed with chlorinated peptides. Please avoid contact with the product. 5.6 In the instructions or packaging containers, the corresponding lifespan should be marked. It should also be stated that triadimefon is a low-toxic bacteriostatic agent. It is toxic if swallowed or inhaled. It can also enter through the skin. Wear protective gloves when using this product. When applying the medicine, it should be carried out in the direction of wind to prevent oral inhalation. After the skin or body exposed to the media is exposed to this product, it should be washed with soap and water. If chlorine is found in the accident, please consult a doctor. 5.7 Under the specified adverse conditions, the warranty period of Triazolam WP is: years from the production date.)49: :1, the membrane filter with a pore size of 1.1 μm was degassed in a sonic bath with a 10 -in. content of the whole book was pre-standardized, and the content of the mixture was equal to 9.0. 4. 4. 3 Only the group
high efficiency chromatography: the right can be fixed wave medical ultraviolet detection drama color language note: 24ii.d.1 stainless steel raw. Inside 1.r filler, particle size um is exceeded by the material slot,
can pass through the sincere energy: the filter membrane pore bell is 0.45
4.4.4 high efficiency droplet chromatography operating parts
CIC: H()=:5
said delivery: 1.0m
toe short: chamber mixing.
Test solution: 276LE
Inlet volume, 10L
Retention time: For extractant, please refer to HG3295—2001
The above parameters are not typical. Different instrumentation points should be used. Please make appropriate adjustments to the color and the given environment to achieve the best results. Figure 2.1 shows the subtraction chromatogram of phenol in the wettable powder of trifluoroacetic acid. 4.4.5 Determination steps: 4.4.5.1 Preparation of standard sample solution. Take the standard sample C.05 4.4.5.2 Preparation of sample solution
Take a sample containing about 2g of 1-azole (precision 3.3002g), put it in a 100mL volumetric flask, and add 50ml of ethanol accurately. Dissolve the sample in an ultrasonic oscillation for 1(milliseconds) and wait until it reaches room temperature. Pass it through a 0.45m filter membrane. 4.4.5.3
Under the above conditions, the color is stable, and the dye is measured by the standard wave, until When the net surface area of the two needles is less than .3, the sample solution, sample solution and stirred solution are analyzed in the order of standard sample. d.4.6 Calculation
The measured sample data of the two needles and the residual product of the standard sample are averaged respectively, and the mass fraction x(w) of the sample is calculated according to formula (2): 1AmP
Standard limit
Average surface area of the sample
Standard mass fraction, g;
Test mass fraction B:
IG3295-2001
The mass fraction of the extract in the standard sample, g, 4.5TT determination is carried out according to GB/T1601. 4.6 Determination of buoyancy rate is carried out according to H/T1825. The sample is weighed to contain 0.158 of triazole (accurate to 0.1W2), and 1\mL of internal standard is added to 25ml of the sample by the same method as in 4.3.6. After full collection and centrifugal separation, the organic phase is taken according to 2.3 to determine the mass of triazole in the residual and precipitate. The buoyancy rate of triazole in the sample is calculated according to formula (3): x, m-1×11:.1
Prepare the mass of triazole in the low buoyancy test mold R! The mass of triazole in the floating and precipitated products is i,
111:7-
Conversion coefficient.
4.7 Determination of wetting time
According to GH/1 545.
4. Determination of fineness
According to the sieve inversion in 63T16155-1995; 4.9 Thermal fertilizer migration qualitative
4.9.1 Method summary
The product is aged rapidly by pressurized heat test frequency, and the change of product performance is observed. 4.9.2 Apparatus
External: 230ml., internal diameter 0~5.5cm. Response: The maximum response is to produce an average service life of 2.15: 4.9.3 Tester
Put 20 test pieces into a beaker without any pressure, so that they are spread into a smooth and uniform layer of equal thickness. Press the disc on the sample, put it in a drying oven at (34-2) °C, store for 14 days, take out the beaker, take out the disc, put it into the drying oven, and cool the sample in the room for 10 minutes. The effective ingredient content and suspension rate should be determined within 215 °C. The effective ingredient content should not be less than 9% of the content obtained by heat expansion, and the basic rate should meet the standard requirements.
4.10 Product verification and acceptance
The heat and cold release of the product shall comply with the relevant provisions of CB/T1604. The rounded value shall be used for the treatment of the limit dispersion value: 5 Marking, labeling, packaging, storage and transportation
5.1 The labeling and packaging of the azole powder shall comply with the provisions of GB3796. 5.2 This product is packed with materials, and the net content of each pack is 200%. Another packing is a whole box, and the net content of each box is 2kg. 5.3 According to the user's requirements or the order agreement, other forms of packaging can be used, but it must comply with the provisions of GB37. 5.4 The packaging should be stored in a ventilated and dry warehouse. 5.5 During storage and transportation, the product should not be mixed with food, seeds, and feed, and should not be mixed with chlorinated peptides. Please avoid contact with the product. 5.6 In the instructions or packaging containers, the corresponding lifespan should be marked. It should also be stated that triadimefon is a low-toxic bacteriostatic agent. It is toxic if swallowed or inhaled. It can also enter through the skin. Wear protective gloves when using this product. When applying the medicine, it should be carried out in the direction of wind to prevent oral inhalation. After the skin or body exposed to the media is exposed to this product, it should be washed with soap and water. If chlorine is found in the accident, please consult a doctor. 5.7 Under the specified adverse conditions, the warranty period of Triazolam WP is: years from the production date.)49: :1, the membrane filter with a pore size of 1.1 μm was degassed in a sonic bath with a 10 -in. content of the whole book was pre-standardized, and the content of the substance was equal to 9.0. 4. 4. 3 Only the group
high efficiency chromatography: with fixed wave medical ultraviolet detection play color language note: 24ii.d.1 stainless steel. Inside the 1.r filler, the particle size um is exceeded,
through the sincere energy: the filter membrane pore size is 0.45
4.4.4 high efficiency droplet chromatography operating equipment
CIC: H()=:5
said delivery: 1.0m
toe short: chamber mixing.
Test solution: 276LE
Inlet volume, 10L
Retention time: For extractant, please refer to HG3295—2001
The above parameters are not typical. Different instrumentation points should be used. Please make appropriate adjustments to the color and the given environment to achieve the best results. Figure 2.1 shows the subtraction chromatogram of phenol in the wettable powder of trifluoroacetic acid. 4.4.5 Determination steps: 4.4.5.1 Preparation of standard sample solution. Take the standard sample C.05 4.4.5.2 Preparation of sample solution
Take a sample containing about 2g of 1-azole (precision 3.3002g), put it in a 100mL volumetric flask, and add 50ml of ethanol accurately. Dissolve the sample in an ultrasonic oscillation for 1(milliseconds) and wait until it reaches room temperature. Pass it through a 0.45m filter membrane. 4.4.5.3
Under the above conditions, the color is stable, and the dye is measured by the standard wave, until When the net surface area of the two needles is less than .3, the sample solution, sample solution and stirred solution are analyzed in the order of standard sample. d.4.6 Calculation
The measured sample data of the two needles and the residual product of the standard sample are averaged respectively, and the mass fraction x(w) of the sample is calculated according to formula (2): 1AmP
Standard limit
Average surface area of the sample
Standard mass fraction, g;
Test mass fraction B:
IG3295-2001
The mass fraction of the extract in the standard sample, g, 4.5TT determination is carried out according to GB/T1601. 4.6 Determination of buoyancy rate is carried out according to H/T1825. The sample is weighed to contain 0.158 of triazole (accurate to 0.1W2), and 1\mL of internal standard is added to 25ml of the sample by the same method as in 4.3.6. After full collection and centrifugal separation, the organic phase is taken according to 2.3 to determine the mass of triazole in the residual and precipitate. The buoyancy rate of triazole in the sample is calculated according to formula (3): x, m-1×11:.1
Prepare the mass of triazole in the low buoyancy test mold R! The mass of triazole in the floating and precipitated products is i,
111:7-
Conversion coefficient.
4.7 Determination of wetting time
According to GH/1 545.
4. Determination of fineness
According to the sieve inversion in 63T16155-1995; 4.9 Thermal fertilizer migration qualitative
4.9.1 Method summary
The product is aged rapidly by pressurized heat test frequency, and the change of product performance is observed. 4.9.2 Apparatus
External: 230ml., internal diameter 0~5.5cm. Response: The maximum response is to produce an average service life of 2.15: 4.9.3 Tester
Put 20 test pieces into a beaker without any pressure, so that they are spread into a smooth and uniform layer of equal thickness. Press the disc on the sample, put it in a drying oven at (34-2) °C, store for 14 days, take out the beaker, take out the disc, put it into the drying oven, and cool the sample in the room for 10 minutes. The effective ingredient content and suspension rate should be determined within 215 °C. The effective ingredient content should not be less than 9% of the content obtained by heat expansion, and the basic rate should meet the standard requirements.
4.10 Product verification and acceptance
The heat and cold release of the product shall comply with the relevant provisions of CB/T1604. The rounded value shall be used for the treatment of the limit dispersion value: 5 Marking, labeling, packaging, storage and transportation
5.1 The labeling and packaging of the azole powder shall comply with the provisions of GB3796. 5.2 This product is packed with materials, and the net content of each pack is 200%. Another packing is a whole box, and the net content of each box is 2kg. 5.3 According to the user's requirements or the order agreement, other forms of packaging can be used, but it must comply with the provisions of GB37. 5.4 The packaging should be stored in a ventilated and dry warehouse. 5.5 During storage and transportation, the product should not be mixed with food, seeds, and feed, and should not be mixed with chlorinated peptides. Please avoid contact with the product. 5.6 In the instructions or packaging containers, the corresponding lifespan should be marked. It should also be stated that triadimefon is a low-toxic bacteriostatic agent. It is toxic if swallowed or inhaled. It can also enter through the skin. Wear protective gloves when using this product. When applying the medicine, it should be carried out in the direction of wind to prevent oral inhalation. After the skin or body exposed to the media is exposed to this product, it should be washed with soap and water. If chlorine is found in the accident, please consult a doctor. 5.7 Under the specified adverse conditions, the warranty period of Triazolam WP is: years from the production date.The mass of oxadiazoles for floating and sinking is calculated by 111:7- ... 4.9.3 Tester
Put 20 test pieces into a beaker without any pressure to form a smooth and uniform layer of equal thickness. Press the disc on the sample and place the beaker in an oven at (34-2) °C for 14 days. Take out the beaker, take out the disc, put it in a dryer, and cool the sample in a room for 215 days to complete the determination of the effective ingredient content and suspension rate. The content of the effective ingredient determined shall not be less than 9% of the content obtained by heat expansion, and the average rate shall meet the standard requirements.
4.10 Product verification and acceptance
The heat and cold release of the product shall comply with the relevant provisions of CB/T1604. The rounded value shall be used for the treatment of the limit dispersion value. 5 Marking, labeling, packaging, storage and transportation
5.1 The labeling and packaging of the azole powder shall comply with the provisions of GB3796. 5.2 This product is packed with materials, and the net content of each pack is 200%. Another packing is a whole box, and the net content of each box is 2kg. 5.3 According to the user's requirements or the order agreement, other forms of packaging can be used, but it must comply with the provisions of GB37. 5.4 The packaging should be stored in a ventilated and dry warehouse. 5.5 During storage and transportation, the product should not be mixed with food, seeds, and feed, and should not be mixed with chlorinated peptides. Please avoid contact with the product. 5.6 In the instructions or packaging containers, the corresponding lifespan should be marked. It should also be stated that triadimefon is a low-toxic bacteriostatic agent. It is toxic if swallowed or inhaled. It can also enter through the skin. Wear protective gloves when using this product. When applying the medicine, it should be carried out in the direction of wind to prevent oral inhalation. After the skin or body exposed to the media is exposed to this product, it should be washed with soap and water. If chlorine is found in the accident, please consult a doctor. 5.7 Under the specified adverse conditions, the warranty period of Triazolam WP is: years from the production date.The mass of oxadiazoles for floating and sinking is calculated by 111:7- ... 4.9.3 Tester Www.bzxZ.net
Put 20 test pieces into a beaker without any pressure to form a smooth and uniform layer of equal thickness. Press the disc on the sample and place the beaker in an oven at (34-2) °C for 14 days. Take out the beaker, take out the disc, put it into a dryer, and cool the sample in a room for 215 days to complete the determination of the effective ingredient content and suspension rate. The content of the effective ingredient determined shall not be less than 9% of the content obtained by heat expansion, and the average rate shall meet the standard requirements.
4.10 Product verification and acceptance
The heat and cold release of the product shall comply with the relevant provisions of CB/T1604. The rounded value shall be used for the treatment of the limit dispersion value. 5 Marking, labeling, packaging, storage and transportation
5.1-The labeling and packaging of the azole powder shall comply with the provisions of GB3796. 5.2 This product is packed with materials, and the net content of each pack is 200%. Another packing is a whole box, and the net content of each box is 2kg. 5.3 According to the user's requirements or the order agreement, other forms of packaging can be used, but it must comply with the provisions of GB37. 5.4 The packaging should be stored in a ventilated and dry warehouse. 5.5 During storage and transportation, the product should not be mixed with food, seeds, and feed, and should not be mixed with chlorinated peptides. Please avoid contact with the product. 5.6 In the instructions or packaging containers, the corresponding lifespan should be marked. It should also be stated that triadimefon is a low-toxic bacteriostatic agent. It is toxic if swallowed or inhaled. It can also enter through the skin. Wear protective gloves when using this product. When applying the medicine, it should be carried out in the direction of wind to prevent oral inhalation. After the skin or body exposed to the media is exposed to this product, it should be washed with soap and water. If chlorine is found in the accident, please consult a doctor. 5.7 Under the specified adverse conditions, the warranty period of Triazolam WP is: years from the production date.
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