1. Wheat disease prevention
(A) wheat smut. With carbendazim active ingredient 100 g, add water 4kg evenly sprayed 100k Kemerovo kind, then pile boring six hours after seeding. Also available in multi-drop active ingredient 156 g, 156 kg of water, stir, dip 36 to 100 kg of wheat seed. When, then remove and planting. Liquid can be used continuously.
(2) wheat scab. As early flowering wheat continuous rainy weather, with a 25% wettable powder 2 150 to 200 grams per 667 meters, 50 to 80 liters of water spray, every 5 to 7 days depending on weather conditions and progression of the disease, decided to spray a second drug or not, with the first dosage.
2. Anti-consistent rice disease
(1) rice blast. Each 667 m z with carbendazim 37.5 to 50 g active ingredient, as a constant dilution water or low-volume spray. Prevention leaf blast, spraying in the field found when the disease first drug center, then spray once every seven days. Prevention panicle blast in rice breach period and heading stage of the spray ~ times.
(2) rice sheath blight. Late tillering and booting once before each spraying. Each
667 m 2 with carbendazim active ingredient 37.5 to 50 grams of water spray. When spraying focus
Spray rice stem.
(3) Rice sclerotia. Round rice stalk jointing to heading spraying. 2 with the active ingredient per 667 meters carbendazim 37.5 to 50 g, 50 to 80 liters of water spray. Spraying every 5 to 7 days, a total of 2 to 3 times spraying.
3. Control of cotton disease control cotton blight, anthracnose, per 100 kg seeds with carbendazim active ingredient 500 g seed dressing. Soaking method may also be employed with active ingredient 250 g carbendazim, 250 kg of water, 100 kg of seed 24 hours immersion.
4. Prevention of Sclerotinia in canola flower flowering period and end the spray once. 2 with the active ingredient per 667 meters carbendazim 37.5 to 62.5 g, 50 to 80 liters of water spray.
5. Prevention peanut blight, stem rot, root rot by 50% carbendazim WP dressing. Dressing dose was 0.5% 81% seed weight, ie 100 kg seeds with 50% carbendazim WP 500 to 1000 grams. First peanut can also soak 24 hours or seeds moistened with water, then the above dosage dressing.
6. Prevention sweet black spot with 20,000 times the soaking liquid potato 10 minutes, or 30 mg / kg of liquid immersion seedlings base 3 to 5 minutes, the liquid can be used continuously for seven to 10 times.
7. Vegetable Diseases Prevention
(A) tomato early blight. Early onset of each ’667 m 2 with carbendazim active ingredient 31.3 ~ 37.5 g, 50 liters of water spray. Spray every 7 to 10 days time, continuous spraying three to five times.
(2) cucumber anthracnose. 25% carbendazim WP two thousand gram farmyard manure 2000 kg, with medicine soil cover.
8. Prevention and treatment of diseases of fruit trees
(1) pear scab. In budding pear with 25% carbendazim WP 250 times, spraying the first drug, after falling spray a second time. After spraying times decided according to the disease development. General spraying 3 to 4 times, each time interval of 7-10 days.
(2) peach scab. Before peaches bagging, wet with 25% carbendazim uh H agent 200 to 400 times spray, spray 7-10 off every time.
(3) apple leaf spot. In the beginning of the disease see below, using 25 cYo carbendazim W wettable powder spray 250 to 400 times. Spraying a second every 7 to 10 days.
(4) grape white rot, anthracnose disease, anthrax. After the grapes before leaf to fruit color, use 25% carbendazim WP 250 to 500 times the liquid spray, spray once every 10 to 15 days.
9. Prevention carbendazim dahlia flower rot, rose leaf spot, leaf spot Clivia, Begonia gray leaf spot, orchids anthracnose, leaf spot, powdery mildew and other flowers have some preventive effect floral diseases. Usage occurs early in the disease, the use of 25% Carbendazim 250 times spray. According to the progression of decisions spraying times. Spray every 7 to 10 days time.
Fipronil use
Fipronil broad spectrum insecticide with contact, stomach poisoning and moderate suction effect within. Both to control soil pests, but also prevention of ground pests. Both for leaf and soil treatment, but also for seed treatment. 25 ~ 50g ai / ha foliar spray, which can effectively control Colorado potato beetle, diamondback moth, Trichoplusia moth, Mexican boll weevil and flower thrips. Paddy fields using 50 ~ 100g ai / ha can be a good control borers, brown planthopper and other pests. 6 ~ 15g ai / ha foliar spray, can prevent prairie and desert locust locust genus genus pests. 100 ~ 150g ai / ha applied to the soil, can effectively control corn rootworm, wireworms and cutworms. 250 ~ 650g ai / 100 kg of maize seed seed treatment, can effectively control corn wireworms and cutworms. The main object of this product include prevention of aphids, leafhoppers, caterpillars, flies and other pests Coleoptera. Is recommended as the first choice of many varieties of pesticide experts instead of highly toxic organophosphorus pesticides.
Gibberellic acid use
1 to promote the formation of fruit or fruit seedless cucumber flowering period with 50-100mg / kg liquid spray a Conference on Facilitating the fruit, increase. 7-10 days after flowering grapes, muscat grapes with 200-500mg / kg liquid spray ear 1, to promote non-stone formation.
2 celery promote vegetative growth before harvesting two weeks with 50-100mg / kg liquid spray leaves 1; 3 weeks before harvest spinach leaf spray 1-2 times, can stem increases.
3 break dormancy promote sprouting of potatoes before sowing with 0.5-1mg / kg liquid immersion tubers 30min; former big Maibo with 1mg / kg soaking liquid, can promote germination.
4 anti-aging and Preservation garlic with 50mg / kg of liquid garlic dip base 10-30min, green citrus fruit with 5-15mg / kg liquid spray fruit 1, after the banana harvest with 10mg / kg liquid dip fruit , cucumber, watermelon harvest before using 10-50mg / kg liquid spray melons, can play a role in preservation.
5 regulate flowering chrysanthemums vernalization stage with 1000mg / kg liquid spray leaves, cyclamen bud stage with 1-5mg / kg liquid spray can promote flowering buds.
6 seed rate of hybrid rice seed production is generally heading in the beginning of 15% female, 25% heading to the end of treatment 1-3 times with 25-55mg / kg liquid spray. First with a low concentration, the high concentration.

Glyphosate use and usage
The original drug use: can be used for processing into 10% glyphosate, 41% Glyphosate IPA, 62% Glyphosate IPA.
Preparation purposes:
Uptake and broad-spectrum Herbicide. The main body of the enol acetone inhibit plant-based shikimene phosphate synthase, thereby inhibiting the conversion shikimene to phenylalanine, tyrosine and tryptophan, the protein synthesis is disturbed, leading to plant death.
Initially used in rubber plantations controlling thatch and other weeds, can advance a year tapping rubber trees, old rubber tree production. Now gradually extended to forestry, orchards, mulberry, tea, rice and wheat, rice and rapeseed rotation land. Various weeds different sensitivity to glyphosate, which dosage is different. Such as barnyardgrass, green foxtail, foxtail, goosegrass, crabgrass, cleavers and other annual weeds, the dosage of the active ingredient is counted as 6 ~ 10.5 g / 100m. On Plantago, small canadensis, and other dosage Commelina as an active ingredient for 11.4 ~ 15g / 100m. Right Imperata, bony grass, reeds, etc. need 18 ~ 30g / 100m, generally water 3 ~ 4.5kg, directed spray evenly on weed stems.
Usage:
Controlling apple orchard, Taoyuan, vineyards, pear, tea, mulberry and farmland fallow weed, barnyard weed, foxtail, goosegrass, crabgrass, cocklebur, pigweed, chickweed, cleavers and other annual weeds.

Methomyl Caution
HAZARDS
Health hazards: mainly cholinergic crisis. The main symptoms include salivation, lacrimation, blurred vision, tremors, convulsions, delirium, coma, nausea, vomiting, diarrhea, abdominal pain, and finally respiratory failure and death.
Environmental hazards: hazard to the environment, water and soil pollution.
Explosion hazard: The product flammable, highly toxic.
First aid measures
Skin contact: Remove contaminated clothing, rinse with plenty of water.
Eye contact: Did eyelid, mobile water rinse or saline. Medical treatment.
Inhalation: rapidly from the scene to fresh air. Keep the airway open. If breathing is difficult, give oxygen. If not breathing, give artificial respiration immediately. Medical treatment.
Ingestion: drink plenty of water, induce vomiting. Gastric lavage, catharsis. Medical treatment.
Fire-fighting measures
Hazardous characteristics: case of fire, combustible high fever. Heating decomposition and emit nitrogen, sulfur oxides and other toxic gases.
Hazardous combustion products: carbon monoxide, carbon dioxide, nitrogen oxides, sulfur oxides.
Fire fighting methods: firefighters are required to wear gas masks, at a safe distance, the wind on fire.
Extinguishing Media: Water spray, foam, dry powder, carbon dioxide, sand.
Spill response
Emergency treatment: isolation leak contaminated areas, restricting access. Cut off the fire source. Recommended emergency personnel wearing self-Pressurized respirators to wear protective clothing. Clean shovel collection in a dry, clean, covered containers, transferred to a safe place. You can also rinse with plenty of water, wash water diluted into the wastewater system. If large spills, recycling or collection shipped to the waste disposal sites.

Oxamyl – Transport Information
Transportation Note: Transport containers should be preceded by check is complete, seal, transport process to ensure that the container does not leak, did not fall, do not fall, no damage. Prohibited and acids, oxidants, food and food additives mixed operation. Transport vehicles should be equipped with the appropriate variety and quantity of fire equipment and emergency equipment leakage during transport. Transit should prevent exposure, rain, high temperature. According to the provisions road transport routes, not in residential areas and densely populated areas.
Triclosan chemical products
In the United States, triclosan is mainly produced by Ciba Specialty Chemicals (Ciba Specialty Chemicals) American factories, the company uses Irgasan DP300 (triclosan new DP300) as a trade name. In China, a major manufacturer of triclosan Tianjin Braun disinfectant limited liability company [5], are generally used directly as a trade name of triclosan.
In other countries and regions, triclosan usually have some of the following trade names:
CH-3565 triclosan CH 3635 Irgasan Ch 3635 Irgasan DP 300 Lexol 300 Ster-Zac.
TCS triclosan triclosan triclosan Jamie Dawson of the TU pure new antibacterial triclosan new DP300 Wei Wei Jie Jie Ling -100 pure.
Specifications
Product Specifications:
Content ≥99% Melting point 93-98 ℃.
Color gray or white crystals Loss on drying ≤0.5%.
Residue on ignition ≤0.1% Heavy metals ≤20PPM.
Role
Triclosan is widely used for efficient medicated soap (hygiene soap), health lotion), in addition to underarm (foot aerosol), hand sanitizer, wound disinfectant sprays, medical disinfectants, hygiene cleanser (cream), air fresheners and refrigerator deodorant, but also for the health embalmed fabric finishing and plastics, higher purity Chris grace is also widely used in the treatment of gingivitis, periodontitis and oral ulcers efficacy of toothpaste and mouthwash, recommended concentration of 0.05% to 0.3%.

Sodium thiosulfate purposes Profile
When tanning dichromate reducing agent, nitrogen exhaust neutralizer, mordant, straw and
Hair bleach and bleach pulp dechlorination time. Also for tetraethyl lead, dyes intermediates manufacturing and silver ore mention reducing electroplating industry, water purification works purifying agent.
In the textile industry for bleaching cotton after dechlorination agent, sulfur dyed wool fabric dye, indigo dye anti-white agents, pulp dechlorination agent, the pharmaceutical industry as detergents, disinfectants and fading agents. [3] analytical reagent for chromatography reagents, drip Determination of cobalt, photographic fixer, dechlorination agent capacity analysis commonly used reagents, sodium, preparation of injectables and double sugar iron urea medium mordant.
Sodium thiosulfate and cyanide may also be used as a detoxifying agent.
The main purpose of sodium fluoride
Phosphate coating industry for the accelerator, so that stable phosphate solution, phosphate refinement, improved phosphate coating performance. Aluminum and its alloys phosphate in great danger of closure has a negative catalytic Al3 +, so phosphide smooth wood preservatives, agricultural pesticides, fungicides brewing industry, pharmaceutical preservatives, welding flux, alkaline zinc zinc salts additives and enamel, paper and so on.
Butylparaben use
Catalytic Synthesis of a sulfuric acid, butyl paraben
Sulfuric acid catalyzed esterification method is the classic method of synthetic esters, synthetic parabens, the hero Hasegawa, Atsushi Maekawa governance and Xie Wei Yang and has long been reported. Such a catalytic reaction for a long time, low yield, alcohol consumption, and improve the use of p-hydroxybenzoic acid, n-butanol, benzene and sulfuric acid molar ratio of 1: 3.5: 1: 0.015, refluxing 1 h , n-butyl paraben yield up to 99.12%, with an average yield of 97.58%.
Ming et al pipe coil in toluene as the solvent, when p-hydroxybenzoic acid, n-butanol and toluene molar ratio of 1: 4: 2, with sulfuric acid as a catalyst, refluxing 4 h, then the solvent was distilled off and 50% alcohol, cooling precipitation precipitation, filtration, n-butyl paraben was 89.3% yield. Zhengxue Zhong et without organic solvent with n-butanol as a dehydrating agent, p-hydroxybenzoic acid, n-butanol and sulfuric acid molar ratio of 1: 3.5: 0.15, refluxing 0.75 h, p-hydroxybenzoate n-butyl formate yield of 98.4%.
To improve the storage and ease of use, tubes and the like to the disc-ming sulfate SO4 2- / bentonite catalyst (mass fraction of about 5%), with toluene as the solvent, when p-hydroxybenzoic acid, n-butanol and toluene molar ratio of 1: 4 : 2, in the <110 ℃ stirred refluxing 5h, then steamed out 50 percent of solvents and alcohol, cooled to precipitate precipitation, filtration to obtain the product of n-butyl paraben, yield 88.6%.
To accelerate the reaction process under microwave irradiation synthesis of n-butyl paraben, when p-hydroxy benzoic acid, n-butanol molar ratio of 1: 4, the use of sulfuric acid as a catalyst in the working frequency of the microwave radiation source 2450MHz 30min, n-butyl paraben yield of 85.1%, rather than use the microwave, you need to refluxing 300min, product yield was 83.8%, so the reaction rate increased by 10-fold.
2 sulfonic acid catalytic synthesis of butyl paraben
2.1 p-toluenesulfonic acid
Since the sulfuric acid cause side reactions when heated organic etherification, oxidation, carbonization, sulfonation, while its corrosion resistance, operation, use and storage is not convenient and safe. Toluenesulfonic acid (p-CH3C6H4SO3H.H2O) is an organic acid, sulfuric acid can overcome many shortcomings, easy to use, is a good catalyst for esterification, can be synthesized in high yields of hydroxy esters. The author has used 0.05mol paraben, 0.30mol alcohol in 0.0052mol (1.0g) under refluxing toluene sulfonic acid catalysis 3h, n-butyl paraben yield of 95.9% . Since the p-toluenesulfonic acid dissolved in an organic reaction system, the reaction liquid after the reaction the acid is still strong, the need for treatment, there is a certain waste liquid, the catalyst can not be reused. Shi Lei, such as 10g of granular activated carbon immersed in 60mL mass fraction of 25% aqueous solution of toluene sulfonic acid 30h, drained after too 15.31g, immobilization rate of 53.10%, select this catalyst 0.6g, 0.1mol hydroxybenzoic acid, 0.3mol butanol refluxing 3h, n-butyl paraben yield of 98.02%, the catalyst can be reused five times, the yield was still up 97.65% [9 ]. This method is easy to operate, reducing environmental pollution, high ester yield, catalyst reuse performance, is a good catalyst.
2.2 amino acid
Sulfamic acid (H2N-SO2OH) with p-toluenesulfonic acid, as is also an inexpensive, readily available, stable solid. Transport, storage, easy to use, except that it is insoluble in organic reaction system, easy separation, can be reused, for small equipment corrosion, high yield synthesis products is a good catalyst for the synthesis of butyl paraben. When the right-hydroxy acid, n-butanol and the amino acid molar ratio of 1: 4: 0.41 refluxing 3h, n-butyl paraben yield of 97.9%. When converted to butanol isobutanol, p-hydroxybenzoic acid, isobutyl alcohol, an amino acid molar ratio of 1: 6: 0.52 refluxing 3h, p-hydroxybenzoic acid yield of 90.7 Isobutyl %.
2.3 strong acid cation exchange resin
Strong acid cation exchange resin is a polymer acid, cheap, no corrosion of equipment, do not pollute the environment, does not cause side effects, and the resin is insoluble in the reaction system, recyclable, recycled and reused, easy to operate , product yield, is an effective catalyst for industrial production. Using five kinds of models of the resin (D72, D61, dry hydrogen resin, HD-8 and JK008) catalytic synthesis of ethyl paraben, Discovery JK008 resin highest activity. When the p-hydroxybenzoic acid to the resin mass ratio of 1: 0.08, p-hydroxybenzoic acid with n-butanol molar ratio of 1: 5.5, refluxing 4.5h, obtained by gas chromatographic analysis of n-butyl p-hydroxybenzoate ester yield of 98.0%, JK008 resin has good reuse catalytic performance.
Introducing benzene sulfonic acid groups on the benzene ring zirconium, made a similar strong acid cation exchange resin solid acid – acid sulfonated benzene zirconium (ZSPP), catalytic synthesis of n-butyl paraben. Specific conditions: 0.05mol paraben, 0.20mol n-butanol, 1g ZSPP catalyst at 117¯120 ℃ refluxing 8 h, n-butyl paraben yield of 92%, this catalyst can reuse reused 10 times, the yield is still about 90%, the catalyst has a high thermal stability (over 250 ℃ was released SO2) than the sulfonic acid resin, an organic substance at high temperature coking, no corrosion of equipment application prospect is a solid acid catalyst promising.
3 Catalytic Synthesis of inorganic salts and oxides of butyl paraben
Catalytic and catalytic sulfuric acid were discussed earlier proton acid catalysis, catalytic inorganic salts and oxides vary due to different compounds. There are a large class of inorganic materials is cheap and easy to get the Lewis acid, the metal atom has with the carboxylic acid carbonyl oxygen ligands empty track, which has catalyzed esterification, while their small equipment corrosion, pollution reduction, catalyst with less, is a good catalyst for the synthesis of certain esters. Iron (Ⅲ) electronegativity strong, Fe3 + in outer space orbit with the carboxylic acid carbonyl oxygen ligands. Liu Yong, etc. using Fe2 (SO4) 3 · xH2O catalytic synthesis of n-butyl paraben: 0.1mol paraben, 0.4mol n-butanol, 0.5g of the catalyst under refluxing 4h, acid conversion rate of 91.6%, after going alcohol, after recrystallization paraben, n-butyl ester yield of 85% fine. Acetate Catalyzed, who used hydroxybenzoic acid and n-butanol molar ratio of 1: 4 to 4% of the mass fraction (based on the total reactant meter) chloride as catalyst different refluxing 5 h, then the catalyst was filtered off, the alcohol is recovered by distillation, the crude ester are precipitated by the water, an alkali, washed with water, then ethanol – n-butyl p-hydroxybenzoate may, after finishing the water of crystallization yield of an ester, respectively:
Catalyst CaCL2 ZnCL2 FeCL3 · 6H2O ALCL3 · 6H2O
Ester yield /% 30307883
Thus, chloride has a catalytic role, especially FeCl3 · 6H2O and AlCl3 · 6H2O is a good catalyst for the synthesis of the esters. Previously, Zhang Jing Qing, who have also been reported: When right-hydroxy acid with n-butanol molar ratio of 1: 3.5, FeCl3 · 6H2O mass fraction (the total mass of reactants) of 5%, in 139¯ under 140 ℃ reaction 1.5h, 84.6% of the available yield of n-butyl paraben [17]. Wang Mingxing, etc. have also been studied: when hydroxybenzoic acid, n-butanol and FeCl3 · 6H2O molar ratio of 1: 2: 0.12 refluxing 3h, the yield of n-butyl paraben 95 .1% ¯96.3% [18]. Yao spring, also reported the catalytic effect of FeCl3 · 6H2O, in its optimum conditions, product yield was 98.9%.
Tin (II) is also high negative elements, such as the use of cost Prudential stannous oxide (SnO) as catalyst was successfully synthesized n-butyl paraben: 0.1mol paraben, 0.3mol n-butanol . 5gSnO, 140 ℃ refluxing 4h, acid conversion rate of 96%.
Since most of the inorganic chlorides hygroscopic and difficult to use and accurate storage, and they were dissolved in the reaction system, to the product separation and purification inconvenience. Ammonium ferric sulfate is a stable crystal, in addition to having the chloride advantages, it is not easy to absorb moisture, insoluble in the reaction system, the reaction to form a loose spherical solid, non-corrosive reaction equipment, is a good ester catalyst. Deng Xuzhong such as the use of its catalytic synthesis of n-butyl paraben: 0.1mol paraben, 0.35mol n-butanol, 1.0g catalyst refluxing 4 h, the crude ester yield of 93.7% , after recrystallization from ethanol the yield was 90.1% fine ester.
Li Xiaoli, such as the use of rare earth oxide, neodymium oxide (Nd2O3) catalytic synthesis of n-butyl paraben, its optimal reaction conditions: When right-hydroxy acid, n-butanol molar ratio of 1: 4, the amount of catalyst of 5% by mass of p-hydroxybenzoic acid, refluxing 4h, yield of the ester was 81.2% and the good catalytic effect is repeated, the method to reduce the corrosion of equipment and environmental pollution, has certain industrial value.
Catalytic inorganic discussed above is part of Lewis acid catalysis. The authors note monohydrate sodium bisulfate (NaHSO4 · H2O) is also a good esterification catalyst, inexpensive, readily available, and stable crystal properties, and its solution is strongly acidic, due to ionizing HSO4- have H + exists, belongs to the proton acid catalysis, capable of catalyzing the synthesis of butyl paraben: When hydroxybenzoic acid, n-butanol and sodium hydrogen sulfate monohydrate molar ratio of 1: 2: 0.072 when refluxing 5h, n-butyl paraben ester yield of 92.8%; when paraben, isobutyl alcohol and sodium hydrogen sulfate monohydrate molar ratio of 1: 3: 0.036 refluxing 7h, isobutyl paraben yield can also be 99%. Of microwave radiation sodium bisulfate next catalytic synthesis of butyl paraben work, the optimization of reaction conditions: when n (alcohol): n (acid): n (NaHSO4 · H2O) = 0.15: 0 .05: 0.058, using the power of 210W microwave radiation 28min, product yield was 93.6%. The catalyst and the reaction time is shortened, the remaining sodium bisulfite and has a repetitive catalytic performance due to their insoluble in the reaction system, the corrosion of the equipment is greatly reduced, there is a catalyst for industrial application.

