HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fenazaquin
el436 · MAGISTER · XDE 436) · FENAZAQUIN · phenethoxy) · AFenazaquin · Fenazaquin 0.1 · 4-(4-(tert-Butyl)
Identifiers & Physical Properties
| CAS No. | 120928-09-8 |
|---|---|
| Molecular formula | C20H22N2O |
| Average molar mass | 306.4 g/mol |
| Monoisotopic mass | 306.17321332 g/mol |
| SMILES | CC(C)(C)c1ccc(CCOc2ncnc3ccccc23)cc1 |
| InChIKey | DMYHGDXADUDKCQ-UHFFFAOYSA-N |
| PubChem CID | 86356 |
| ChEMBL | CHEMBL243282 |
| ChEBI | CHEBI:38593 |
| EC No. | 410-580-0 |
| DTXSID | DTXSID4040476 |
Chemical & Physical Properties
| XLogP | 5.7 |
|---|---|
| Topological polar surface area | 35 |
| Hydrogen bond donors | 0 |
| Hydrogen bond acceptors | 3 |
| Rotatable bonds | 5 |
| Heavy atoms | 23 |
| Formal charge | 0 |
| Complexity | 357 |
| Pesticides | AcaricidesActive substance -> EU Pesticides database: ApprovedEnvironmental transformation -> Pesticides (parent, predecessor)Acaricides, InsecticidesPesticide (Fenazaquin) -> USDA PDB |
| LogP (partition coefficient) | log Kow = 5.51 at 20 °C4.91 |
| Density | 1.161.0970 (rough estimate) |
| Color/Form | Colorless crystals |
| Solubility | In acetone, hexane 33-50, acetone, ethyl acetate 400-500, n-chlorobutane, chloroform, toluene, N-methyl-2-pyrrolidone >500, dichloromethane >600, dimethylformamide 300-400, ethylene glycol <5, isopropanol, methanol 50-100 (all in g/L at 23 °C)In water, 0.102 mg/L (pH 5, 7) , 0.135 mg/L (pH 9)both at 20 °CChloroform (Slightly), Ethyl Acetate (Slightly)0.102 mg l-1 (20 °C, pH 7) |
| Endocrine Disruptors | Potential endocrine disrupting compound |
| Decomposition | When heated to decomposition it emits toxic fumes of /nitrogen oxides/. |
| Melting point | 77.5-80 °C70-71° (Dreikorn)mp 77.5-80.0° (Gambie) |
| Vapor pressure | 3.4X10-3 mPa /2.55X10-8 mm Hg/ at 25 °C3.4 x l0-6 Pa (25 °C) |
| Stability/Shelf Life | DT50 of aqueous solution exposed to sunlight is 15 days (pH7, 25 °C) |
| Dissociation Constants | pKa = 2.44 |
| Boiling point | 447.01°C (rough estimate) |
| Refractive index | 1.5700 (estimate) |
| Storage conditions | Sealed in dry,Room Temperature |
| pKa (acidity coefficient) | 2.88±0.30(Predicted) |
| Physical state | solid |
| Color | White to off-white |
| BRN | 8331263 |
| Henry's law constant | 2.1×102 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) |
| Major applications | agricultureenvironmental |
| InChI | 1S/C20H22N2O/c1-20(2,3)16-10-8-15(9-11-16)12-13-23-19-17-6-4-5-7-18(17)21-14-22-19/h4-11,14H,12-13H2,1-3H3 |
| InChIKey | DMYHGDXADUDKCQ-UHFFFAOYSA-N |
| SMILES | CC(C)(C)c1ccc(CCOc2ncnc3ccccc23)cc1 |
| LogP (partition coefficient) | 5.510 |
| CAS DataBase Reference | 120928-09-8(CAS DataBase Reference) |
| FDA UNII | DK5Q534WEE |
| EPA Substance Registry System | Fenazaquin (120928-09-8) |
| UNSPSC Code | 41116107 |
| NACRES | NA.24 |
| GHS pictogram | GHS06,GHS09 |
| Signal word | Danger |
| GHS hazard statements | H301-H332-H410 |
| GHS precautionary statements | P261-P264-P270-P273-P301+P310-P304+P340+P312 |
| Personal protective equipment (PPE) | dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
| Hazard symbols | T,N |
| Risk statements (R) | 20-25-50/53 |
| Safety statements (S) | 37-45-60-61 |
| UN transport number | UN 2811 6.1/PG 3 |
| Water hazard class (WGK) | 3 |
| RTECS number | VA1382000 |
| Storage class | 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects |
| Hazard class | Acute Tox. 3 OralAcute Tox. 4 InhalationAquatic Acute 1Aquatic Chronic 1 |
| Hazardous substances data | 120928-09-8(Hazardous Substances Data) |
| Toxicity | LD50 orally in rats, mice (mg/kg): 134, 1480dermally in rabbits (mg/kg): >5000LC50 (96 hr) in bluegill, trout (mg/l): 34.1, 3.8 (Longhurst) |
| REACH registrations | Inactive |
Safety & Regulations
| GHS classification | DangerH301: Toxic if swallowed [Danger Acute toxicity, oral]P261, P264, P270, P271, P273, P301+P316, P304+P340, P317, P321, P330, P391, P405, and P501 (click each P-code to see the statement)H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral] |
|---|---|
| Regulatory information | Regulation (EC) No 1107/2009 (amended)Fenazaquin is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)2011/39/EU, Reg. (EU) 2023/918, Reg. (EU) No 2018/1266, Reg. (EU) No 2018/690, Reg. (EU) No 540/2011Status: Active Update: 15-12-2008 https://echa.europa.eu/registration-dossier/-/registered-dossier/3270Quinazoline, 4-2-4-(1,1-dimethylethyl)phenylethoxy-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right. |
| Special Reports | USEPA Office of Prevention, Pesticides and Toxic Substances, Pesticide Fact Sheet for Fenazaquin (August 2007).[Available from, as of June 1, 2011: http://www.epa.gov/opprd001/factsheets/] |
| FIFRA requirements | Import tolerances are established for residues of the insecticide and miticide, fenazaquin, 4-tert-butylphenethyl quinazolin-4-yl ether, in or on raw agricultural commodities as follows: [Table#7848] |
| Hazard Classes and Categories | Acute Tox. 3 (100%)Hazardous to the aquatic environment (acute) - category 1Acute Tox. 3 * |
| Disposal methods | SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air qualitypotential migration in soil or watereffects on animal and plant lifeand conformance with environmental and public health regulations. |
| Allowable Tolerances | Import tolerances are established for residues of the insecticide and miticide, fenazaquin, 4-tert-butylphenethyl quinazolin-4-yl ether, in or on raw agricultural commodities as follows: [Table#7847] |
| Ecotoxicity values | LD50Species: Colinus virginianus (Northern Bobwhite Quail, age approximately 18 weeks, 208 g initial bw range 201-208 g) gavage, 1747 mg/kg bw for 19 days (95% confidence interval: 1508-2176 mg/kg)LC50Species: Colinus virginianus (Bobwhite quail) diet >5204 ppm for 5 days /98.4% a.i./Species: Anas platyrhynchos (Mallard duck) oral >2000 mg a.i./kg bw /98.4% a.i./Species: Anas platyrhynchos (Mallard duck) diet >5030 ppm for 5 days /98.4% a.i./For more Ecotoxicity Values (Complete) data for Fenazaquin (13 total), please visit the HSDB record page. |
| Environmental fate | TERRESTRIAL FATE: Based on a classification scheme(1), Koc values of 18700 to 42100(2) indicate that fenazaquin is expected to be immobile in soil(SRC). Volatilization of fenazaquin from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.0X10-7 atm-cu m/mole(SRC), based upon its vapor pressure, 2.55X10-8 mm Hg(3), and water solubility, 0.102 mg/L(3). Fenazaquin is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). The half-life in soil is approximately 45 days(3).AQUATIC FATE: Based on a classification scheme(1), a Koc range of 18700 to 42100(2) indicates that fenazaquin is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 1.0X10-7 atm-cu m/mole(SRC), derived from its vapor pressure, 2.55X10-8 mm Hg(4), and water solubility, 0.102 mg/L(4). According to a classification scheme(5), a BCF of 500(2) suggests that bioconcentration in aquatic organisms is high, provided the compound is not metabolized by the organism(SRC). The half-life of an aqueous solution exposed to sunlight is 15 days at pH 7, 25 °C(4). Biodegradation data in water were not available(SRC, 2011).AQUATIC FATE: Using an aquatic microcosm study simulation of 5% drift and 1% runoff from agricultural fields, fenezaquin was applied at rates of 225, 440, and 1125 g active ingredient/ha. After 2 hours, fenazaquin concentrations in a model pond were 0.58, 1.07, and 2.68 ug/L, respectively. Over 22 hours, concentrations dropped by 60-70%. No fenazaquin was detected in the water after 21 days(1).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), fenazaquin, which has a vapor pressure of 2.55X10-8 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase fenazaquin may be removed from the air by wet or dry deposition(SRC). Fenazaquin contains chromophores that absorb at wavelengths >290 nm(4), and therefore may be susceptible to direct photolysis by sunlight(SRC). |
| Ecotoxicity excerpts | /BIRDS and MAMMALS/ Reproduction studies conducted with bobwhite quail and rats indicate no frank reproductive effects in either birds or mammals. In the avian reproduction study, the only observed effect was on growth in males at the highest concentration tested /(953 ppm for 22 weeks)/ /98.0% AI//AQUATIC SPECIES/ Rainbow trout (Oncorhynchuys mykiss) /were studied in a/ 63-day early life stage /experiment under/ unaerated continuous flow /conditions/. 80 embryos/concentration level. 0, 0 (solvent), 0.20, 0.51, 0.96, 1.98 and 3.92 mg/L. NOAEC: 0.96 ug/L LOAEC 1.98 ug/L. At test termination, survival, body weight and body length were significantly reduced at 1.98 ug/L. No fish survived at 3.92 ug/L. Excessive analytical variation (> or =20% of the mean measured value) at the three lowest levels, which included the NOAEC levelsolvent level not constanttest initiation was with eyed-embryos (e.g., the exposure period was too short) and no time to swim-up assessment. /98% a.i. technical fenazaquin/ /from table//AQUATIC SPECIES/ In a 96 hr acute toxicity study, rainbow trout (/Oncorhynchus mykiss/) were exposed to EL-436 (fenazaquin) at nominal concentrations of 0 (negative and solvent controls), 2.5, 5.0, 7.0, 8.5 and 10.0 ug/L under flow-through conditions. TWA concentrations (reviewer-calculated) were <1 (<LOQ, controls), 1.6, 3.0, 4.4, 5.4, and 8.8 ug a.i./L, respectively. the 96-hr LC50 (with 95% CI) was 3.9 (3.0-5.4) ug a.i./L. The NOAEC, based on treatment-related mortality and signs of toxicity, was 3.0 ug ai/L. Sublethal effects (sluggishness, hypoactivity, or prostration) were observed in surviving fish from the 4.4 ug ai/L level from 24 to 48 hours. Based on the results of this study, EL-436 (fenazaquin) would be classified as very highly toxic to juvenile rainbow trout in accordance with the classification system of the USEPA./AQUATIC SPECIES/ The 48 hr acute toxicity of EL-436 (fenazaquin) to Daphnia magna was studied under static conditions. Daphnids (30 organisms/level) were exposed to EL-436 at nominal concentrations of 0 (control and solvent control), 0.3, 1.0, 3.0, 4.5, 7.0, and 10.0 ug/L. Mean measured concentrations of fenazaquin were <0.2 (<LOD, controls), 0.3, 0.8, 3.0, 4.4, 6.8, and 9.8 ug ai/L, respectively. Following 48 hr of exposure, cumulative immobility was 4% in the negative control group, 13% in the solvent control group, and 0, 7, 20, 23, 83, and 100% in the mean-measured 0.3, 0.8, 3.0, 4.4, 6.8, and 9.8 ug ai/L treatment groups, respectively. The 48-hr EC50 (with 95% CI) for immobility was 5.6 (5.0-6.3) ug ai/L. Hypoactivity or prostration was also observed at the > or =3.0 ug ai/L exposure levels. The NOAEC for immobility and the other sublethal observations was 0.8 ug ai/L. Based on the results of this study, EL-436 (fenazaquin) would be classified as very highly toxic to Daphnia magna in accordance with the classification system of the USEPA. |
| Soil Adsorption/Mobility | The Koc of fenazaquin has been reported to range from 18700 to 42100(1). The compound is rapidly adsorbed onto soil particles with 88% and 96% of the adsorption from a sandy loam soil and a clay loam soil, respectively, occurring within 2 hours. Adsorption increases with the organic content and clay content(1). According to a classification scheme(2), this Koc range suggests that fenazaquin is expected to be immobile in soil. |
| Artificial Pollution Sources | Fenazaquin's production may result in its release to the environment through various waste streamsits use as an acaricide(1) will result in its direct release to the environment(SRC). |
| Environmental Bioconcentration | A BCF range of 500 was measured in fish for radio-labeled fenazaquin, at a concentration of 0.02 and 0.01 ug/L, using rainbow trout (Oncorhynchus mykiss) exposed for 21 to 28 days. BCF values were 400-500 for days 1-2 and 400-600 on days 21-28, irrespective of initial test compound concentration. At the end of the depuration period (days 1 and 14) no radioactivity was detected in the water above the detection limit of 0.05 ug/L. Residues in fish fell rapidly with 80% of radioactivity eliminated within the first 24 hours, <7% remaining on day 7. The depuration half-life was 1.4 days over days 1-7(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is high(SRC), provided the compound is not metabolized by the organism(SRC). |
| Volatilization from Water/Soil | The Henry's Law constant for fenazaquin is estimated as 1.0X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 2.55X10-8 mm Hg(1), and water solubility, 0.102 mg/L(1). This Henry's Law constant indicates that fenazaquin is expected to be essentially nonvolatile from water and moist soil surfaces(2). Fenazaquin is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1). |
| Non-Human Toxicity Excerpts | /LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ In a 90-day oral toxicity study, XDE-436 (/fenazaquin/ 98.1% ai) was administered to 4 Beagle dogs/sex/dose in diet at dose levels of 0, 1, 5, or 15 mg/kg bw/day at constant dosing. All percentages presented are changes from controls. No toxicological effects on organ weight, clinical chemistry, clinical signs, hematology, gross and histopathology were related to the dietary exposure of fenazaquin to beagle dogs. At 15 mg/kg/day dose, significant reductions in body weight of males (6 to 12%) and females (4 to 11%) were reported. At the high dose, overall body weight gain decreased in males (76%) and females (73%)mean food consumption was reduced in males (6 to 24%) and females (10 to 27%). Food efficiency values were also significantly decreased in high dose groups, males (72%) and females (67%). ... The toxicologically significant body weight changes correspond to the decrease in food consumption reported for the high dose group, which appears to be due only in part to a reduction in palatability of the diet. Based on the toxicological findings associated with fenazaquin 90-day dietary exposure to beagle dogs, the NOAEL is established at 5 mg/kg/day and the LOAEL is established at 15 mg/kg/day based on reductions of body weight, body weight gain, food consumption and food efficiency./LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ In a 90-day oral toxicity study EL-436 (/fenazaquin/ purity 98%) was administered to 15 Syrian golden hamster [Lak:LVG(SYR)]/sex/dose by gavage at doses of 0, 5, 25, 75, or 150 mg/kg/day for males and 0, 5, 25, 50, or 100 mg/kg/day for females. Control animals received 5 mL/kg of the vehicle (10% aqueous acacia solution). There were no treatment related mortalities or clinical signs and no difference between the controls and the fenazaquin treated groups in urinalysis. Food consumption data from the first 10- weeks of the study were considered unreliable due to excessive spillage. There were slight dose-related increases (22-69%) in liver microsomal p-nitroanisole-o-demethylase enzyme activity in all animals that received fenazaquin at > or = 25 mg/kg/day but no changes were seen in hepatic peroxisomal beta-oxidation activity (fatty acyl CoA oxidase). Small changes occurred in some hematology parameters (< or = 6% decrease) among treated hamsters but, the changes were within the normal ranges of biological variation and were not considered toxicologically meaningful. The greatest effect of treatment was on body weight. At termination, the body weight in males decreased (p<0.01) 16 and 23% relative to the controls in the 75 and 150 mg/kg/day groups. Similarly, body weight in females decreased (p<0.01) 19 and 28% relative to the controls in the 50 and 100 mg/kg/day groups, respectively. The body weight gains from the same treated groups were also substantially reduced 54 and 74% less than the controls in males and 39 and 61% less than the controls in females, respectively. Because of growth retardation, the absolute organ weights of kidney, heart, and spleen were decreased in animals at dose levels > or = 50 mg/kg/day. The large decrease in absolute (42-49%) and relative weights (27-36%) of testes and prostate are considered treatment-related in males administered 75 and 150 mg/kg/day fenazaquin. These findings are corroborated by histopathology findings of increased testicular hypospermatogenesis (0/15, 1/15, 2/15/, 5/15/ and 8/15 in control through the high dose groups, respectively, moderate to severe at the top two doses). Under the conditions of the study, the LOAEL for fenazaquin in male hamsters is 75 mg/kg/day based on decreased body weight, reduced testes and prostate weights, and testicular hypospermatogenesis. The LOAEL is 50 mg/kg/day in females based on decreased body weight. The NOAEL for EL-436 is 25 mg/kg/day for both males and females./LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ In a 90-day oral toxicity study EL-436 (fenazaquin98.4% ai) was administered to 10 Fischer 344 rats/sex/dose in the diet at dose levels of 0.0%, 0.0015%, 0.0045%, 0.015%, or 0.045% (equivalent to 0.0, 1.0, 3.0, 9.6, and 28.7 mg/kg bw/day for males and 0.0, 1.2, 3.5, 11.5, and 33.0 mg/kg bw/day for females, respectively). All rats survived to scheduled termination, and no treatment-related clinical signs were noted. In the high dose group, body weight of males was significantly reduced by 10-14% throughout the study, and overall body weight gain was reduced by 21%. Body weight of high dose females was significantly reduced by 5-7% during most of the study, and overall body weight gain was reduced by 14%. Food consumption by the high dose males and females was significantly reduced by 10 to 21% throughout the study, and overall food consumption was reduced by 14% and 11%, respectively, compared to that of the controls. Food efficiency in the high dose males was significantly reduced by 16% at week one and by 8% at study endfood efficiency for all other treated groups was comparable to that of controls. Hematology results for all groups were unremarkable. Changes in clinical chemistry included increased serum enzyme activities (61-75% over controls) in the high dose males and increased hepatic microsomal enzyme activities (21-80%) in mid- and high-dose males and females. Due to a lack of histological correlates and minimal increases in liver weight, these changes in isolation are considered an adaptive response rather than a toxic effect. Urinalysis was unremarkable. Changes in absolute organ weight in the mid- and high-dose groups were generally less than 10%, and not considered biologically significant. Increased relative organ weights (7-17% over controls) for those groups reflected the decreased body weights. No histological correlates were seen for the organ weight changes. Gross pathology was unremarkable, and no treatment-related histopathologic changes were seen. The LOAEL for fenazaquin in rats is 0.045% in the diet (28.7 mg/kg bw/day for males and 33.0 mg/kg bw/day for females) based on decreases in body weight, body weight gain, and food consumption. The NOAEL is 0.015% in the diet (9.6 mg/kg bw/day for males, 11.5 mg/kg bw/day for females)./LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ In a 90-day oral toxicity study, EL-436 (/Fenazaquin/ > or = 99% ai) was administered to 15 F344 rats/sex/dose group daily by gavage at dose levels of 0, 1, 3, 10, or 30 mg/kg/day for 90 days. In addition, 10 rats/sex in the control and high-dose groups were maintained 1-month post treatment to evaluate the reversibility of observed effects. There were no compound related effects on survival, clinical signs, ophthalmic, hematologic, or urinary parameters. Statistically significant decreases in body weight (8%-12% in males) and body weight gain (18% and 13% in males and females, respectively) were noted only among high-dose rats. The high dose also resulted in a statistically significant decrease in food consumption (4%-8%) and food efficiency (10% and 12%) in both sexes. Following a recovery period these parameters returned to normal. Slight changes in clinical chemistry parameters observed in high dose male and female rats were reversible 1-month post treatment. Statistically significant increases in absolute and relative liver and adrenal weight in mid- or high-dose male and female rats (6%-20% for liver and 10%-42% for adrenal, respectively) observed during the treatment period were reversible during the post treatment period. However, these findings were not supported by histopathological changes. Changes in serum enzyme activity levels and liver weight were considered adaptive changes in response to the treatment. The LOAEL for EL-436 in male and female rats is 30 mg/kg/day based on decreases in body weight gain, food consumption and food efficiency in both sexes. The NOAEL is 10 mg/kg/day.For more Non-Human Toxicity Excerpts (Complete) data for Fenazaquin (16 total), please visit the HSDB record page. |
| Environmental Abiotic Degradation | Fenazaquin is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(1). Fenazaquin contains chromophores that absorb at wavelengths >290 nm(1), and therefore may be susceptible to direct photolysis by sunlight(SRC). The photolysis half-life in water is about 15 days(2). |
| Probable Routes of Human Exposure | Occupational exposure to fenazaquin may occur through inhalation and dermal contact with this compound at workplaces where fenazaquin is produced or used. (SRC) |
| Environmental Fate/Exposure Summary | Fenazaquin's production may result in its release to the environment through various waste streamsits use as an acaricide will result in its direct release to the environment. If released to air, a vapor pressure of 2.55X10-8 mm Hg at 25 °C indicates fenazaquin will exist solely in the particulate phase in the atmosphere. Particulate-phase fenazaquin will be removed from the atmosphere by wet or dry deposition. Fenazaquin contains chromophores that absorb at wavelengths >290 nm, and therefore may be susceptible to direct photolysis by sunlight. If released to soil, fenazaquin is expected to have no mobility based upon a Koc range of 18700 to 42100. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 1.0X10-7 atm-cu m/mole. Fenazaquin may not volatilize from dry soil surfaces based upon its vapor pressure. The half-life in soil is approximately 45 days. If released into water, fenazaquin is expected to adsorb to suspended solids and sediment based upon the Koc. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant. A BCF of 500 suggests that bioconcentration in aquatic organisms is high, provided the compound is not metabolized by the organism. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. The photolysis half-life in water is about 15 days. Occupational exposure to fenazaquin may occur through inhalation and dermal contact with this compound at workplaces where fenazaquin is produced or used. (SRC) |
| Antidote and Emergency Treatment | /SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Poisons A and B//SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poisons A and B//SRP:/ Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Consider administering a beta agonist such as albuterol for severe bronchospasm ... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poisons A and B/ |
| Personal protective equipment (PPE) | dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
| Water hazard class (WGK) | 3 |
| RTECS number | VA1382000 |
| UN transport number | UN 2811 6.1/PG 3 |
| Toxicity | LD50 orally in rats, mice (mg/kg): 134, 1480dermally in rabbits (mg/kg): >5000LC50 (96 hr) in bluegill, trout (mg/l): 34.1, 3.8 (Longhurst) |
| Risk statements (R) | 20-25-50/53 |
| Signal word | Danger |
| GHS pictogram | GHS06,GHS09 |
| Hazard symbols | T,N |
| Safety statements (S) | 37-45-60-61 |
| Storage class | 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects |
| GHS hazard statements | H301-H332-H410 |
| REACH registrations | Inactive |
| Hazard class | Acute Tox. 3 OralAcute Tox. 4 InhalationAquatic Acute 1Aquatic Chronic 1 |
| GHS precautionary statements | P261-P264-P270-P273-P301+P310-P304+P340+P312 |
| Hazardous substances data | 120928-09-8(Hazardous Substances Data) |
Applications & Uses
Description
Fenazaquin is a quinazoline acaricide. It has a low aqueous solubility but is highly soluble in many organic solvents. It is not volatile and is not expected to leach to groundwater. It may be persistent in soil and water systems depending on local conditions. Its toxicity to terrestrial and aquatic organisms tends to high to moderate. Fenazaquin is moderately toxic to humans via the oral route and, whilst it may be a respiratory tract irritant no chronic effects have been identified.
Uses
Acaricide and insecticide.
Uses
Fenazaquin is a non-systemic acaricide/insecticide used widely in controlling mites and other related pests in fruits, vegetables and tea.
Uses
Fenazaquin is an acaricide mainly used for control of mites (Eutetranychus, Panonychus and Tetranychus spp.) on pome and citrus fruits and glasshouse-grown ornamental plants.