Sulfoxaflor

277.27

277.27

DTXSID0074687

White solid|White powder (99.7% purity); off-white powder (95.6% purity)

74.5

0.802

1.34g/cm3

112 deg C (99.7% purity)

167.7 deg C (decomp) (99.7% purity)

173.8ºC

1.519

Solubility in heptane 0.242 mg/L. Solubility (g/L) in xylene 0.743; 1,2-dichloroethane 39.6; methanol 93.1; acetone 2.17; ethyl acetate 95.2; octanol 1.66. (all at 20 deg C)

1.9X10-8 mm Hg at 25 deg C

Sharp

Henry's Law constant = 1.2X10-11 atm-cu m/moleat 25 °C|Henry's Law constant = 6.83X10-7 Pa-cu m/mol at 20 °C, pH 7 /6.7X10-12 atm-cu m/mol/

P264, P270, P273, P301+P312, P330, P391, P501

H302

SRP: 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 quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P301+P312, P330, P391, and P501|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|Aggregated GHS information provided by 91 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Danger|P260, P261, P264, P270, P271, P272, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P307+P311, P311, P312, P314, P321, P322, P330, P332+P313, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405, and P501

IDENTIFICATION AND USE: Sulfoxaflor is a white powder with a sharp odor that is registered for pesticide use in the USA but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses. Sulfoxaflor is the first member of a new class of insecticides, the sulfoximines, and is a highly efficacious activator of the nicotinic acetylcholine receptor (nAChR) in insects. HUMAN EXPOSURE AND TOXICITY: Sulfoxaflor was shown to have no agonism on human fetal or adult muscle nAChRs. The data support the conclusion that the developmental effects of sulfoxaflor in rats are mediated via sustained agonism on the fetal muscle nAChR during late fetal development and are considered not relevant to humans. ANIMAL STUDIES: Toxicity and mechanistic studies in rats, rabbits, dogs and mice indicate that sulfoxaflor is an activator of the mammalian nAChR as well, but to a much lesser degree and in a species-specific manner. The nervous system and liver are the target organ systems of sulfoxaflor and its major metabolites resulted in hepatotoxicity; including liver weight and enzyme changes, hypertrophy, proliferation, and hepatocellular adenocarcinomas in subchronic and chronic studies in rodents. Developmental toxicity, manifested as skeletal abnormalities and neonatal deaths, was observed in rats only. The skeletal abnormalities, including forelimb flexure, bent clavicles, and hindlimb rotation, likely resulted from skeletal muscle contraction due to activation of the skeletal muscle nAChR in utero. Contraction of the diaphragm, also related to skeletal muscle nAChR activation, prevented normal breathing in neonates and resulted in increased mortality in the reproduction studies. Oral studies of mid- and high-dose sulfoxaflor resulted in decreased food consumption and subsequent decreased body weight as well as changes in the male reproductive system. Effects in the male reproductive organs were observed in the carcinogenicity study in rats that included increased testicular and epididymal weights, atrophy of seminiferous tubules, and decreased secretory material in the coagulating glands, prostate, and seminal vesicles. Additionally, there was an increased incidence of interstitial cell (Leydig cell) tumors, considered secondary to loss of normal testicular function. At the highest dose tested, muscle tremors and twitches, convulsions, hindlimb splaying, increased lacrimation and salivation, decreased pupil size and response to touch, gait abnormalities and decreased rectal temperature were observed. Decreased motor activity was also observed in the mid- and high-dose groups. Sulfoxaflor was negative for chromosomal aberrations with and without metabolic activation, and tested negative in Salmonella typhimurium strains TA 1535, TA 100, TA 1537, TA 98, and E. coli: WP2 uvrA in a standard reverse mutation assay.

Investigators made isolated phrenic nerve-hemidiaphragm preparations from newborn rats. System included a muscle strain gauge transducer, a stimulating electrode fixed to the phrenic nerve, and tissue preparation anchored in a vessel which allowed changing of test solutions on demand. It was postulated that sulfoxaflor would be an agonist toward the embryonic nicotinic acetylcholine receptor (nAChR). Initial tests confirmed muscle contraction and reduced twitch response to phrenic nerve stimulation at 100 uM ACh, with return to normal upon solution wash. Ten uM tubocurarine rapidly reduced muscle tension and twitch response. Sulfoxaflor caused muscle contraction similar to ACh: at 100 uM sulfoxaflor there was no evident change on nerve-stimulated muscle twitch, whereas at 1 mM sulfoxaflor the twitch response was reduced to about 34% of normal. Ten uM tubocurarine administered simultaneously with 1 mM sulfoxaflor blocked muscle contraction by about 50%. Pre-incubation with 10 uM tubocurarine essentially eliminated the muscle contraction by 1 mM sulfoxaflor. Prolonged exposure to 1 mM sulfoxaflor (7 min) led to sustained muscle contraction and reduction in twitch response, which was reversible on washing. Tests support the hypothesis that neonatal death could have arisen from diaphragm failure by impairing respiration.

LD50 Rat oral 1000 mg/kg bw|LD50 Rat dermal >5000 mg/kg bw|LC50 Rat inhalation >2.09 mg/L (4 hr, nose-only exposure)

Sulfoxaflor's production may result in its release to the environment through various waste streams; its use as an insecticide(1) will result in its direct release to the environment(SRC).

TERRESTRIAL FATE: Based on a classification scheme(1), reported Koc values of 11 to 83.3(2,3) indicate that sulfoxaflor is expected to have very high to high mobility in soil(SRC). Volatilization of sulfoxaflor from moist soil surfaces is not expected to be an important fate process(SRC) given a Henry's Law constant of 1.2X10-11 atm-cu m/mole(2). Sulfoxaflor is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.9X10-8 mm Hg at 25 °C(2). Aerobic biodegradation half-life of sulfoxaflor was reported as <1 day in soil(2). In 9 of 10 field dissipation studies on bare-ground or crop plots, sulfoxaflor had half-lives of <2 days, in the tenth study (bare ground) the half-life was 8 days(2).|AQUATIC FATE: Based on a classification scheme(1), Koc values of 11 to 83.3(2,3) indicate that sulfoxaflor is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(4) based upon a Henry's Law constant of 1.2X10-11 atm-cu m/mole(2). Sulfoxaflor is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from its log Kow of 0.802(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Based on an aerobic biodegradation half-life of <1 day in soil(2), biodegradation of sulfoxaflor is expected in water(SRC).|ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), sulfoxaflor, which has a vapor pressure of 1.9X10-8 mm Hg at 25 °C(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase sulfoxaflor may be removed from the air by wet and dry deposition(SRC). Sulfoxaflor does not absorb light at wavelengths >290 nm(3) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).

Sulfoxaflor is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(1). Sulfoxaflor does not absorb light at wavelengths >290 nm(2) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).[(1) USEPA/OPPTS; Pesticide Fact Sheet: Sulfoxaflor. (2013) Washington, DC: Environmental Protection Agency, Off Prevent Pest Tox Sub, 2003. Available at, as of June 10, 2015: http://www.epa.gov/pesticides/factsheets/index.htm (2)

An estimated BCF of 3 was calculated in fish for sulfoxaflor(SRC), using a log Kow of 0.802(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Koc values of 11 to 83.3(1,2) have been reported for sulfoxaflor(1). According to a classification scheme(3), this Koc range suggests that sulfoxaflor is expected to have very high to high mobility in soil.|Sulfoxaflor soil adsorption data(1).[Table#8234]

The Henry's Law constant for sulfoxaflor is reported as 1.2X10-11 atm-cu m/mole(1). This Henry's Law constant indicates that sulfoxaflor is expected to be essentially nonvolatile from moist soil and water surfaces(2). Sulfoxaflor is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.9X10-8 mm Hg(1).

When lactating goats were orally dosed with labelled sulfoxaflor at 12.2 ppm in the diet, approximately 4% of the dose appeared in the milk and 3% in the tissues.

Occupational exposure to sulfoxaflor may occur through inhalation and dermal contact with this compound at workplaces where sulfoxaflor is produced or used. (SRC)

Four beagle dogs/sex/group were dosed by gavage at 0, 1, 3, or 6 mg/kg/day for 1 year with Sulfoxaflor, purity 96.6%... Periodic blood and urine collection was done to estimate tissue clearance and excretion patterns of parent sulfoxaflor. NOEL = 3 mg/kg/day, based on food consumption decrements in the first 2-3 weeks on study in both sexes, on increased soft or watery feces in males, and on a modest increase in tan vomitus in both sexes. Plasma concentration of parent sulfoxaflor over time peaked at about 2 hours, with about 40% of peak residues at 24 hours, with no obvious effect of sex on plasma levels. An estimated terminal plasma half-life of sulfoxaflor was about 20 hours for either sex. Typically about 60% to 80% of administered dose was recovered as parent sulfoxaflor in 24-hr urine collections.|When rats were orally dosed with labelled sulfoxaflor, approximately 93% of the dose was eliminated in the urine and faeces as parent sulfoxaflor. The main metabolite in urine was a glucuronide conjugate of sulfoxaflor metabolite X11721061, accounting for approximately 2-4% of the dose. Several other unidentified minor components, each less than 1% of the administered dose, were present in the urine and fecal samples...|/MILK/ When lactating goats were orally dosed with labelled sulfoxaflor at 12.2 ppm in the diet, approximately 4% of the dose appeared in the milk and 3% in the tissues.|Rats were administered sulfoxaflor, purity 95.6%... containing suitable specific activity of C14 ring-labeled sulfoxaflor, purity 97.6%, with over 2% XR-208 ketone byproduct. Groups were (1) a single low (5 mg/kg) gavage dose, (2) a single high (100 mg/kg) gavage dose, (3) daily low doses of 5 mg/kg unlabeled sulfoxaflor, followed on day 15 with 5 mg/kg labeled sulfoxaflor, or (4) a single iv dose of 5 mg/kg. Sacrifice was at 168 hr. Generally label was measured in blood, excreta, and tissues to assess kinetics. Metabolic residues were determined in urine and feces. Tissue residues were very low or below detection levels. About 65-70% of administered dose was excreted in urine within 12 hr of dosing, with continuing rapid clearing. Feces comprised 4-5% of administered dose within 24 hr. Carbon trap results were normally below detection. There was no apparent effect of 14-day pre-treatment with low doses. In all of these cases, about 92% of administered dose was excreted in urine and 5-7% in feces, with no apparent sex difference and no difference due to dose level. Intravenous dosing yielded 97-101% of estimated administered dose in urine, and 6-9% in feces. As with the gavage treatments, residues in blood or internal organs were minimal after 7 days. Tmax estimates in plasma for single gavage treatments were typically 1-2 hr. Plasma elimination first phase t1/2 regardless of dose or route ranged from 4-6 hr, with second elimination phases of about 40 hr duration. Patterns were comparable based on RBC's except that second phase t1/2 ranged from about 50 to 75 hours. Two large adjacent peaks, identified as the two diastereomers of parent sulfoxaflor, comprised the bulk of radioactivity in excreta. The first of these peaks eluting in urine ("Peak F") comprised about 53% of administered dose, compared to about 37% for the second peak ("Peak G"). This ratio often exceeded 2:1 for the smaller amounts of radioactivity in feces. These results suggest that the labeled test article was not a racemic mixture, and further that metabolism of one isomer might be favored over the other. Other than one glucuronide (designated X11721061), no other metabolite exceeded 1% of administered dose. The glucuronide evidently involved cleavage between the sulfur and the methylene carbon of sulfoxaflor prior to conjugation at the cleavage site. None of the lesser peaks was characterized. This conjugate was only quantifiable in urine...|For more Absorption, Distribution and Excretion (Complete) data for Sulfoxaflor (7 total), please visit the HSDB record page.

Residue levels in milk reached a plateau during days 3-4 of the dosing phase, at about 0.2 mg/kg eq. Similar (14)C levels were found in liver, kidney, milk, and muscle; while lower levels were reported in fat tissues. This study demonstrated that X11719474 is not metabolized in goats: no metabolites were identified, and the radioactivity found in all tissues was from X11719474.|When laying hens were orally dosed with labelled sulfoxaflor metabolite X11719474 at 11.8 ppm in the feed, approximately 0.5% of the applied dose was recovered in the combined eggs, fat, and tissues. Similar (14)C levels were noted in liver, muscle, and egg; lower levels were found in fat tissues. Approximately 92% of the dose was recovered from the excreta, and 0.3% in the cage rinse. Residue levels in eggs reached a plateau by day 4 of the dosing phase, with no compounds other than X11719474 being identified. This study demonstrated that X11719474 is not metabolized in hens: no metabolites were identified and the radioactivity found in all tissues was from X11719474. /Sulfoxaflor metabolite/|All metabolites /tested/ were less toxic than the parent compound, except for X11519540, which had higher acute and higher short-term toxicity than the parent.|X11721061, a plant and animal (rat) metabolite of sulfoxaflor, was of low acute oral toxicity in rats (LD50 > 2000 mg/kg bw) and showed no genotoxic potential in vitro in mammalian or microbial test systems. In a 28-day oral toxicity study in rats, the NOAEL was 3000 ppm (equal to 236 mg/kg bw per day), based on reduced feed consumption at 8000 ppm (equal to 622 mg/kg bw per day). /Sulfoxaflor metabolite/

Four beagle dogs/sex/group were dosed by gavage at 0, 1, 3, or 6 mg/kg/day for 1 year with Sulfoxaflor... An estimated terminal plasma half-life of sulfoxaflor was about 20 hours for either sex.|.../In/ F344/DuCrl rats...plasma samples were evaluated to find an elimination t1/2 of 8-9 hours.|Rats were administered sulfoxaflor, purity 95.6%... containing suitable specific activity of C14 ring-labeled sulfoxaflor, purity 97.6%, with over 2% XR-208 ketone byproduct. Groups were (1) a single low (5 mg/kg) gavage dose, (2) a single high (100 mg/kg) gavage dose, (3) daily low doses of 5 mg/kg unlabeled sulfoxaflor, followed on day 15 with 5 mg/kg labeled sulfoxaflor, or (4) a single iv dose of 5 mg/kg. ... Plasma elimination first phase t1/2 regardless of dose or route ranged from 4-6 hr, with second elimination phases of about 40 hr duration. Patterns were comparable based on RBC's except that second phase t1/2 ranged from about 50 to 75 hours. ...

This report effectively applies a mode of action sequence... to explain the non-significantly elevated incidence of preputial gland carcinomas in the rat combined study. The sequence proposed is: (1) increased dopamine release from the hypothalamus, causing (2) reduced prolactin secretion from the pituitary, in turn causing (3) reduced stimulation of prolactin receptors on Leydig cells, which reduces LH receptor density in Leydig cells, causing (4) downregulation of LH receptor gene expression, causing (5) transient decrease in serum testosterone, leading to (6) increased serum LH levels, causing (7) increased serum testosterone via hypothalamic/pituitary/gonadal feedback loop, leading to (8) increased preputial gland carcinomas due to slightly increased higher circulating testosterone. Authors note that item (3) does not appear to relate to humans (which statement is consistent with published literature)...|Sulfoxaflor (X11422208), a novel agricultural molecule, induced fetal effects (forelimb flexure, hindlimb rotation, and bent clavicle) and neonatal death in rats at high doses (= 400 ppm in diet); however, no such effects occurred in rabbit dietary studies despite achieving similar maternal and fetal plasma exposure levels. Mode-of-action (MoA) studies were conducted to test the hypothesis that the effects in rats had a single MoA induced by sulfoxaflor agonism on the fetal rat muscle nicotinic acetylcholine receptor (nAChR). The studies included cross-fostering and critical windows of exposure studies in rats, fetal... and adult... rat and human muscle nAChR in vitro agonism experiments, and neonatal rat phrenic nerve-hemidiaphragm contracture studies. The weight of evidence from these studies supported a novel MoA where sulfoxaflor is an agonist to the fetal, but not adult, rat muscle nAChR and that prolonged agonism on this receptor in fetal/neonatal rats causes sustained striated muscle contracture resulting in concomitant reduction in muscle responsiveness to physiological nerve stimulation. Fetal effects were inducible with as little as 1 day of exposure at the end of gestation, but were rapidly reversible after birth, consistent with a pharmacological MoA. With respect to human relevance, sulfoxaflor was shown to have no agonism on human fetal or adult muscle nAChRs. Taken together, the data support the hypothesis that the developmental effects of sulfoxaflor in rats are mediated via sustained agonism on the fetal muscle nAChR during late fetal development and are considered not relevant to humans.

/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 as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on 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. /Sulfur and related compounds/|/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 necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema 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 ... . Administer activated charcoal ... . Cover skin burns with dry sterile dressings after decontamination ... . /Sulfur and related compounds/|/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 bronchospasms ... . Monitor cardiac rhythm and treat arrhythmias if necessary ... . Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Consider vasopressors if patient is hypotensive with a normal fluid volume. Watch for signs of fluid overload ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Sulfur and related compounds/

/ALTERNATIVE and IN VITRO TESTS/ ... With respect to human relevance, sulfoxaflor was shown to have no agonism on human fetal or adult muscle nAChRs. ...The data support the hypothesis that the developmental effects of sulfoxaflor in rats are mediated via sustained agonism on the fetal muscle nAChR during late fetal development and are considered not relevant to humans.

N-(methyloxido(1-(6-(trifluoromethyl)-3-pyridinyl)ethyl)gamma(4)-sulfanylidene) cyanamide

Closer SC (Dow Agrosciences LLC): Active ingredient: Sulfoxaflor 21.8%.|Transform WG (Dow Agrosciences LLC): Active ingredient: Sulfoxaflor 50.0%.|Sulfoxaflor Technical (Dow Agrosciences LLC): Active ingredient: Sulfoxaflor 97.9%.|GF-2860 Ornamental (Dow Agrosciences LLC): Active ingredient: Sulfoxaflor 20.0%; Spinetoram (amixture of spinetoram-J and spinetoram-L) 20.0%.|For more Formulations/Preparations (Complete) data for Sulfoxaflor (8 total), please visit the HSDB record page.

Analytical Enforcement Methodology: Adequate enforcement methodology is available to enforce the tolerance expression. High performance liquid chromatographic (HPLC) methods with positive-ion electro spray (ESI) tandem mass spectrometry (LC/MS/MS) were developed for data collection and enforcement of sulfoxaflor residues and the two metabolites.

Agrochemicals -> Insecticides