HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenmedipham
FENDER · M75 · Gusto · EP-452 · Pistol · sn4075 · Suplex · BEETUP
Identifiers & Physical Properties
| CAS No. | 13684-63-4 |
|---|---|
| Molecular formula | C16H16N2O4 |
| Average molar mass | 300.31 g/mol |
| Monoisotopic mass | 300.11100699 g/mol |
| SMILES | COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1 |
| InChIKey | IDOWTHOLJBTAFI-UHFFFAOYSA-N |
| PubChem CID | 24744 |
| ChEMBL | CHEMBL1079421 |
| ChEBI | CHEBI:81734 |
| EC No. | 237-199-0 |
| DTXSID | DTXSID1024255 |
Chemical & Physical Properties
| XLogP | 3.6 |
|---|---|
| Topological polar surface area | 76.7 |
| Hydrogen bond donors | 2 |
| Hydrogen bond acceptors | 4 |
| Rotatable bonds | 5 |
| Heavy atoms | 22 |
| Formal charge | 0 |
| Complexity | 388 |
| SpringerMaterials Properties | Fusion temperature |
| Pesticides | Pesticide -> EPA IRISHerbicidesActive substance -> EU Pesticides database: ApprovedPesticides -> Herbicides, OtherEnvironmental transformation -> Pesticides (parent, predecessor) |
| LogP (partition coefficient) | 3.59 |
| Odor | ODORLESS |
| Density | 0.25 to 0.3 at 68 °F (NTP, 1992)0.25-0.30 g/cu c at 20 °C1.1782 (rough estimate) |
| Color/Form | Colorless crystals |
| Solubility | less than 1 mg/mL at 70 °F (NTP, 1992)COLORLESS, ODORLESS, CRYSTALLINE SOLIDMP 143-144 °CSOLUBILITY: 1 MG/L WATER AT 20 °C, ACETONE 20%, CYCLOHEXANONE 20%, METHANOL 5% /TECHNICAL MATERIAL 97% PURE/4.7 MG/L WATERABOUT 200 G/KG IN ACETONE, CYCLOHEXANONEABOUT 50 G/KG IN METHANOL20 G/KG IN CHLOROFORM2.5 G/KG IN BENZENEABOUT 500 MG/KG IN HEXENE AT ROOM TEMPDMSO (Slightly), Methanol (Slightly)<0.1 g/100 mL at 21 ºC |
| Corrosivity | Non-corrosive |
| Flash point | 74 °C CC100 °C |
| Human Drugs | Pharmaceuticals |
| Endocrine Disruptors | Potential endocrine disrupting compound |
| Melting point | 289 to 291 °F (NTP, 1992)139-142 (143-144 °C)140-144°C |
| Boiling point | 441.54°C (rough estimate) |
| Refractive index | 1.6240 (estimate) |
| Storage conditions | Sealed in dry,Room Temperature |
| pKa (acidity coefficient) | 13.03±0.70(Predicted) |
| Physical state | Solid |
| Color | White to off-white |
| BRN | 2395027 |
| Henry's law constant | 1.2×107 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) |
| Major applications | agricultureenvironmental |
| InChI | 1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20) |
| InChIKey | IDOWTHOLJBTAFI-UHFFFAOYSA-N |
| SMILES | COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1 |
| LogP (partition coefficient) | 3.590 |
| CAS DataBase Reference | 13684-63-4(CAS DataBase Reference) |
| EWG's Food Scores | 4 |
| FDA UNII | UJE31KXP78 |
| NIST Chemistry Reference | Methyl 3-m-tolylcarbamoyloxyphenylcarbamate(13684-63-4) |
| EPA Substance Registry System | Phenmedipham (13684-63-4) |
| UNSPSC Code | 41116107 |
| NACRES | NA.24 |
| GHS pictogram | GHS09 |
| Signal word | Warning |
| GHS hazard statements | H410 |
| GHS precautionary statements | P273-P391-P501 |
| Personal protective equipment (PPE) | Eyeshields, Faceshields, Gloves |
| Hazard symbols | N |
| Risk statements (R) | 50/53 |
| Safety statements (S) | 60-61 |
| UN transport number | UN 3077 |
| Water hazard class (WGK) | 2 |
| RTECS number | FD9050000 |
| Storage class | 11 - Combustible Solids |
| Hazard class | Aquatic Acute 1Aquatic Chronic 1 |
| Hazardous substances data | 13684-63-4(Hazardous Substances Data) |
| Toxicity | (96-hour) for bluegill sunfish 3.98 mg/L, rainbow trout 1.4–3.0 mg/L, Daphnia magna 3.2 mg/L (Worthing and Hance, 1991), harlequin fish 16.5 mg/L (Hartley and Kidd, 1987)acute oral LD50 of pure phenmedipham and the formulated product for rats 3,700 and 10,300 mg/kg, respectively (Ashton and Monaco, 1991). |
Safety & Regulations
| GHS classification | WarningH400: Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]P273, P391, and P501 (click each P-code to see the statement)H400 (99.7%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard] |
|---|---|
| Regulatory information | Regulation (EC) No 396/2005 (amended)Phenmedipham is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)04/58/EC, Reg. (EU) 2017/841, Reg. (EU) 2018/917, Reg. (EU) 2019/707, Reg. (EU) 2020/869, Reg. (EU) 2021/745, Reg. (EU) 2022/708, Reg. (EU) 2023/918, Reg. (EU) 2025/99, Reg. (EU) 2026/1826, Reg. (EU) No 540/2011Phenmedipham: Does not have an individual approval but may be used under an appropriate group standard |
| Other safety information | IMAP assessments - Carbamic acid, (3-methylphenyl)-, 3-[(methoxycarbonyl)amino]phenyl ester: Environment tier I assessment |
| Fire hazards | Flash point data for this chemical are not available, however it is probably combustible. (NTP, 1992) |
| Health hazards | SYMPTOMS: Symptoms of exposure to this compound include photodermatitis, hypoactivity, salivation, muscle weakness, nasal discharge, and labored breathing. |
| Hazards summary | Allergic and photoallergic contact dermatitis reported in farmers[Kanerva, p. 783] Emergency treatment: Carbamate herbicides and fungicides[HSDB] The erythrocyte is the primary target of toxicity with hemolytic anemia observed in sub-chronic (rat, mouse, and dog) and chronic (rat) feeding studiesMethemoglobinemia and other hematological changes also seen in some studiesThe severity of hematological effects noted in sub-chronic studies did not progress with time as evidenced in chronic studiesNo developmental toxicity observed at the highest tested dose in rats (1,350 mg/kg/day) or rabbits (1,000 mg/kg/day) by gavage during gestation[EPA REDs] May cause irritationToxic by skin absorption[Aldrich MSDS] |
| Reactive group | Carbamates |
| FIFRA requirements | As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Phenmedipham is found on List A, which contains most food use pesticides and consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA, as amended in 1988. Case No: 0277Pesticide type: HerbicideRegistration Standard Date: 03/30/87Case Status: OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.Active ingredient (AI): PhenmediphamData Call-in (DCI) Date(s): 10/13/95AI Status: The producers of the pesticide has made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.Tolerances are established for residues of the herbicide phenmedipham, methyl m-hydroxycarbanilate m-methylcarbanilate in or on the following raw agricultural commodities: beets, beets (sugar, roots and tops), and spinach. |
| Reactivity Profile | PHENMEDIPHAM is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. This compound is incompatible with alkaline preparations. (NTP, 1992) |
| Air and Water Reactions | Insoluble in water. |
| Hazard Classes and Categories | Aquatic Acute 1 (99.7%)Hazardous to the aquatic environment (acute) - category 1Specific target organ toxicity - Repeated exposure - Category 2 (blood system) |
| Fire fighting | Fires involving this compound can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992) |
| First aid | EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. |
| Nonfire spill response | SMALL SPILLS AND LEAKAGE: If a spill of this chemical occurs, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with acetone and transfer the dampened material to a suitable container. Use absorbent paper dampened with acetone to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with acetone followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. |
| Preventive Measures | DO NOT BREATHE SPRAY MIST. DO NOT EAT, DRINK, OR SMOKE WHILE SPRAYING. |
| Allowable Tolerances | Tolerances are established for residues of the herbicide phenmedipham, methyl m-hydroxycarbanilate m-methylcarbanilate in or on the following raw agricultural commodities: beets, 0.2 ppm (negligible residue (N))beets (sugar, roots and tops), 0.1 ppm (N)and spinach, 0.5 ppm. |
| Personal Protective Equipment (PPE) | RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)Wear goggles to prevent splashing into eyes. |
| Treatment | If the compound has been ingested, rapid gastric lavage should be performed using 5% sodium bicarbonate. For skin contact, the skin should be washed with soap and water. If the compound has entered the eyes, they should be washed with large quantities of isotonic saline or water. In serious cases, atropine and/or pralidoxime should be administered. Anti-cholinergic drugs work to counteract the effects of excess acetylcholine and reactivate AChE. Atropine can be used as an antidote in conjunction with pralidoxime or other pyridinium oximes (such as trimedoxime or obidoxime), though the use of '-oximes' has been found to be of no benefit, or possibly harmful, in at least two meta-analyses. Atropine is a muscarinic antagonist, and thus blocks the action of acetylcholine peripherally. |
| Health effects | Acute exposure to cholinesterase inhibitors can cause a cholinergic crisis characterized by severe nausea/vomiting, salivation, sweating, bradycardia, hypotension, collapse, and convulsions. Increasing muscle weakness is a possibility and may result in death if respiratory muscles are involved. Accumulation of ACh at motor nerves causes overstimulation of nicotinic expression at the neuromuscular junction. When this occurs symptoms such as muscle weakness, fatigue, muscle cramps, fasciculation, and paralysis can be seen. When there is an accumulation of ACh at autonomic ganglia this causes overstimulation of nicotinic expression in the sympathetic system. Symptoms associated with this are hypertension, and hypoglycemia. Overstimulation of nicotinic acetylcholine receptors in the central nervous system, due to accumulation of ACh, results in anxiety, headache, convulsions, ataxia, depression of respiration and circulation, tremor, general weakness, and potentially coma. When there is expression of muscarinic overstimulation due to excess acetylcholine at muscarinic acetylcholine receptors symptoms of visual disturbances, tightness in chest, wheezing due to bronchoconstriction, increased bronchial secretions, increased salivation, lacrimation, sweating, peristalsis, and urination can occur. Chronically high (>10 years) exposure leads to neuropsychological consequences including disturbances in perception and visuo-motor processing. (A15321) |
| Ecotoxicity values | LC50 Harlequin fish 16.5 mg/l/96 hr /Conditions of bioassay not specified/ /emulsifiable preparation/ |
| Environmental fate | In soils, 71-86% of amount determined 1 day after treatment was degraded in 90 days.TERRESTRIAL FATE: Betanal can degrade in soil through microbial degradation and chemical hydrolysis. Biological screening studies have demonstrated that betanal will biodegrade(1-2)in one study, chemical degradation was faster than microbial degradation(2). Betanal is susceptible to alkaline hydrolysis. The following aqueous hydrolysis half-lives have been reported for buffered betanal solutions at 22 °C(3): 70 days at pH 5, 24 hr at pH 7 and 10 min at pH 9(3). The second-order hydrolysis rate constant was experimentally determined to be 106 L/mol-sec at 25 °C(4) which corresponds to half-lives of 7.5 days at pH 6, 18 hr at pH 7 and 1.8 hr at pH 8(4,SRC). Therefore, degradation rates can be expected to increase with increasing pHmicrobial degradation will become more important as the acidity increases(SRC).TERRESTRIAL FATE: The US Dept of Agric's Pesticide Properties Database lists a soil half-life of 30 days for betanal(1). At recommended application rates, the resultant avg persistence is reported to be 25 days(4). In slightly acidic soils of low humus content, half-lives of 28-55 days were observed(2). Using an alkaline soil (pH 8) and C14-labelled betanal, the concn of betanal dropped from 89.6% at time zero to approximately 11% in 32 days(3)methyl hydroxyphenylcarbamate was the major metabolite with small amounts of m-aminophenol(3). Betanal is reported to remain in the top layers of soil (0 to 2 inches) after herbicidal applications(4) and its Koc value of 2400(1) would suggest a low potential to leach(SRC).AQUATIC FATE: Betanal can degrade in water through microbial degradation and chemical hydrolysis. Biological screening studies have demonstrated that betanal will biodegrade(1-2). Betanal is susceptible to alkaline hydrolysis. The following aqueous hydrolysis half-lives have been reported for buffered betanal solutions at 22 °C(3): 70 days at pH 5, 24 hr at pH 7 and 10 min at pH 9(3). The second-order alkaline hydrolysis rate constant was experimentally determined to be 106 L/mol-sec at 25 °C(4) which corresponds to half-lives of 7.5 days at pH 6, 18 hr at pH 7 and 1.8 hr at pH 8(4,SRC). Therefore, degradation rates in water may increase with increasing pHmicrobial degradation may become more important as the acidity increases(SRC). Based upon a Koc value of 2400(5), some partitioning from the water column to sediment and suspended material may occur(SRC). Aquatic volatilization is not expected to be important fate process(SRC).For more Environmental Fate (Complete) data for BETANAL (9 total), please visit the HSDB record page. |
| Adverse effects | Methemoglobinemia - The presence of increased methemoglobin in the bloodthe compound is classified as secondary toxic effect |
| Exposure routes | Inhalation (L793)oral (L793)dermal (L793) |
| Toxicity summary | Phenmedipham is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active sites of the enzymes. This inhibition is reversible. A cholinesterase inhibitor suppresses the action of acetylcholine esterase. Because of its essential function, chemicals that interfere with the action of acetylcholine esterase are potent neurotoxins, causing excessive salivation and eye-watering in low doses. Headache, salivation, nausea, vomiting, abdominal pain and diarrhea are often prominent at higher levels of exposure. Acetylcholine esterase breaks down the neurotransmitter acetylcholine, which is released at nerve and muscle junctions, in order to allow the muscle or organ to relax. The result of acetylcholine esterase inhibition is that acetylcholine builds up and continues to act so that any nerve impulses are continually transmitted and muscle contractions do not stop. |
| Signs and Symptoms | As with organophosphates, the signs and symptoms are based on excessive cholinergic stimulation. Unlike organophosphate poisoning, carbamate poisonings tend to be of shorter duration because the inhibition of nervous tissue acetylcholinesterase is reversible, and carbamates are more rapidly metabolized. Muscle weakness, dizziness, sweating and slight body discomfort are commonly reported early symptoms. Headache, salivation, nausea, vomiting, abdominal pain and diarrhea are often prominent at higher levels of exposure. Contraction of the pupils with blurred vision, incoordination, muscle twitching and slurred speech have been reported. (L795) |
| EPA IRIS Information | Phenmedipham2.5 x 10 ^-1 mg/kg-day |
| Soil Adsorption/Mobility | Molecular modelling techniques used to estimate the mobility of organic chemicals in soils were evaluated. The effect of molecular structure & water solubility on mobility is discussed.Using several different soils, an Rf value of 0.17 was measured via soil thin-layer chromatography which is indicative of low soil mobility(1). Based upon a water solubility of 4.7 mg/L at 25 °C(2), the Koc of betanal can be estimated to be about 1860 from a regression derived equation(3,SRC). The US Dept Agric's Pesticide Properties Database lists a Koc value of 2400 for betanal(2). According to a suggested classification scheme(4), these Koc values suggest that betanal has low mobility in soil(SRC). Betanal is reported to remain in the top layers of soil (0 to 2 inches) after herbicidal application(5). In a field study in sugar beet soil, applications of betanal remained in the upper 10 cm of soil 2 months after application(6). |
| Human Toxicity Excerpts | Two farmers came separately to the same department of dermatology for diagnosis. One had used phenmedipham for 8 or 9 yr without recognized difficulty in spite of a long history of photodermatitis. However, what was considered an exacerbation of photodermatitis began only a few days after he used phenmedipham in 1978, and a patch test required 14 days to subside. The second farmer presented with a severe, spreading, bullous dermatitis of both hands a few days after he used the compound. He too had used it for 8 or 9 yr without difficulty, but a patch test was positive. |
| Artificial Pollution Sources | Betanal's use as a post-emergence herbicide(1-2) releases the compound directly to the environment through applications in sprays, concentrates and other routes of application(SRC). |
| Personal protective equipment (PPE) | Eyeshields, Faceshields, Gloves |
| Water hazard class (WGK) | 2 |
| RTECS number | FD9050000 |
| UN transport number | UN 3077 |
| Toxicity | (96-hour) for bluegill sunfish 3.98 mg/L, rainbow trout 1.4–3.0 mg/L, Daphnia magna 3.2 mg/L (Worthing and Hance, 1991), harlequin fish 16.5 mg/L (Hartley and Kidd, 1987)acute oral LD50 of pure phenmedipham and the formulated product for rats 3,700 and 10,300 mg/kg, respectively (Ashton and Monaco, 1991). |
| Risk statements (R) | 50/53 |
| Signal word | Warning |
| GHS pictogram | GHS09 |
| Hazard symbols | N |
| Safety statements (S) | 60-61 |
| Storage class | 11 - Combustible Solids |
| GHS hazard statements | H410 |
| Hazard class | Aquatic Acute 1Aquatic Chronic 1 |
| GHS precautionary statements | P273-P391-P501 |
| Hazardous substances data | 13684-63-4(Hazardous Substances Data) |
Applications & Uses
Description
Phenmedipham is a carbamate herbicide used for the control of broadleaved weeds. It has a low aqueous solubility, a low volatility and is not generally expected to leach to groundwaters. It is not normally persistent in soil or water systems. It has a low mammalian toxicity but has been associated with the development of some cancers. Phenmedipham is moderately toxic to most aquatic and terrestrial fauna and flora.
Uses
Postemergence herbicide used to control weeds such as chickweed, dogfennel, foxtail, kochia, nightshade and yellow mustard, in strawberries, beet crops and spinach
Uses
Phenmedipham is an carbanilate selective herbicide used post-emergence in beet crops after the emergence of most broad-leaved weeds and before they develop.
Uses
Herbicide.
General Description
Colorless crystals or white powder.