Propazin

Propazine

HCID 4937CAS 139-40-2

Grundinformationen

Standard-SMILES
CC(C)Nc1nc(Cl)nc(NC(C)C)n1
InChIKey
WJNRPILHGGKWCK-UHFFFAOYSA-N
Summenformel
C9H16N5Cl
Durchschnittliche Molmasse
229,71 g/mol
Monoisotopische Masse
229,10942319

Überblick

Propazine can cause developmental toxicity and female reproductive toxicity according to The Environmental Protection Agency (EPA).

Namen und Bezeichner

Bevorzugter Name
Propazine
IUPAC
6-chloro-2-N,4-N-di(propan-2-yl)-1,3,5-triazine-2,4-diamine
Lokaler Name
Propazin
Englischer Name
2,4-Bis(isopropylamino)-6-chloro-1,3,5-triazine
Summenformel
C9H16ClN5
Molmasse
229.71

Namen und Synonyme

propazine139-40-2GesamilProzinexMilogardPlantulinPrimatol PPropazinPropasin2-Chloro-4,6-bis(isopropylamino)-s-triazinePropazine (herbicide)Geigy 30,028
Weitere Namen anzeigen
maxx90MILO-PRO
Caswell No. 1842-Chloro-4,6-bis(isopropylamino)-1,3,5-triazineMaxx 906-Chloro-N,N'-bis(1-methylethyl)-1,3,5-triazine-2,4-diamine2,4-Bis(isopropylamino)-6-chloro-s-triazineG 30028G-300286-Chloro-N,N'-diisopropyl-1,3,5-triazine-2,4-diyldiamine

Datenbank-Bezeichner

CAS
139-40-2、1655498-05-7
PubChem CID
4937
DTXSID
DTXSID3021196
ChEMBL
CHEMBL1333189
ChEBI
CHEBI:38067
UNII
UYP5U99Q5T
EC Number
109-875-4、205-359-9
Nikkaji
J3.630G

Eigenschaften

Berechnete Struktureigenschaften

XLogP
2,9
Polarare Oberfläche (TPSA)
62,7 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
5
Frei drehbare Bindungen
4
Schwere Atome
15

Experimentelle und physikochemische Eigenschaften

pHVery weak base
SpringerMaterials PropertiesBoiling point
Pesticides · 6 Einträge

Pesticide -> EPA IRIS

Herbicides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Herbicides, Triazine

Pesticides -> Herbicides

Pesticide

LogP · 3 Einträge

log Kow = 2.93

2.93

3.09

Density · 2 Einträge

1.162 g/cu cm at 20 °C

1.162 g/cm³

Color/Form · 2 Einträge

Colorless powder

Crystals

Physikochemische Eigenschaften

Schmelzpunkt
212 · 212-214°C
Siedepunkt
368.7 °C · 368.7°C (rough estimate)
Dichte
1.162 · 1.162
Dampfdruck
0 Pa · 0Pa at 25℃
Brechungsindex
1.611 · 1.6110 (estimate)
Flammpunkt
11 °C · 11 °C

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Warning

H351: Suspected of causing cancer [Warning Carcinogenicity]

P203, P273, P280, P318, P391, P405, and P501 (click each P-code to see the statement)

Warning

H351 (100%): Suspected of causing cancer [Warning Carcinogenicity]

P203, P273, P280, P318, P391, P405, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 4 Einträge

Hazard Traits - Developmental Toxicity; Reproductive Toxicity

2002/2076

Status: Active Update: 14-09-2010 https://echa.europa.eu/registration-dossier/-/registered-dossier/10793

Propazine: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - 1,3,5-Triazine-2,4-diamine, 6-chloro-N,N'-bis(1-methylethyl)-: Environment tier I assessment
Fire HazardsCombustible. Gives off irritating or toxic fumes (or gases) in a fire. Heating will cause rise in pressure with risk of bursting.
Fire PotentialNONFLAMMABLE.
Hazards Summary · 2 Einträge

An eye irritant; [ICSC] A mild skin, eye, and upper respiratory tract irritant; [HSDB] For the triazine herbicides, systemic toxicity unlikely unless large amounts are ingested; May cause irritation; [EPA Pesticides, p. 121]

The major hazards encountered in the use and handling of propazine stem from its toxicologic properties. Toxic by all routes (ie, inhalation, ingestion, and dermal contact), exposure to this colorless powder may occur from its maufacture and use as an herbicide. Effects from exposure may include shortness of breath, muscle spasms, ataxia, and anorexia. In activities and situations where over exposure may occur, wear a self-contained breathing apparatus and personal protective clothing. If contact should occur, immediately flush affected skin or eyes with running water for at least 15 minutes. Remove contaminated clothing and shoes at the site. While propazine does not ignite easily, it may burn with the production of irritating and poisonous gases. For fires involving propazine, extinguish with dry chemical, CO2, Halon, water spray, fog, or standard foam. Propazine may be shipped domestically via air, rail, road, and water, in containers bearing the label "Poison". Small dry spills of propazine may be placed into a clean, dry, covered container for later disposal (liquid solutions are first absorbed in sand or other noncombustible absorbent). Large liquid spills should be diked far ahead to prevent propazine from entering water sources and sewers. Before implementing land disposal of propazine, consult with regulatory agencies for guidance.

EC ClassificationSymbol: Xn, N; R: 40-50/53; S: (2)-36/37-60-61

Sicherheit und Schutzausrüstung

Fire FightingUse water spray, foam, powder, carbon dioxide.
First Aid Measures · 4 Einträge

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

Rinse with plenty of water (remove contact lenses if easily possible).

Rinse mouth.

Safe StorageProvision to contain effluent from fire extinguishing. Store in an area without drain or sewer access.
Fire Fighting Procedures · 2 Einträge

This chemical is a combustible liquid. Use dry chemical, carbon dioxide, water spray, or alcohol foam extinguishers. Poisonous gases are produced in fire including nitrogen oxides and chlorine. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position. If employees are expected to fight fires, they must be trained and equipped in OSHA 1910.156.

If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itslef does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use "alcohol foam", dry chemical or carbon dioxide. /Triazine pesticide, solid NOS/

Storage Conditions · 2 Einträge

Do not contaminate water, food or feed by storage or disposal. ... Store product in original container only, away from other pesticides, fertilizer, food for feed. /Propazine 4L/

Store in cool, dry, well-ventilated area out of reach of children and animals.

Cleanup Methods · 1 Eintrag

Evacuate persons not wearing protective equipment from area of spill or leak until clean-up is complete. Remove all ignition sources. Collect powdered material in the most convenient and safe manner and deposit in sealed containers. Ventilate area after clean-up is complete. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Contact your Department of Environmental Protection or your regional office of the federal EPA for specific recommendations. If employees are required to clean-up spills, they must be properly trained and equipped. OSHA 1910.120(q) may be applicable.

Toxikologische Informationen

Ecotoxicity Values · 5 Einträge

LC50 Salmo gairdneri (rainbow trout) 18 mg/L for 96 hr /Technical; Conditions of bioassay not specified/

LC50 Lepomis macrochirus (bluegill sunfish) > 100 mg/L for 96 hr /Technical; Conditions of bioassay not specified/

LC50 /Carassius auratus/ (Goldfish) >32.0 mg/L for 96 hr /Conditions of bioassay not specified/

LC50 /Colinus virginianus/ (Bobwhite quail) oral >10000 ppm (8 day diet) /Technical/

For more Ecotoxicity Values (Complete) data for PROPAZINE (12 total), please visit the HSDB record page.

Environmental Fate · 5 Einträge

TERRESTRIAL FATE: Depending upon the region of the USA, soil treated with propazine may be planted to sorghum, corn, or cotton 12 months following application. Propazine will persist longer under dry & cold conditions or other conditions not conducive to chemical & biological degradation.

TERRESTRIAL FATE: THE LONG SOIL PERSISTENCE OF THESE CMPD DOES ... CREATE THE PROBLEM OF SOIL CARRY OVER, WHICH CAN DAMAGE SUCCEEDING CASH CROPS. THEREFORE EXTREME CAUTION MUST BE TAKEN IN THEIR APPLICATION ON CROPLAND TO AVOID SUCH INJURY TO FOLLOWING CROPS. /TRIAZINES/

TERRESTRIAL FATE: Based on a classification scheme(1), Koc values of 84-500 measured in 4 European soils(2), indicate that propazine is expected to have moderate mobility in soil(SRC). Volatilization of propazine from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.6X10-9 atm-cu m/mole(SRC) based upon its vapor pressure, 1.31X10-7 mm Hg(3), and water solubility, 8.6 mg/L(4). Propazine is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). The half-lives for degradation (purportedly mainly soil-catalyzed hydrolysis) of propazine in Hatzenbuhl soil at pH 4.8 and Neuhofen soil at pH 6.5 are 62 and 127 days, respectively(5). Propazine was 36-64% degraded in a series of aerobic soil beds over a 54 week incubation period and 5.7-75% degraded in a series of anaerobic/aerobic cycled soil beds over a 54 week incubation period(6). The greatest amount of biodegradation occurred in beds that were treated with lime and organic matter(6).

TERRESTRIAL FATE: The field half-life of propazine is reported as 135 days(1). A decrease of the amount of inhibition of Italian ryegrass to below 20% inhibition of growth occurred within 4.5 to 25 weeks and in >60 weeks at application rates of 0.25 and 1-4 pounds/acre, respectively(2). Soil treated with propazine is suitable for the planting of sorghum, corn or cotton as soon as 12 months after application, depending upon the region of the US(3). The persistence of propazine in soil has been reported to be at least 2-3 years based upon reduced soybean yields observed after treatment at 4 pound/acre(4).

For more Environmental Fate (Complete) data for PROPAZINE (6 total), please visit the HSDB record page.

Exposure RoutesThe substance can be absorbed into the body by ingestion.
Milk Concentrations · 2 Einträge

...In a goat metabolism study where [14C]propazine was administered orally to a lactating goat at 9.9 ppm (-20x the estimated dietary burden of 0.5 ppm) in the diet for seven consecutive days, total radioactive residues (TRR) were 0.080- 0.238 ppm in milk... . The parent propazine was not detected in goat milk... . The chlorometabolite G-28273 (DACT) was the principal residue identified in milk (63.4% TRR, 0.141 ppm)... . The metabolite G-30033 was identified in milk (9.4% TRR, 0.021 ppm) but not in tissues. The remaining radioactivity in goat milk and tissues was characterized to be comprised of up to six unknown metabolites. ...Each unknown accounted for <7% TRR in milk... .

Another goat metabolism study was performed using a radiolabeled hydroxymetabolite of propazine as the test substance. TRR were 0.025-0.029 ppm in milk ...The test substance, 2-hydroxypropazine, was the major residue identified in all matrices accounting for ...65.0-69.4% TRR (0.017-0.020 ppm) in milk. The only other metabolite identified was desisopropyl hydroxypropazine, which was detected in minor amounts ...8.2-8.5% TRR (0.002 ppm) in milk.

Toxicity Summary · 1 Eintrag

Propazine is a systemic herbicide that is usually applied to the soil, absorbed through leaves and roots, and acts by inhibiting photosynthesis within the targeted plant. It is used as a selective herbicide to control most annual grasses and broadleaf weeds before the weeds emerge or after removal of weed growth. Propazine is formulated as a flowable concentrate, is registered for use on container-grown ornamentals in greenhouses, and is to be applied through flood or drench nozzles only. ... Propazine has a low order of acute toxicity via the oral (Category IV), dermal (Category IV), and inhalation (Category III) routes of exposure. It is not an eye or skin irritant, or a dermal sensitizer. In a sub-chronic developmental study, incomplete or absent bone formation or ossification was observed in fetal rats following exposure of pregnant rats to propazine. These developmental effects are presumed to occur after a single exposure and are therefore appropriate for consideration in the acute exposure scenario for dietary risk from food. These adverse effects were the basis for identification of a developmental endpoint for acute dietary exposure to propazine in females ages 13 to 49. The corresponding highest dose or level of exposure at which these adverse effects were not observable in female rats ("no observed adverse effects level" or NOAEL) was 10 mg/kg/day. After subchronic and chronic exposure to propazine, a variety of species were shown to exhibit neuroendocrine effects resulting in both reproductive and developmental consequences that are considered relevant to humans. These neuroendocrine effects are biomarkers of a neuroendocrine mechanism of toxicity that is shared by several other structurally-related chlorinated triazines including atrazine, simazine, and three chlorinated degradates - G-28279 (des-isopropyl atrazine or DIA), and G-30033 (des-ethyl atrazine or DEA), and G-28273 (diaminochlorotriazine or DACT) - the latter two which can result from the degradation of propazine. These six compounds disrupt the hypothalamic-pituitary-gonadal (HPG) axis, part of the central nervous system, causing cascading changes to hormone levels and developmental delays. For propazine, a neuroendocrine endpoint was identified for chronic dietary exposure based on adverse effects of estrous cycle alterations and luteinizing hormone (LH) surge suppression observed in a LH surge study on female rats exposed to atrazine. The corresponding NOAEL was 1.8 mg/kg/day. ... Propazine's two chlorinated degradates, DEA and DACT, are considered to have toxicity equal to the parent compound in respect to their common neuroendocrine mechanism of toxicity. Another degradate, hydroxy-propazine, was identified, which is expected to have a different toxicological profile from propazine based on the toxicological data available for an analogous metabolite for atrazine, hydroxy-atrazine. ...

Ecotoxicity Excerpts · 2 Einträge

//BIRDS and MAMMALS/ TOXICOLOGICAL INVESTIGATIONS CONDUCTED WITH BOBWHITE QUAIL, MALLARD DUCKS ... HAVE SHOWN PROPAZINE TO HAVE A VERY LOW TOXICITY TO THESE SPECIES.

/AQUATIC SPECIES/ TOXICOLOGICAL INVESTIGATIONS CONDUCTED WITH ... GOLDFISH, RAINBOW TROUT & BLUEGILL SUNFISH HAVE SHOWN PROPAZINE TO HAVE A VERY LOW TOXICITY TO THESE SPECIES.

Regulatorische Informationen

TSCA Requirements · 2 Einträge

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, exposure, and use to EPA as cited in the preamble in 51 FR 41329.

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Propazine is included on this list.

FIFRA Requirements · 2 Einträge

Tolerances are established for negligible residues (N) of the herbicide propazine (2-chloro-4,6-bis(isopropylamino)-s-triazine in or on the following raw agricultural commodities: [Table#3120]

The Agency has evaluated all existing tolerances for sorghum (forage, grain, stover, and sweet) and has determined that the available data provide adequate support to conclude that there is a reasonable certainty that no harm to the general population, infants, children, or any other population subgroup, will result from these tolerances. This decision does not include an assessment of dietary exposure from drinking water because propazine is not currently registered for use on sorghum in the United States and the only registered use for propazine in the United States (a non-food use on container-grown ornamentals in greenhouses) will not result in exposure from drinking water. There are also no residential uses registered for propazine so aggregate risk estimates are the same as those for dietary exposure from food. Dietary exposure to propazine from food was determined to be essentially zero, or less than 1% of the aPAD and cPAD, and not of concern to the Agency. Therefore, no mitigation measures are necessary at this time for the pesticide propazine.

State Drinking Water Guidelines · 2 Einträge

(ME) MAINE 14 ug/L

(FL) FLORIDA 10 ug/L

Federal Drinking Water GuidelinesEPA 10 ug/L

Sicherheitsdaten

wgk
3
tsca
TSCA listed
ridadr
UN 3077
hs_code
29336990
RTECS-Nr.
XY5300000
risk_code
40-50/53-39/23/24/25-23/24/25-11

Chemie und Industrie

Pharmakologische Informationen

Mechanism of Action · 4 Einträge

... Propazine has been grouped with several structurallyrelated, chlorinated triazines (e.g., atrazine, simazine, and 3 chlorotriazine degradates common to atrazine, simazine and propazine) on the basis of a common mechanism of toxicity for disruption of the hypothalamic-pituitary-gonadal (HPG) axis. As a result of their common mechanism of toxicity, exposure to propazine, like exposure to atrazine, results in reproductive and developmental effects and consequences that are considered relevant to humans. These effects form the basis of the regulatory endpoint selection for both compounds. This mechanism involves a central nervous system (CNS) toxicity, specifically, neurotransmitter and neuropeptide alterations at the level of the hypothalamus, which cause cascading changes to hormone levels, e.g., suppression of the luteinizing hormone surge prior to ovulation resulting in prolonged estrus in adult female rats (demonstrated with atrazine and propazine), and developmental delays, i.e., delayed vaginal opening and preputial separation in developing rats (studied in atrazine and propazine). These neuroendocrine effects are considered the primary toxicological effects of regulatory concern. The NOAEL for endocrine changes is protective of systemic toxicity.

After subchronic and chronic exposure to propazine, a variety of species were shown to exhibit neuroendocrine effects resulting in both reproductive and developmental consequences that are considered relevant to humans. These neuroendocrine effects are biomarkers of a neuroendocrine mechanism of toxicity that is shared by several other structurally-related chlorinated triazines including atrazine, simazine, and three chlorinated degradates - G-28279 (des-isopropyl atrazine or DIA), and G-30033 (des-ethyl atrazine or DEA), and G-28273 (diaminochlorotriazine or DACT) - the latter two which can result from the degradation of propazine. These six compounds disrupt the hypothalamic-pituitary-gonadal (HPG) axis, part of the central nervous system, causing cascading changes to hormone levels and developmental delays. For propazine, a neuroendocrine endpoint was identified for chronic dietary exposure based on adverse effects of estrous cycle alterations and luteinizing hormone (LH) surge suppression observed in a LH surge study on female rats exposed to atrazine. The corresponding NOAEL was 1.8 mg/kg/day. Because the database for propazine's potential neuroendocrine effects is less robust than the atrazine database, particularly for the young, the /EPA/ concluded that atrazine data could be used as bridging data for propazine due to the fact that propazine and atrazine share the neuroendocrine mechanism of toxicity described above, and that these neuroendocrine effects are considered the primary toxicological effects of regulatory concern for chronic exposure.

... Their chief mode of action appears to involve carbohydrate metabolism. The chlorinated s-triazines inhibit starch accumulation by blocking the production of sugars. Similar behavior has been shown for the methoxy & methylthio-s-triazines. It has been reported that the s-triazines affect the tricarboxylic acid cycle with activation of phospho-phenyl pyruvate-carboxylase causing the disappearance of sucrose & glyceric acid with the formation of aspartic & malic acids. /s-Triazines/

Since chlorosis is the first sign of the effect of triazines on plants, interference with carbon dioxide assimilation and sugar formation can be expected. Studies showing that Hill reaction is inhibited confirmed this. /Triazines/

Metabolism/Metabolites · 5 Einträge

In animals, the chief urinary metabolites of atrazine, simazine & propazine were the corresponding N-dealkyl triazines, 2-chloro-4-amino-6-(ethylamino)-s-triazine and 2-chloro-4-amino-6-(isopropylamino)-s-triazine. A third metabolite, 2-chloro-4,6-diamino-s-triazine, was reported in the urine of rats dosed with the 3 parent cmpd. This cmpd was the major metabolite in rats.

After propazine was administered to lactating goats, 16 metabolites were separated by ion exchange chromatography of urine but not identified. Carbon dioxide was obtained from dealkylation & oxidation of the side chain isopropyl moieties.

...In a goat metabolism study where [14C]propazine was administered orally to a lactating goat at 9.9 ppm (-20x the estimated dietary burden of 0.5 ppm) in the diet for seven consecutive days, total radioactive residues (TRR) were 0.080- 0.238 ppm in milk, 1.123 ppm in liver, 1.041 ppm in kidney, 0.209 ppm in muscle, and 0.160 ppm in fat. The parent propazine was not detected in goat milk or tissues. The chlorometabolite G-28273 (DACT) was the principal residue identified in milk (63.4% TRR, 0.141 ppm), fat (50.4% TRR, 0.080 ppm), muscle (26.1% TRR, 0.054 ppm), and liver (2.7% TRR, 0.031 ppm). The metabolite G-30033 was identified in milk (9.4% TRR, 0.021 ppm) but not in tissues. The remaining radioactivity in goat milk and tissues was characterized to be comprised of up to six unknown metabolites. Although each unknown accounted for <7% TRR in milk, several unknowns were present at significant levels in goat tissues. None of these unknown residues cochromatographed with the 17 reference standards including standards of known chloro- and hydroxy-metabolites of triazine herbicides.

Another goat metabolism study was performed using a radiolabeled hydroxymetabolite of propazine as the test substance. TRR were 0.025-0.029 ppm in milk, 0.006 ppm in muscle, 0.001 ppm in fat (renal and omental), 0.110 ppm in kidney, and 0.036 ppm in liver taken/collected from a lactating goat administered orally with [U-14C]2-hydroxypropazine at 10.9 ppm in the diet for three consecutive days. Residue characterization was not conducted in muscle and fat tissues because of low radioactivity (<0.010 ppm). The test substance, 2-hydroxypropazine, was the major residue identified in all matrices accounting for 63.5% TRR (0.069 ppm) in kidney, 77.2% TRR (0.028 ppm) in liver, and 65.0-69.4% TRR (0.017-0.020 ppm) in milk. The only other metabolite identified was desisopropyl hydroxypropazine, which was detected in minor amounts in all matrices: 2.9% TRR (0.003 ppm) in kidney, 3.6% TRR (0.001 ppm) in liver and 8.2-8.5% TRR (0.002 ppm) in milk.

For more Metabolism/Metabolites (Complete) data for PROPAZINE (16 total), please visit the HSDB record page.

MeSH Pharmacological ClassificationPesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.
Absorption, Distribution and Excretion · 5 Einträge

Fate in humans and animals: Propazine is readily absorbed and metabolized in the body. At 72 hours after administration of single oral doses of propazine to rats, 66% of the dose was excreted in the urine and 23% was excreted in the feces. This study also indicated that 77% of the dose was absorbed into the bloodstream from the gastrointestinal tract. At 8 days after the dosing, propazine or its metabolites were detected in the rats' lungs, spleen, heart, kidneys, and brain.

In a metabolism study in rats, propazine was administered as a single gavage dose of 1.0 or 100 mg/kg labeled propazine or as 14-daily doses of unlabeled 1.0 mg/kg propazine followed by a single 1.0 mg/kg labeled dose. Corn oil was the vehicle for all treatments. None of the animals died during the study and overall mass balance for all treatment groups ranged from 97.0 to 105.7%. Absorption of propazine from the gastrointestinal tract was rapid and similar for all study groups and no apparent sex-related differences were found. Based on recoveries from urine/ cage wash and tissues, absorption was 73%. Within 48 hours of treatment, 82-95% of the administered dose was recovered from excreta, predominantly the urine. No specific target organs were identified. Labeled propazine was recovered only in the feces of male and female rats in the single high-dose group and female rats in the low dose group. As presented, it cannot be determined if this represents unabsorbed material or material that underwent enterohepatic circulation. Less than 0.1% of the administered dose was detected as CO2 during a pilot study. Thirteen metabolites were recovered; three of which were identified.

The detection of parent hydroxy derivatives in the course of chlorotriazine degradation by animals has been reported. In rats dosed with (14)C-labeled atrazine, simazine & propazine, only small amt, on the order of a few percent, were observed in urine & feces.

When ring-labeled propazine was administered to rats by stomach tube at rates of 41-56 mg/kg, excretion of radioactive material was most rapid during the first 24 hr and decreased to trace amounts by 72 hr. At this time 65.8% and 23% had been recovered from the urine and feces, respectively. At 4 days, the tissue concentrations of related compounds expressed as propazine varied from 19.8 to 39.3 ppm, the lowest values involving the liver and lung. All of the tissue levels fell slowly, the corresponding range at 8 days being 13.0-30.3 ppm. Concentrations tended to be higher in the eviscerated carcass and especially in the skin.

Absorbed principally through plant roots. ... Following root absorption, it is translocated acropetally in the xylem & accumulates in the apical meristems & leaves of plants.

Verwendung und Herstellung

Uses · 6 Einträge

Used as selective pre-emergence herbicide for sorghum, umbellifers (carrots, celery, parsley etc), and greenhouse ornamentals; [HSDB] Previously registered for use on sorghum; New registration in 1998 is for container-grown ornamentals in greenhouses; [Reference #1]

Farming (Pesticides) [Category: Industry]

For Propazine (USEPA/OPP Pesticide Code: 80808) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

For preemergence weed control in grain sorghum and container grown ornamentals in greenhouses. /Propazine 4L/

Selective post-emergence herbicide

Pre-planting or pre-emergence control of grasses and broad-leaved weeds in sorghum and umbelliferous crops (carrots, chervil, parsley etc).

U.S. Production · 2 Einträge

This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3121]

Consumption Patterns4,015,269 lbs/yr
Methods of Manufacturing · 2 Einträge

Propazine is produced by the reaction between cyanuric chloride and two equivalents of isopropylamine.

PRODUCED BY REACTION OF TRICHLORO-1,3,5-TRIAZINE WITH 2 MOLECULAR PROPORTIONS OF ISOPROPYLAMINE IN PRESENCE OF ACID ACCEPTOR, IT FORMS COLORLESS CRYSTALS ...

Formulations/Preparations · 5 Einträge

PROPAZINE 4L Active Ingredient 43.00% Propazine; PROPAZINE TECHNICAL Active Ingredient 98.00% propazine

Mixtures: (propazine +) metolachlor; chlorpropham; prometryn; propachlor.

'Gesamil 50 & 80 wp', wettable powder (500 or 800 g ai/kg); 90 wdg, water-dispersible granule (900 g/kg); 4l, liquid (480 g/l). Mixtures include: milocep, (propazine + metolachlor (1:2)).

... TECHNICAL PRODUCT IS MORE THAN 95% PURE.

For more Formulations/Preparations (Complete) data for PROPAZINE (6 total), please visit the HSDB record page.

Use ClassificationPesticides -> Herbicides

Anwendungen

Verwenden2,4-Bis(isopropylamino)-6-chloro-1,3,5-triazine is used to control annual grasses and broad-leaved weeds in milo and sweet sorghum.

Vor- und nachgelagerte Produkte

Nachgelagerte Produkte

Anbieter50 Anbieter

阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
湖北威德利化学试剂有限公司181-6332-1995 18062128043 · [email protected]
盐城通铭生物科技有限公司15195160625 · [email protected]

Ergänzende Hinweise

DefinitionGeneric name for a preemergence herbicide containing 80% 2-chloro- 4,6-bis(isopropylamino)-s-triazine.

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