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Anilazin

Anilazine

HCID 7541
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Grundinformationen

CAS
101-05-3
Standard-SMILES
Clc1nc(Cl)nc(Nc2ccccc2Cl)n1
InChIKey
IMHBYKMAHXWHRP-UHFFFAOYSA-N
Summenformel
C9H5Cl3N4
Durchschnittliche Molmasse
275,5 g/mol
Monoisotopische Masse
273,957979

Überblick

Anilazine appears as white to tan crystals or white powder. Moderately soluble in organic solvents. Insoluble in water. Melting point 159 °C.

Namen und Bezeichner

Bevorzugter Name
Anilazine
IUPAC
4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazin-2-amine
Lokaler Name
Anilazin
Englischer Name
ANILAZINE
Summenformel
C9H5Cl3N4
Molmasse
275.52

Namen und Synonyme

Anilazine101-05-3AnilazinDYRENEZinochlorKemateBortrysanTriasymTriasynTriazinDyrene 50WAniyaline
Weitere Namen anzeigen
B-622DairinDaireneANIAZINE
Direz4,6-Dichloro-N-(2-chlorophenyl)-1,3,5-triazin-2-amineDyrene FlussigTriazine (pesticide)2,4-Dichloro-6-(o-chloroanilino)-s-triazine(o-Chloroanilino)dichlorotriazineNCI-C086841,3,5-Triazin-2-amine, 4,6-dichloro-N-(2-chlorophenyl)-

Datenbank-Bezeichner

CAS
101-05-3
PubChem CID
7541
DTXSID
DTXSID9020089
ChEMBL
CHEMBL464135
ChEBI
CHEBI:82076
UNII
C6E8Y03ZJN
EC Number
202-910-5
Nikkaji
J5.237J

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3
Polarare Oberfläche (TPSA)
50,7 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
4
Frei drehbare Bindungen
2
Schwere Atome
16
Formalladung
0
Komplexität
221

Experimentelle und physikochemische Eigenschaften

SpringerMaterials PropertiesFusion temperature
Pesticides · 4 Einträge

Agrochemicals -> Pesticide active substances

Active substance -> EU Pesticides database: Not approved

Pesticides -> Fungicides

Pesticide (Anilazine) -> USDA PDB

LogP · 2 Einträge

log Kow = 3.88

3.0

Density · 2 Einträge

1.8 at 68 °F (NTP, 1992) - Denser than water; will sink

1.8 @ 20 °C

Color/FormWhite to tan crystals
Solubility · 4 Einträge

less than 1 mg/mL at 70 °F (NTP, 1992)

SOL IN HYDROCARBON & MOST ORG SOLVENTS

5 g/100 ml toluene, 4 g/100 ml xylene, and 10 g/100 ml acetone, each at 30 °C

In water, 8 mg/l @ 20 °C

CorrosivitySlightly corrosive to metals
Human DrugsPharmaceuticals

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Warning

H315: Causes skin irritation [Warning Skin corrosion/irritation]

P264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Danger

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

P264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P305+P354+P338, P317, P321, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 3 Einträge

2002/2076

1,3,5-Triazin-2-amine, 4,6-dichloro-N-(2-chlorophenyl)-: 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.

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(2-chlorophenyl)-: Environment tier I assessment
DOT LabelClass 9
Fire HazardsFlash point data for this chemical are not available; however, it is probably combustible. (NTP, 1992)
Health HazardsSYMPTOMS: Symptoms of exposure to this compound may include irritation of the gastrointestinal tract and the respiratory tract. Severe eye irritation may occur. Prolonged skin contact may cause irritation.
Hazards Summary · 1 Eintrag

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 3 Einträge

IT HAS BEEN SHOWN THAT THROUGH ... /CONJUGATION/ INVOLVING RING CHLORINE, THIS CMPD CAN COMBINE WITH METABOLIC INTERMEDIATES CONTAINING AMINO & SULFHYDRYL GROUPS ...

THE VARIETY HORRIDUM OF CANADA THISTLE WAS NOT AFFECTED. DYRENE & METABOLITES OF DYRENE WHICH WERE PHYTOTOXIC TO VARIETY MITE LEAF DISKS IN BIOASSAY TESTS WERE ISOLATED FROM TREATED VARIETY MITE & HORRIDUM PLANTS, BUT NONE OF THESE CMPD INJURED THE VARIETY HORRIDUM. ONE METABOLITE WAS FOUND ONLY IN THE VARIETY MITE; THE OTHER 5 OCCURRED IN BOTH VARIETIES. THE METABOLITES WERE APPARENTLY FORMED FROM DYRENE BY CONJUGATION REACTIONS.

Metabolites of amilazine can be found in the urine and the feces.The major identified metabolite is the hydroxylation product, 2-(2-chloroanilino)-s-triazinodione, is mosltly present in the urine.

Absorption, Distribution and ExcretionElimination is quick; almost 98% is excreted within 72 hr in the urine & feces.

Verwendung und Herstellung

Uses · 6 Einträge

Used as a non-systemic foliar fungicide for vegetable crops; [HSDB]

No longer registered with the EPA for use in the US; [HSDB]

Farming (Pesticides) [Category: Industry]

For Dyrene (USEPA/OPP Pesticide Code: 080811) there are 0 labels match. /SRP: Not registered for current 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./

... Used in vegetables, potatoes, and ornamentals for control of Alternaria, Fusarium, Plasmopara, Puccinia, and Rhizoctonia spp. /Former use in US/

Non-systemic foliar fungicide with protective action for control of Septoria spp of wheat (main area of use); early and late blights of potatoes and tomatoes; anthracnose in cucurbits; leaf spot diseases in many crops; Helminthosporium spp. in wheat and barley; brown path, dollar spot, snow mould, and other diseases of turf; Notrytis, Colletotrichum, Leptosphaeria, and Pyrenophora spp. on many crops. Also used on vegetables, ornamentals, berry fruit, melons, watermelons, coffee, and tobacco. /Former use in US/

Zugehörige Reaktionen

5
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 179768
HRID 179768als ProduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaktionsgleichung von HRID 252886
HRID 252886als Eduktuspto-grants-2011_01
Reaktionsgleichung von HRID 1565851
HRID 1565851als ProduktTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaktionsgleichung von HRID 2119203
HRID 2119203als Produktuspto-grants-1987_07
Reaktionsgleichung von HRID 2119204
HRID 2119204als Produktuspto-grants-1987_07

Notizen zur Verbindung

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Decomposition · 2 Einträge

DT50 (22 °C) 730 hr (pH 4), 790 hr (pH 7), 22 hr (pH 9)

When heated to decomposition it emits very toxic fumes of /hydrogen chloride & nitrogen oxides/.

Melting Point · 2 Einträge

318 to 320 °F (NTP, 1992)

159-160 °C

Vapor Pressure · 3 Einträge

Negligible (NTP, 1992)

0.00000001 [mmHg]

6.2X10-9 mm Hg @ 20 °C

Physical Description · 2 Einträge

Anilazine appears as white to tan crystals or white powder. Moderately soluble in organic solvents. Insoluble in water. Melting point 159 °C.

White to tan solid; [Merck Index] Colorless solid; [MSDSonline]

Physikochemische Eigenschaften

Schmelzpunkt
159 · 159-160℃
Siedepunkt
425.99 °C · 425.99°C (rough estimate)
Dichte
1.611 · 1.611
Brechungsindex
1.6 · 1.6000 (estimate)
storage temp.
0 · 0-6°C
pka
0.43 · 0.43±0.10(Predicted)
Wasserlöslichkeit
10 mg/L · 10mg/L(temperature not stated)
Merck
13 · 13,659
BRN
223133 · 223133
Henry's Law Constant
3.5 · 3.5×104 mol/(m3Pa) at 25℃, HSDB (2015)
Stabilität
Stable. Incompatible with oils and alkalies. May corrode some types of metal and alloy.
Major Application
agricultureenvironmental
InChI
1S/C9H5Cl3N4/c10-5-3-1-2-4-6(5)13-9-15-7(11)14-8(12)16-9/h1-4H,(H,13,14,15,16)
InChIKey
IMHBYKMAHXWHRP-UHFFFAOYSA-N
SMILES
Clc1nc(Cl)nc(Nc2ccccc2Cl)n1
CAS Datenbank
101 · 101-05-3(CAS DataBase Reference)
EPA chemische Informationen
Anilazine (101-05-3)

A skin and eye irritant; [HSDB] A severe eye irritant; [CAMEO] A skin and eye irritant; [eChemPortal: ESIS] Very toxic to aquatic organisms; Evidence of skin sensitization in guinea pig tests; Positive patch tests were reported in 6 pickers in tomato fields who developed dermatitis; [CPS&Q: IUCLID]

Reactive GroupAmines, Phosphines, and Pyridines
Special ReportsDHEW/NCI; Bioassay of Anilazine for Possible Carcinogenicity (1978) Technical Rpt Series No.104 DHEW Pub No. (NIH) 78-1354
FIFRA Requirements · 1 Eintrag

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. Anilazine 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: 0114; Pesticide type: fungicide; Registration Standard Date: 12/30/83; Case Status: No products containing the pesticide are actively registered ... The case /is characterized/ as "cancelled." Under FIFRA, pesticide producers may voluntarily cancel their registered products. EPA also may cancel pesticide registrations if registrants fail to pay required fees or make/meet certain reregistration commitments, or if EPA reaches findings of unreasonable adverse effects.; Active ingredient (AI): Anilazine; Data Call-in (DCI) Date(s): 09/30/91; AI Status: The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

Reactivity ProfileANILAZINE is incompatible with oils and alkalis. It is slightly corrosive to metals. (NTP, 1992)
Air and Water ReactionsInsoluble in water. Stable in neutral and slightly acidic aqueous media but hydrolyzes on heating with alkali.
Toxic Combustion ProductsPoisonous gases /eg NOx, HCl, CO/ may be produced when heated. /Atrazine/

Sicherheit und Schutzausrüstung

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

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.

Fire Fighting Procedures · 3 Einträge

If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself 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/

Personnel protection: Wear positive pressure self-contained breathing apparatus when fighting fires involving this material. /Triazine pesticide, solid, NOS/

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use "alcohol" foam, dry chemical or carbon dioxide. /Triazine pesticide, liquid, NOS; Triazine pesticide, liquid, toxic, NOS; Triazine pesticide, liquid, toxic, flammable, NOS/

Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION. You should then dampen the solid spill material with 60-70% methanol, then transfer the dampened material to a suitable container. Use absorbent paper dampened with methanol to pick up any remaining material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent-wash contaminated surfaces with 60-70% methanol 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.

Disposal Methods · 1 Eintrag

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Preventive Measures · 5 Einträge

If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. /Triazine pesticide, solid, NOS/

Personnel protection: Avoid breathing dusts, and fumes from burning material. Keep upwind. Avoid bodily contact with the material. ... Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water. ... If contact with the material anticipated, wear appropriate chemical protective clothing. /Triazine pesticide, solid, NOS/

If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Use water spray to knock-down vapors. /Triazine pesticide, liquid, NOS; Triazine pesticide, liquid, toxic, NOS; Triazine pesticide, liquid, toxic, flammable, NOS/

If material not on fire and not involved in fire: Attempt to stop leak if without undue personnel hazard. /Triazine pesticide, liquid, NOS/

For more Preventive Measures (Complete) data for DYRENE (8 total), please visit the HSDB record page.

Isolation and EvacuationExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Personal Protective Equipment (PPE) · 3 Einträge

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)

Personnel protection: Wear appropriate chemical protective gloves, boots and goggles. /Triazine pesticide, solid, NOS/

Personnel protection: Wear positive pressure self-contained breathing apparatus. Wear appropriate chemical protective clothing. /Triazine pesticide, liquid, NOS; Triazine pesticide, liquid, toxic, NOS; Triazine pesticide, liquid, toxic, flammable, NOS/

Toxikologische Informationen

Health EffectsCan cause dermatitis, irritation of eyes and respiratory tract.
Ecotoxicity Values · 5 Einträge

LC50 Gammarus fasciatus (scuds) 0.27 ug/l/96 hr at 15 °C, mature (95% confidence limit 0.21-0.35 ug/l). Static bioassay without aeration, pH 7.2-7.5, water hardness 40-50 mg/l as calcium carbonate and alkalinity of 30-35 mg/l. /Technical material, 95.5%/

LC50 Salmo gairdneri (rainbow trout) 140 ug/l/96 hr at 13 °C, wt 1.5 g (95% confidence limit 122-161 ug/l). Static bioassay without aeration, pH 7.2-7.5, water hardness 40-50 mg/l as calcium carbonate and alkalinity of 30-35 mg/l. /Technical material, 95.5%/

LC50 Ictalurus punctatus (channel catfish) 240 ug/l/96 hr at 18 °C, wt 0.7 g (95% confidence limit 110-550 ug/l). Static bioassay without aeration, pH 7.2-7.5, water hardness 40-50 mg/l as calcium carbonate and alkalinity of 30-35 mg/l. /Technical material, 95.5%/

LC50 Lepomis macrochirus (bluegill) 320 ug/l/96 hr at 18 °C, wt 1.1 g (95% confidence limit 142-735 ug/l). Static bioassay without aeration, pH 7.2-7.5, water hardness 40-50 mg/l as calcium carbonate and alkalinity of 30-35 mg/l. /Technical material, 95.5%/

For more Ecotoxicity Values (Complete) data for DYRENE (7 total), please visit the HSDB record page.

Environmental Fate · 4 Einträge

Terrestrial Fate: Half-life in damp soil about 12 hours.

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 3,000(SRC), determined from a measured log Kow of 3.88(2) and a regression-derived equation(3), indicates that dyrene is expected to have slight mobility in soil(SRC). Furthermore, anilines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(4). Volatilization of dyrene from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 2.8X10-10 atm-cu m/mole(SRC), based upon its vapor pressure, 6.2X10-9 mm Hg(5), and water solubility, 8 mg/l(5). Dyrene is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(5). At 22 °C, the hydrolytic half-life of dyrene is 30 days, 33 days, and 22 hr at pH 4, 7, and 9, respectively(5), suggesting that hydrolysis will be an important fate process in moist soil(SRC). The half-life of dyrene (100 ppm) in moist and air dried Glouchester loam soil when incubated in sealed jars at 26 °C was 0.5 and 2.5 days, respectively(6). This data suggests that biodegradation and hydrolysis occur in soils(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 3,000(SRC), determined from a measured log Kow of 3.88(2) and a regression-derived equation(3), indicates that dyrene 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 2.8X10-10 atm-cu m/mole(SRC), based upon its vapor pressure, 6.2X10-9 mm Hg(4), and water solubility, 8 mg/l(4). According to a classification scheme(5), an estimated BCF of 93(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). Hydrolysis is expected to be an important fate process in water based upon hydrolytic half-lives of 30 days, 33 days, and 22 hr at pH 4, 7, and 9, respectively(4). Field studies conducted in soils suggest that biodegradation will occur(7), but it is not clear if hydrolysis or biodegradation is the most important degradation pathway and this may be similar in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), dyrene, which has a vapor pressure of 6.2X10-9 mm Hg at 20 °C(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase dyrene may be removed from the air by wet and dry deposition(SRC).

Food Survey Values · 1 Eintrag

Dyrene was identified, not quantified in food residues during the FDA's FY78-82 and FY83-86 regulatory monitoring program(1,2). Dyrene was detected in 11 of 6,391 domestic agricultural commodities during surveillance sampling between FY82 and FY86(3). All of the residues were found on celery. During the same time period, dyrene residues were not found in samples of 12,044 imported agricultural commodities(3). State findings of dyrene residues collected in the FOODCONTAM database reveal 7 positive samples out of 13,980 samples in FY88, and 12 positive samples out of 13,085 samples in FY89(4). Of 6,970 produce samples from San Antonio analyzed during 1989 and 1991, 7 contained dyrene(5).

Adverse EffectsSkin Sensitizer - An agent that can induce an allergic reaction in the skin.
Exposure RoutesOral Dermal Intraperitoneal.
Toxicity SummaryAnilazine was found to be mutagenic.
Signs and SymptomsDiarrhea; vomitting
Acute Toxicity LinkChemical: ANILAZINE
Ongoing Test Status · 1 Eintrag

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=101-05-3]

Soil Adsorption/Mobility · 2 Einträge

ADSORPTION OF TRIAZINES THROUGH EXCHANGE PROCESS TO ORGANIC MATTER & CLAY MINERALS IS DEPENDENT ON PH OF SOLN & ACIDITY OF ADSORBENT SURFACE. HYDROGEN BONDING & HYDROPHOBIC BONDING ARE OTHER MECHANISMS BY WHICH SOIL ORGANIC MATTER ADSORBS TRIAZINE HERBICIDES, ESP AT HIGHER PH LEVELS. /TRIAZINES/

The Koc of dyrene is estimated as 3,000(SRC), using a measured log Kow of 3.88(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that dyrene is expected to have slight mobility in soil. Additionally, anilines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(4), suggesting that mobility will be low in soils(SRC).

Human Toxicity Excerpts · 5 Einträge

ANILAZINE WAS AMONG PESTICIDES USED IN 48 HR SKIN PATCH TESTS ON 39 FEMALE AGRICULTURE WORKERS. RESULTS INDICATED THAT ANILAZINE WAS NOT HIGHLY SENSITIZING, IF AT ALL.

Inhalation hazard from aerosols is apparently low. /Atrazine/

CAN CAUSE IRRITATION OF SKIN WITH PROLONGED CONTACT.

Dyrene is listed as one of the most common causes of pesticide-associated skin disease (California, 1977-1981) /from table/

This product /dyrene/ has caused skin irritation in exposed workers.

Regulatorische Informationen

FIFRA Requirements · 1 Eintrag

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. Anilazine 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: 0114; Pesticide type: fungicide; Registration Standard Date: 12/30/83; Case Status: No products containing the pesticide are actively registered ... The case /is characterized/ as "cancelled." Under FIFRA, pesticide producers may voluntarily cancel their registered products. EPA also may cancel pesticide registrations if registrants fail to pay required fees or make/meet certain reregistration commitments, or if EPA reaches findings of unreasonable adverse effects.; Active ingredient (AI): Anilazine; Data Call-in (DCI) Date(s): 09/30/91; AI Status: The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

Sicherheitsdaten

wgk
3
ridadr
UN3077 9/PG 3
RTECS-Nr.
XY7175000
risk_code
36/38-50/53
Toxizität
LD50 orally in rats: >5000 mg/kg, Mobay Technical Information Sheet, Jan. 1979
hazard_code
Xi,N
safety_code
22-60-61
Speicherklasse
11 - Combustible Solids
Giftige Stoffe Daten
101-05-3(Hazardous Substances Data)
Hazard Classifications
Aquatic Acute 1Aquatic Chronic 1Eye Irrit. 2Skin Irrit. 2
ImpuritiesOVER 90 TECHNICAL & COMMERCIAL PESTICIDE FORMULATIONS WERE SCREENED FOR PRESENCE OF N-NITROSO COMPOUNDS. LESS THAN 1 PPM OF ANY N-NITROSO COMPOUND WAS FOUND AS CONTAMINANT IN ALL TRIAZINES TESTED.
U.S. Production · 2 Einträge

(1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS

(1978) PROBABLY GREATER THAN 2.27X10+6 GRAMS

Consumption Patterns · 5 Einträge

FUNGICIDE FOR VEGETABLE CROPS, 99%; FUNGICIDE FOR TURF, LESS THAN 1% (1978)

In order of decreasing use, it was applied to tomatoes, celery, strawberries, potatoes, onions, and green onions in California, Michigan, Oregon, North Carolina, New York, New Mexico, and Ohio.

Annual use in U.S. Agriculture in 1982 was 118,000 pounds.

Annual use in U.S. Agriculture in 1989 was 237,000 pounds.

Annual use on cropland (1989-1991) was 144,260 pounds, ranking 22nd out of 32 fungicides.

Methods of ManufacturingREACTION OF CYANURIC CHLORIDE WITH O-CHLOROANILINE
Formulations/Preparations · 5 Einträge

USEPA/OPP Pesticide Code 080811; Trade Names: Dyrene; Kemate; Direz; Triasym.

95.5% TECHNICAL

50% wettable powders; dusts, granules.

ANILAZIN

For more Formulations/Preparations (Complete) data for DYRENE (16 total), please visit the HSDB record page.

Use Classification · 2 Einträge

Pharmaceuticals

FUNGICIDES

General Manufacturing Information · 3 Einträge

The WHO Recommended Classification of Pesticides by Hazard identifies Dyrene (technical grade) as an active ingredient believed to be obsolete or discontinued for use as a pesticide.

Compatible with most other pesticides.

U.S.: All uses voluntarily cancelled by Miles, Inc.

Anwendungen

VerwendenPesticide used to control fungus diseases in lawns and turf.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

1-Chlor-2-nitrobenzol4-Methoxy-6-methyl-1,3,5-triazin-2-amin2-Chloranilin2,4,6-Trichlor-1,3,5-triazin
Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: A member of the class of triazenes that is dichlorotriazene in which the hydrogen is replaced by an o-chloroanilino group. A fungicide formerly used to control leaf spots and downy mildew, it is no longer approved for use within the European U ion.