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Cyanazine

HCID 30773
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
21725-46-2
Standard SMILES
CCNc1nc(Cl)nc(NC(C)(C)C#N)n1
InChIKey
MZZBPDKVEFVLFF-UHFFFAOYSA-N
Molecular formula
C9H13ClN6
Average molar mass
240.69 g/mol
Monoisotopic mass
240.0890221

Overview

Cyanazine can cause developmental toxicity according to state or federal government labeling requirements.

Names & identifiers

Preferred name
Cyanazine
IUPAC
2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile
English name
Cyanazine
Molecular formula
C9H13ClN6
Molecular weight
240.69

Names & synonyms

CYANAZINE21725-46-2BladexFortrolPayzeCyanazinBladex 80WPBlancholSD 15418WL 19805DTXSID10239902-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile
Show more names
80WPMatchCY-PROGramexFortol
W34C4P18WD2-Chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-s-triazine2-((4-Chloro-6-(ethylamino)-1,3,5-triazin-2-yl)amino)-2-methylpropanenitrileDW34182-((4-Chloro-6-(ethylamino)-s-triazin-2-yl)amino)-2-methylpropionitrileDTXCID803990CHEBI:380692-Chloro-4-(1-cyano-1-methylethylamino)-6-ethylamine-1,3,5-triazine

Database identifiers

CAS
21725-46-2
PubChem CID
30773
DTXSID
DTXSID1023990
ChEMBL
CHEMBL1884229
ChEBI
CHEBI:38069
UNII
W34C4P18WD
EC Number
244-544-9
Nikkaji
J3.465G

Properties

Computed structural properties

XLogP
2.2
Topological polar surface area
86.5 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
6
Rotatable bonds
4
Heavy atoms
16
Formal charge
0
Complexity
272

Experimental & physicochemical properties

Chemical ClassesTeratogens
SpringerMaterials PropertiesBoiling point
Pesticides · 6 items

Pesticides

Pesticide -> EPA IRIS

Herbicides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Herbicides, Triazine

Pesticide

LogP · 3 items

log Kow= 2.22

2.24

2.18

Density · 3 items

1.29 kg/l @ 20 °C

Bulk density of technical material: Fluffed 0.35 g/cc; packed 0.45 g/cc

1.26 g/cm³

Color/FormWhite crystals
Solubility · 3 items

Solubility at 25 °C (g/l) in: benzene, 15; chloroform, 210; ethanol, 45; hexane, 15.

In water, 170 mg/l @ 25 °C

Solubility in water, g/100ml at 25 °C: 0.02

CorrosivityFormulated products are noncorrosive

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P273, P301+P317, P330, P391, and P501 (click each P-code to see the statement)

Danger

H301 (31.7%): Toxic if swallowed [Danger Acute toxicity, oral]

P261, P264, P270, P271, P273, P280, P301+P316, P301+P317, P302+P352, P304+P340, P317, P321, P330, P362+P364, P391, P405, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 4 items

Hazard Traits - Developmental Toxicity

2002/2076

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

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 - Propanenitrile, 2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methyl-: Environment tier I assessment
DOT LabelPoison
Fire Hazards · 2 items

Excerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:

Not combustible. Liquid formulations containing organic solvents may be flammable.

Health HazardsExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Hazards Summary · 1 item

Can be absorbed through skin; Animal tests show that this substance possibly causes malformations in human babies. [ICSC] No effect levels in a 2-year feeding study were 12 mg/kg diet for rats and 25 mg/kg diet for dogs; Eliminated within 4 days in animal experiments; [HSDB] Increased eye abnormalities in pups after pregnant rats exposed to 75 mg/kg/day; [REPROTOX] For the triazine herbicides, systemic toxicity unlikely unless large amounts are ingested; May cause irritation; [EPA Pesticides, p. 121] Cyanazine is a developmental toxin in rodent studies. [ACGIH]

Chemistry & industry

Pharmacology

Mechanism of ActionA photosynthesis inhibitor.
Metabolism/Metabolites · 5 items

The primary pathway for metabolism of cyanazine in rats is N-deethylation to yield an amine. In addition, N-acetylcysteinyl derivatives were found in the urine. Dechlorination resulting in a 2-hydroxy triazine was noted, as well as the cyano group hydrolyzed to an amide and then further to a carboxyl analog. The 2-hydroxy compound was a major metabolite in the feces. The bile contained glutathione conjugates.

Redroot pigweed did not hydroxylate cyanazine but did conjugate this compound. In corn, hydrolysis, N-dealkylation and glutathione /conjugation/ were observed. The hydroxy-acid and dealkylated hydroxy-acid were observed in corn. Presence of the carboxyl group on the isopropylamino side chain suppressed dealkylation of the ethylamino group.

Fall panicum and green foxtail contain water and chloroform soluble metabolites 5 days after foliar (14)C cyanazine application. The nitrile group was hydrolyzed and the triazine two position was hydroxylated.

Cyanazine degradation proceeds initially by hydrolysis of the nitrile group and slower hydrolysis of the 2-chloro group. 2-Hydroxycyanazine is the major metabolite found in rat feces. The rat also produces the 4-amino derivative and the N-acetylcysteinyl derivative and hydrolyzes the cyano group to the corresponding amide and carboxy derivatives.

Organic nitriles are converted into cyanide ions through the action of cytochrome P450 enzymes in the liver. Cyanide is rapidly absorbed and distributed throughout the body. Cyanide is mainly metabolized into thiocyanate by either rhodanese or 3-mercaptopyruvate sulfur transferase. Cyanide metabolites are excreted in the urine. (L96)

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 · 2 items

Cyanazine is rapidly metabolized and eliminated from the body by rats and dogs (within 4 days). Research showed that after the oral administration of (14)C cyanazine the material was absorbed and metabolized rapidly; about 40% of the administered dose was excreted in the urine and 47% in the feces.

Related reactions

1 records
New reaction record
HRID 1973034 reaction equation
HRID 1973034As reactantuspto-grants-1976_12

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Human Drugs
Pharmaceuticals
Endocrine DisruptorsPotential endocrine disrupting compound
DecompositionWhen heated to decomposition, it emits very toxic fumes of /hydrogen chloride, nitrogen oxides and hydrogen cyanide/.
Melting Point · 2 items

167.5-169 °C

168 °C

Physicochemical properties

Melting point
167 °C · 167°C
Boiling point
383.12 °C · 383.12°C (rough estimate)
Density
1.287 · 1.2870 (rough estimate)
refractive index
1.6 · 1.6000 (estimate)
Flash point
100 °C · 100 °C
storage temp.
4 °C · APPROX 4°C
solubility
100 mg/mL · DMSO: 100 mg/mL (415.47 mM)
form
Granular Powder
pka
1.46 · 1.46±0.41(Predicted)
color
Off-white
Water Solubility
0.0171 g/100 · 0.0171 g/100 mL
Merck
13 · 13,2714
BRN
615509 · 615509
Henry's Law Constant
3.3 · 3.3×106 mol/(m3Pa) at 25℃, Mackay et al. (2006)
Major Application
agricultureenvironmental
InChI
1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)
InChIKey
MZZBPDKVEFVLFF-UHFFFAOYSA-N
SMILES
CCNc1nc(Cl)nc(NC(C)(C)C#N)n1
CAS DataBase Reference
21725 · 21725-46-2(CAS DataBase Reference)
EWG's Food Scores
5 · 5
FDA UNII
34 C4P18WD · W34C4P18WD
Proposition 65 List
Cyanazine
NIST Chemistry Reference
Cyanazine(21725-46-2)
EPA Substance Registry System
Cyanazine (21725-46-2)
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
6 · GHS06,GHS09
Signal word
Danger
Hazard statements
301 · H301-H410
Precautionary statements
264 · P264-P270-P273-P301+P310-P391-P405
PPE
95 · dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Codes
Xn;N,N,Xn,T,F
Risk Statements
22 · 22-50/53-39/23/24/25-23/24/25-36-20/21/22-11-52/53
Safety Statements
37 · 37-60-61-45-36/37-36-26-16
RIDADR
2588 · UN 2588/2811
WGK Germany
3 · 3
RTECS
1490000 · UG1490000
HazardClass
6.1 · 6.1(b)
PackingGroup
III
Storage Class
6.1 C · 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Hazard Classifications
3 OralAquatic · Acute Tox. 3 OralAquatic Acute 1Aquatic Chronic 1
Hazardous Substances Data
21725 · 21725-46-2(Hazardous Substances Data)
Toxicity
50 in · LD50 in rats, mice (mg/kg): 182, 380 orally (Chapman)
Reactive GroupAmines, Phosphines, and Pyridines
EC ClassificationSymbol: Xn, N; R: 22-50/53; S: (2)-37-60-61
UN ClassificationUN Hazard Class: 6.1; UN Pack Group: III
FIFRA Requirements · 1 item

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. Cyanazine 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: 0066; Pesticide type: herbicide; Registration Standard Date: 12/31/94; 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): Cyanazine; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) document for the case/AI.

Reactivity ProfileA triazine derivative.
Chemical DangersDecomposes on heating. This produces toxic and corrosive fumes of hydrogen chloride (see ICSC 0163), nitrogen oxides and cyanides.

Safety & protection

Fire Fighting · 2 items

Excerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:

In case of fire in the surroundings, use appropriate extinguishing media.

First Aid Measures · 4 items

Fresh air, rest. Refer for medical attention.

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

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Refer for medical attention .

First AidExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Safe StorageProvision to contain effluent from fire extinguishing. Separated from food and feedstuffs. Cool. Dry.
Storage ConditionsKeep from domestic animals, particularly cattle.
Nonfire Spill ResponseExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Disposal Methods · 1 item

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.

Spillage DisposalDo NOT wash away into sewer. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Preventive Measures · 2 items

Use with adequate ventilation. Avoid eye, skin contact, breathing dust, or contact with water, feed, or food.

SRP: Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area. Ventilation control of the contaminant as close to its point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants.

Isolation and EvacuationExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Eye PreventionWear safety spectacles.
Inhalation RiskEvaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly.

Toxicology

Ecotoxicity Values · 5 items

LC50 Rasbora heteromorpha (Harlequin fish) 10 mg/l/48 hr /Conditions of bioassay not specified/

LC50 Cyprinodon variegatus (Sheepshead minnow) 18 mg/l/48 hr /Conditions of bioassay not specified/

LC50 Gammarus fasciatus 2.0 mg/l/96 hr @ 15 °C, mature. 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 100%/

LC50 Pimephales promelas (Fathead minnow) 16.3 mg/l/96 hr @ 18 °C (95% confidence interval 14.2-18.0 mg/l), wt 0.9 g. 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 100%/

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

Environmental Fate · 3 items

TERRESTRIAL FATE: The half-life of cyanazine determined in field studies ranged from 6-30 days (1). The half-life of cyanazine measured under laboratory conditions range from 3-19 days at 30 and 5 degrees C, respectively (34% moisture content) to greater than 200 days at 20 degrees C and 8% moisture content(1). Based on a classification scheme(2) and measured Koc values of 182-372(3,4), cyanazine is expected to have moderate mobility in soil(SRC). Volatilization of cyanazine from moist soil surfaces is not expected to be an important fate process(SRC) given a Henry's Law constant of 2.57X10-10 atm-cu m/mole(5). Cyanazine is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.38X10-07 mm Hg(6). Photodegradation of cyanazine is not expected to be an important fate process(7).

AQUATIC FATE: Based on a classification scheme(1) and measured Koc values of 182-372(2,3), cyanazine is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon a Henry's Law constant of 2.57X10-10 atm-cu m/mole(4). Volatilization was not an important process in a model ecosystem study(5). According to a classification scheme(6), an estimated BCF of 5(SRC), from its log Kow of 2.22(7), suggests the potential for bioconcentration in aquatic organisms is low. A half-life of 30-40 days was measured for cyanazine in constructed wetlands; the cyanazine metabolites deethylcyanazine and cyanazine amide were detected in the constructed wetlands(8). At 25 °C and pH range 5.5-9, the un-catalyzed aqueous hydrolysis half-life is at least 200 days(9). Laboratory studies have suggested, however, that natural water constituents, such as humic and fulvic acid, may catalyze the chemical hydrolysis(10).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), cyanazine, which has a vapor pressure of 1.38X10-7 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase cyanazine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 41 hours(SRC), calculated from its rate constant of 9.31X10-12 cu cm/molecule-sec at 25 °C(SRC), determined using a structure estimation method(3). Particulate-phase cyanazine may be removed from the air by wet and dry deposition(SRC). Cyanazine has been detected in widespread rainwater monitoring studies(4); degradation rates while associated with rainwater and clouds are unknown(SRC); these monitoring studies suggest that widespread atmospheric dispersal is possible(4).

Adverse Effects · 1 item

Reproductive Toxin - A chemical that is toxic to the reproductive system, including defects in the progeny and injury to male or female reproductive function. Reproductive toxicity includes developmental effects. See Guidelines for Reproductive Toxicity Risk Assessment.

Exposure RoutesThe substance can be absorbed into the body by inhalation, through the skin and by ingestion.
Toxicity Summary · 1 item

Organic nitriles decompose into cyanide ions both in vivo and in vitro. Consequently the primary mechanism of toxicity for organic nitriles is their production of toxic cyanide ions or hydrogen cyanide. Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. Cyanide is also known produce some of its toxic effects by binding to catalase, glutathione peroxidase, methemoglobin, hydroxocobalamin, phosphatase, tyrosinase, ascorbic acid oxidase, xanthine oxidase, succinic dehydrogenase, and Cu/Zn superoxide dismutase. Cyanide binds to the ferric ion of methemoglobin to form inactive cyanmethemoglobin. (L97)

Acute Toxicity LinkChemical: CYANAZINE
Effluent Concentrations · 1 item

In a study of two watersheds in GA, seasonal losses of cyanazine via field runoff have been reported to range from 0.07 to 1.0% of total field application(1). The daily flux of cyanazine to the Mississippi River and 6 of its tributaries from agricultural use was estimated for the period between May 1991 through March 1992; the estimated daily fluxes over the 11 month period were summed to produce the following total estimated discharges over the 11 month period: Minnesota River: 5.9 kg; White River: 1.6 kg; Illinois River: 23 kg; Platte River: 12 kg; Missouri River: 40 kg; Ohio River: 11 kg; Mississippi River at Clinton, IA: 9.1 kg; Mississippi River at Thebes, IL: 99 kg; Mississippi River at Baton Rouge, LA: 130 kg(2).

ICSC Environmental DataThe substance is toxic to aquatic organisms. This substance does enter the environment under normal use. Great care, however, should be taken to avoid any additional release, for example through inappropriate disposal.
EPA IRIS InformationCyanazine
Soil Adsorption/Mobility · 1 item

An experimentally determined Koc of 200 has been reported (soil type not given)(1). A Koc of 182 was measured in a silty soil(2). Using soil TLC, an intermediate mobility was measured in a silty clay loam (Rf of 0.39) and a high mobility was measured in a sandy loam (Rf of 0.74)(3); the avg Koc for these two soils was reported as 372(4). A Koc of 97 was measured for a silt loam soil from a corn field(5); in field studies using this soil (0.70% organic carbon), a max of 0.04% of surface application was lost through subsurface tile drains(5). In field studies, cyanazine did not leach below a 0.20 m depth in a sandy loam soil(6) or below a 0.30 m depth in a silt loam soil(7). However, cyanazine leached through 0.90 m of a soil composed of 29% clay, 49% silt and 22% sand(8). Cyanazine is reversibly adsorbed to soil particles(9); adsorption increases with increased organic matter content, decreasing soil water and decreasing pH(9). The adsorption of cyanazine by microbial biomass has been observed(10). According to a classification scheme(11), the measured Koc values suggest that cyanazine is expected to have moderate to high mobility in soil(SRC).

Artificial Pollution Sources · 1 item

Cyanazine's use as a pesticide for the control of annual grasses and broadleaf weeds(1) is expected to result in its direct release to the environment(SRC). However, in the US, registration is canceled as of January 1, 2000(2). Sale and distribution of existing stock may continue through September 30, 2002, and all use is prohibited after December 31, 2002(2).

Environmental Biodegradation · 2 items

AEROBIC: The half-life of 2.0 ppm of cyanazine in samples of Regina Heavy Clay soil (70% clay, 25% silt and 5% sand) was determined under various laboratory soil moisture and temperature conditions(1). The half-life at 34% soil moisture content varied from 19 to 3 days at temperatures of 5 and 30 degrees C, respectively; at 8% moisture content and 20 degrees C, the half-life was greater than 200 days (1). In field experiments, the half-life of cyanazine, initially applied at approximately 5.5 lbs/acre, was approximately 30 days; after 56 days, less than 10% of the cyanazine remained(1). In the lab and field experiments, the degradation of cyanazine occurred more rapidly than metribuzin and atrazine(1). The degradation of cyanazine was measured under field conditions over a four year period and under different tillage treatments(2). Approximately 8 percent of cyanazine, initially applied at 5.5-8.8 lbs/acre, remained 2 and 4 weeks after application under no-till and conventional tilling conditions, respectively(2). Approximately 19 and 24 percent of cyanazine, initially present at 250 umol/kg, remained after 42 days in a silt loam soil that was amended with ryegrass and cornmeal, respectively; 36 percent of the applied cyanazine remained in unamended soil and soil amended with poultry litter(3). Three metabolites of cyanazine were observed (in decreasing order): hydroxy cyanazine, cyanazine amide and deethyl cyanazine(3). In a cyanazine metabolite study, cyanazine amide and de-isopropylated atrazine were detected as soil degradation products(4); it was proposed that hydrolysis preceded microbial degradation to yield the de-isopropylated atrazine(4). Persistence studies over a 20-week period at varying temperatures (5, 20, 35 and 50 °C) found that cyanazine degraded within 10 weeks at 5 °C and within 5 weeks at the higher temperatures(5); the initial observed half-lives at the higher temperatures were 1.5-2.0 weeks(5); it has been suggested that degradation of cyanazine at -10 °C is not very likely(6). A half-life of 6 days was observed in a cornfield study in Quebec, Canada(7).

AEROBIC: The persistence and fate of cyanazine was studied in a model aquatic ecosystem(1); after 35 days, only 18% of the initial cyanazine remained(1); the following metabolites were identified(1): 60% N-deethylcyanazine, 0.8% cyanazine amide, 0.3% N-deethylcyanazine amide, 1.2% unknown polar metabolites, and 19% unextractable metabolites(1); degradation of the triazine ring to CO2 proceeded slowly(1); cyanazine and its metabolites did not bioconcentrate in the food chain(1). Cyanazine was found to resist microbial degradation in distilled water amended with various inocculum under aerobic and anaerobic conditions in laboratory experiments(2). A half-life of 30-40 days was measured for cyanazine in constructed wetlands; the cyanazine metabolites deethylcyanazine and cyanazine amide were detected in the constructed wetlands(3). The exact degradation mechanism in water has not been determined with certainty, but may be a combination of microbial degradation and catalyzed hydrolysis(SRC).

Regulatory information

FIFRA Requirements · 1 item

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. Cyanazine 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: 0066; Pesticide type: herbicide; Registration Standard Date: 12/31/94; 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): Cyanazine; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) document for the case/AI.

State Drinking Water Guidelines · 5 items

(AZ) ARIZONA 9 ug/l

(FL) FLORIDA 14 ug/l

(ME) MAINE 1.4 ug/l

(MN) MINNESOTA 1 ug/L

(WI) WISCONSIN 1 ug/l

Federal Drinking Water GuidelinesEPA 1 ug/l

Safety data

PPE
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
wgk
3
rtecs
UG1490000
ridadr
UN 2588/2811
Toxicity
LD50 in rats, mice (mg/kg): 182, 380 orally (Chapman)
risk_code
22-50/53-39/23/24/25-23/24/25-36-20/21/22-11-52/53
Signal word
Danger
Symbol(GHS)
GHS06,GHS09
hazard_code
Xn;N,N,Xn,T,F
safety_code
37-60-61-45-36/37-36-26-16
hazard_class
6.1(b)
Storage Class
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
packing_group
III
Hazard statements
H301-H410
Hazard Classifications
Acute Tox. 3 OralAquatic Acute 1Aquatic Chronic 1
Precautionary statements
P264-P270-P273-P301+P310-P391-P405
Hazardous Substances Data
21725-46-2(Hazardous Substances Data)

In rats and dogs, following oral administration, cyanazine is rapidly metabolized and eliminated within approximately 4 days.

Uses & manufacturing

Uses · 6 items

Used as pre- and post-emergence herbicide for control of annual grasses and broadleaf weeds; [HSDB]

Product registrations voluntarily cancelled in 1999; [ACGIH] Banned in the EU for use as pesticide for plant protection and other pesticides including biocides; [eChemPortal: ESIS]

Farming (Pesticides) [Category: Industry]

For Cyanazine (USEPA/OPP Pesticide Code: 100101) 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./

No products containing the pesticide are actively registered ... The case /is characterized/ as "cancelled."

A pre and postemergence herbicide for control of annual grasses and broadleaf weeds.

Consumption PatternsApproximately 23 million pounds of cyanazine were used annually for agricultural purposes in the U.S. between 1987-1989.
Methods of Manufacturing · 2 items

Acetone cyanohydrin + ammonia + cyanuric chloride + ethylamine (amine formation/amine formation/amine formation)

Prepn: Brit pat 1,132,306; W. Schwarze, U.S. pat 3,505,325 (1968 1970 both to Degussa).

Formulations/Preparations · 5 items

USEPA/OPP Pesticide Code 100101; Trade Names: Bladex; Payze; SD 15418; Bladex 80WP; Cyanazine SD 15418; DW 3418; fortol; Fortrol; WL 19805.

Available as a granular product, wettable powder, flowable concentrate, emulsifiable concentrate, and soluble concentrate. Sold in combination with atrazine, alachlor, metolachlor, paraquat, and butylate.

Dry flowable, liquid

Technical grade >95% pure

Suspension concentrate, wettable powder, granule, DF

Use Classification · 3 items

Pharmaceuticals

Herbicides

HERBICIDES

General Manufacturing Information · 2 items

Reported application rates vary, 0.54-4.8 lb/acre depending upon the crop.

U.S.: Registration is canceled as of January 1, 2000. Sale and distribution of existing stock may continue through September 30, 2002, and all use prohibited after December 31, 2002.

Applications · 5 items

DescriptionCyanazine is an off-white to tan crystallinesolid. Molecular weight=240.73; Freezing/Meltingpoint=167-169℃. Hazard Identification (based on NFPA-704 M Rating System): Health 2, Flammability 1,Reactivity 0. Soluble in water. Physical properties may bealtered by carrier solvents used in commercial formulations

UsesSelective pre-emergence herbicide.

UsesSelective pre- and postemergence herbicide to control weeds in crops such as alfalfa, corn, cotton, sorghum, soybeans, and wetland.

UsesHerbicide used for control of annual grasses and broad-leaved weeds in cereals, cotton, maize, onions, peanuts, peas, potatoes, soybeans, sugarcane and wheat fallow

General DescriptionColorless crystals. Non corrosive when dry. Used as a selective systemic herbicide.

Upstream & downstream products

Upstream raw materials

Cyanuric chlorideIsobutyronitrile

Suppliers87 total

郑州阿尔法化工有限公司+86-18530059196 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]
湖北威德利化学试剂有限公司186-02735115 18062128043 · [email protected]
盐城通铭生物科技有限公司15195160625 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
山东利腾生物科技有限公司+86-18663721413 +86-15552573001 · [email protected]
河北枫嘉新材料科技有限公司+86-0311-87836622 +86-18712993135 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
湖北广奥生物科技有限公司027-02702759223056 18162699093 · [email protected]
上海稳同科技有限公司02151600108 13062666369 · [email protected]
北京海岸鸿蒙标准物质技术有限责任公司13240431552 · [email protected]
上海毕楷科技有限公司18516304666 · [email protected]
ZHEJIANG JIUZHOU CHEM CO., LTD+86-0576225566889 +86-13454675544 · [email protected];[email protected];[email protected]
斯百全化学(上海)有限公司021-021-021-67601398-809-809-809 15221380277 · [email protected]
艾科试剂4008-755-333 18080918076 · [email protected]
成都思天德生物科技有限公司028-83243028 19136088901 · [email protected]
深圳振强药物研发有限公司0755-66853366 13670046396 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
上海将来实业股份有限公司400-0066400 13621662912 · [email protected]
天津阿尔塔科技有限公司022-65378550-8551 · [email protected]
成都零六生物科技有限公司400-1166-196 13458535857 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
上海永叶生物科技有限公司86-021-61559134 15921386130 · [email protected]
常州翔龙医药科技有限公司18915873328 18915873328 · [email protected]
湖北宝凌化工科技有限公司13129969326 · [email protected]
普善实业(陕西)有限公司029-81310890 18165209495 · [email protected]
天津阿尔塔科技有限公司022-6537-8550 15522853686 · [email protected]
TargetMol中国(陶术生物)021-021-33632979 15002134094 · [email protected]
BOC Sciences16314854226; +8616314854226 · [email protected]
厦门志信化学有限公司+86-5922680277 +86-13806087780 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
广州和为医药科技有限公司17612033329 17612033329 · [email protected]
热耳科技(上海)有限公司021-64400900 15800436310 · [email protected]
济南泰恒生物科技有限公司17852565707 · [email protected]
湖北万业众诚化学试剂有限责任公司18671296875 · [email protected]
康幸生物科技(上海)有限公司021-61556450 15800904410
上海西陇生化科技有限公司021-52907766-8042
上海源叶生物科技有限公司18916372613 · [email protected]
山东西亚化学有限公司4009903999 13395398332 · [email protected]
河北贞佳新材料有限公司0319-5925599 13315915972 · [email protected]
南京罗迈美生物科技有限公司[email protected]
上海澄绍生物科技有限公司021-61847300 13341622919 · [email protected]
上海新平精细化学品有限公司18221735425 · [email protected]
山东小野化学股份有限公司0539-6362799 20)
上海贤鼎生物科技有限公司021-021-52271985 17721149837 · [email protected]
陕西缔都医药化工有限公司029-81154043 17391733319 · [email protected]
Shaanxi Didu New Materials Co. Ltd+86-86-17392712779 +86-13289823923 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Cyanazine is a chloro-1,3,5-triazine that is 2-chloro-1,3,5-triazine substituted by an ethyl amino and a (2-cyanopropan-2-yl)amino group at positions 6 and 4 respectively. It has a role as a herbicide, an environmental contaminant and a xenobiotic. It is a 1,3,5-triazinylamino nitrile and a chloro-1,3,5-triazine.