ChemicalBook--->CAS DataBase List--->1610-18-0

1610-18-0

1610-18-0 Structure

1610-18-0 Structure
IdentificationBack Directory
[Name]

PROMETON
[CAS]

1610-18-0
[Synonyms]

G31435
Ontrack
PRAMITOL
PROMETON
Gesafram
Gesagram
Prometone
prometrone
pramitol5p
gesafram50
Primatol O
NSC 163048
ProMeton-d3
ontracic800
Gesafram 50
PRAMITOL(R)
Pramitol 5P
PRIMATOL(R)
Primatol 25e
Ontrack-we-2
Ontracic 800
ProMeton-d14
Methoxypropazine
ProMeton Standard
PROMETON, 250MG,NEAT
PROMETON, 100MG, NEAT
Prometon 250mg [1610-18-0]
prometon (bsi,iso,ansi,wssa)
2,6-Diisopropylamino-4-methoxytriazine
PROMETON PESTANAL (2,4-BIS(ISOPRO-PYLAM
2-METHOXY-4,6-BIS(ISOPROPYLAMINO)TRIAZINE
2,4-bis(isopropylamino)-6-methoxy-s-triazin
2,4-Bis(isopropylamino)-6-methoxy-s-triazine
4,6-Bis(isopropylamino)-2-methoxy-s-triazine
2-METHOXY-4,6-BIS(ISOPROPYLAMINO)-S-TRIAZINE
s-Triazine, 2,4-bis(isopropylamino)-6-methoxy-
2,4-BIS(ISOPROPYLAMINO)-6-METHOXY-1,3,5-TRIAZINE
2-methoxy-4,6-bis(isopropylamino)-1,3,5-triazine
n,n’-diisopropyl-6-methoxy-1,3,5-triazine-2,4-diamine
N2,N4-diisopropyl-6-Methoxy-1,3,5-triazine-2,4-diaMine
n,n’-diisopropyl-6-methoxy-1,3,5-triazine-2,4-diyldiamine
N,N'-Diisopropyl-6-methoxy-1,3,5-triazine-2,4-diyldiamine
5-triazine-2,4-diamine,6-methoxy-n,n’-bis(1-methylethyl)-3
6-methoxy-N2,N4-di(propan-2-yl)-1,3,5-triazine-2,4-diamine
isopropyl-[4-(isopropylamino)-6-methoxy-s-triazin-2-yl]amine
6-methoxy-2-N,4-N-di(propan-2-yl)-1,3,5-triazine-2,4-diamine
6-methoxy-n,n’-bis(1-methylethyl)-1,3,5-triazine-2,4-diamine
1,3,5-Triazine-2,4-diamine, 6-methoxy-N,N'-bis(1-methylethyl)-
[EINECS(EC#)]

216-548-0
[Molecular Formula]

C10H19N5O
[MDL Number]

MFCD00047343
[MOL File]

1610-18-0.mol
[Molecular Weight]

225.29
Chemical PropertiesBack Directory
[Appearance]

Colorless crystalline solid or white powder. Odorless.
[Melting point ]

118-121℃
[Boiling point ]

366.8°C (rough estimate)
[density ]

1.1038 (rough estimate)
[refractive index ]

1.7610 (estimate)
[storage temp. ]

0-6°C
[pka]

4.36±0.41(Predicted)
[Water Solubility ]

0.75g/L(21 ºC)
[Merck ]

13,7880
[EPA Substance Registry System]

Prometon (1610-18-0)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36
[RIDADR ]

UN2763
[RTECS ]

XY4200000
[HS Code ]

29336990
[Hazardous Substances Data]

1610-18-0(Hazardous Substances Data)
[Toxicity]

LD50 in mice, rats (mg/kg): 2160, 2980 orally (Gysin, Knüsli, 1960); LC50 (96 hour) in bluegill sunfish, rainbow trout (ppm): >32, 20 (Tweedy, Kahrs)
Hazard InformationBack Directory
[Hazard]

Toxic by ingestion.
[Potential Exposure]

A nonselective pre-emergence and postemergence triazine herbicide. Use around buildings, storage areas, industrial sites, fences, recreational areas, rights-of-way, railroads, pipelines, lumberyards, tank farms, and similar areas. Controls broadleaf weeds and grasses over an extended period of time
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions) if breathing has stopped, and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water or milk and induce vomiting. Do not make an unconscious person vomit.
[Shipping]

UN2763 Triazine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
[Incompatibilities]

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explo- sions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. UV causes decomposition.
[Chemical Properties]

Colorless crystalline solid or white powder. Odorless.
[Waste Disposal]

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed. In accordance with 40CFR165, follow recom- mendations for the disposal of pesticides and pesticide containers. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.
[Uses]

Nonselective herbicide.
[Uses]

Nonselective preemergence and postemergence herbicide used to control most annual and perennial broad-leaved weeds, grasses and brush weeds on noncrop land.
[Definition]

ChEBI: A methoxy-1,3,5-triazine that is 6-methoxy-1,3,5-triazine-2,4-diamine in which the one of the hydrogens of each amino group is substituted by an isopropyl group.
[Agricultural Uses]

Herbicide: A non-selective pre-emergence and post-emergence herbicide. Use around buildings, storage areas, industrial sites, fences, recreational areas, rights-of-way, railroads, pipelines, lumberyards, tank farms, and similar areas. Controls broadleaf weeds and grasses over an extended period of time. Not listed for use in EU countries. Registered for use in the U.S.
[Trade name]

ACME® Prometon; G-31435®; GESAFRAM® 50; GESAFRAM®; GESAGRAM®; GROUND ZERO®; KLEENWALK®; NIX®; NOXALL®; ONTRACK®; PRIMATOL® (prometon); PROMETONE®; WEED-GO®
[Environmental Fate]

Soil. Degrades in soil yielding hydroxy metabolites and dealkylation of the side chains (Hartley and Kidd, 1987).
Photolytic. Pelizzetti et al. (1990) studied the aqueous photocatalytic degradation of prometon and other s-triazines (ppb level) using simulated sunlight (λ >340 nm) and titanium dioxide as a photocatalyst. Prometon rapidly degraded forming cyanuric acid, nitrates, the intermediate tentatively identified as 2,4-diamino-6-hydroxy-N,N′-bis(1-methylethyl)-1,3,5-triazine and other intermediate compounds similar to those found for atrazine. Mineralization of cyanuric acid to carbon dioxide was not observed (Pelizzetti et al., 1990).
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