| Identification | More | [Name]
Prometryn | [CAS]
7287-19-6 | [Synonyms]
2,4-BIS ISOPROPYLAMINO-6-METHYLTHIO-S-TRIAZINE
2-methylthio-4,6-bis(isopropyl amino)-1,3,5-triazine
2-Methylthio-4,6-bis(isopropylamino)-1,3,5-triazine
AGRISOLUTIONS
AGROGARD
AURORA KA-3878
CAPAROL
CAPAROL(R)
COTTON-PRO
EFMETRYN
G34161
GESAGARD
GESAGARD(R)
'LGC' (1627)
N，N′-Bis(isopropylamino)-6-methylthio-1，3，5-triazine
N,N'-DIISOPROPYL-6-METHYLSULFANYL-[1,3,5]TRIAZINE-2,4-DIAMINE
PRIMATOL Q(R)
PROMETREX
PROMETRYN
PROMETRYNE | [EINECS(EC#)]
230-711-3 | [Molecular Formula]
C10H19N5S | [MDL Number]
MFCD00055396 | [Molecular Weight]
241.36 | [MOL File]
7287-19-6.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xn,N | [Risk Statements ]
R11:Highly Flammable.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36:Irritating to the eyes.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R20:Harmful by inhalation. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S60:This material and/or its container must be disposed of as hazardous waste . | [RIDADR ]
UN 1648 3/PG 2 | [WGK Germany ]
2 | [RTECS ]
XY4390000 | [HS Code ]
29336990 | [Hazardous Substances Data]
7287-19-6(Hazardous Substances Data) | [Toxicity]
LD50 orally in rats: 3.75 g/kg (Geigy); LC50 (96 hour) in bluegill sunfish, rainbow trout (ppm): 10.0, 2.5 (Tweedy, Kahrs) |
| Hazard Information | Back Directory | [General Description]
Colorless crystals. Used as an herbicide. | [Reactivity Profile]
A triazine derivative. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. | [Potential Exposure]
Prometryn, a triazine herbicide, is
used to control several annual grasses and broadleaf weeds
in terrestrial food and feed crops. Among its major applica-
tions are on cotton and celery and is often used on dill and
pigeon peas. | [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]
Triazine pesticides, solid, toxic, n.o.s. require a
shipping label of “poisonous materials.” This material fall
in DOT/UN Hazard Class 6.1. | [Description]
Prometryn can be used in Pre- and
postemergence to Control Annual grasses,
broadleaf weeds. | [Chemical Properties]
Colorless crystalline solid. | [Waste Disposal]
Dissolve or mix the material
with a combustible solvent and burn in a chemical incinera-
tor 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]
Herbicide. | [Uses]
Prometryn is a methylthiotriazine herbicide used for the control of several annual grasses and broadleaf weeds. Prometryn works by inhibiting the electron transport in target broadleaves and grasses. | [Uses]
Selective herbicide used to control many annual grasses and broad-leaved weeds in
cotton, celery and peas. | [Definition]
ChEBI: A diamino-1,3,5-triazine that is N,N'-di(propan-2-yl)-1,3,5-triazine-2,4-diamine substituted by a methylsulfanediyl group at position 6. | [Production Methods]
Prometryne is made either by reacting propazine with methyl
mercaptan in the presence of one equivalent of NaOH or
by reacting 2-mercapto-4,6-bis(isopropylamino)-5-triazine
with a methylating agent in the presence of NaOH.
Prometryne is made either by reacting propazine with methyl
mercaptan in the presence of one equivalent of NaOH or
by reacting 2-mercapto-4,6-bis(isopropylamino)-5-triazine
with a methylating agent in the presence of NaOH. | [Flammability and Explosibility]
Notclassified | [Agricultural Uses]
Herbicide: Prometryn is used to control several annual grasses and broadleaf weeds in terrestrial food and feed crops. Its major uses are on cotton and celery, and is often used on dill and pigeon peas. Not approved for use in EU countries. Registered for use in the U.S. | [Trade name]
A-1114®; CAPAROL®; COTTON PRO®; G 34161®; GESAGARD®; MERCASIN®; MERCAZIN®; MERKAZIN®; POLISIN®; PRIMAPIN®; PRIMATOL-Q®; PROMET®; PROMETREX®; SELECTIN®; SELECTIN-50®; SELEKTIN®; SESAGARD®; SUPREND®; UVON® | [Carcinogenicity]
No carcinogenic activity was
seen in either the rat or the mouse following lifetime feeding
of up to 1500 or 3000 ppm, respectively. | [Environmental Fate]
Soil. In soil and plants, the methylthio group is oxidized. The proposed degradative
pathway is the formation of the corresponding sulfoxide and sulfone derivatives of prometryn followed by oxidation of the latter to forming hydroxypropazine (Kearney and
Kaufman, 1976). Cook and Hütter (1982) reported that bacterial cultures degraded prometryne to form the corresponding hydroxy derivative (hydroxyprometryne). 14C-Prometryn
was incubated in an organic soil for one year. It was observed that 57.4% of the bound
residues were comprised of prometryn (>50%), hydroxypropazine, mono-n-dealkylated prometryn, mono-N-dealkylated hydroxypropazine, a didealkylated compound [2-(methylthio)-4-amino-6-(isopropylamino)-s-triazine] and unidentified methanol soluble products (Khan and Hamilton, 1980; Khan, 1982). Hydroxyprometryn and ammeline were
reported as hydrolysis metabolites in soil (Somasundaram et al., 1991). The reported halflife in soil is 60 days (Jury et al., 1987).
Photolytic. When prometryn in aqueous solution was exposed to UV light for 3 hours,
the herbicide was completely converted to hydroxypropazine. Irradiation of soil suspensions containing prometryn was found to be more resistant to photodecomposition. About
75% of the applied amount was converted to hydroxypropazine after 72 hours of exposure
(Khan, 1982). The UV (λ = 253.7 nm) photolysis of prometryn in water, methanol, ethanol,
n-butanol and benzene, yielded 2-methylthio-4,6-bis(isoprop-ylamino)-s-triazine. At
wavelengths >300 nm, photodegradation was not observed (Pape and Zabik, 1970). Khan
and Gamble (1983) also studied the UV irradiation (λ = 253.7 nm) of prometryn in distilled
water and dissolved humic substances. In distilled water, 2-hydroxy-4,6-bis(isopropylamino)-s-triazine and 4,6-bis(isopropylamino)-s-triazine formed as major products.
In the presence of humic/fulvic acids, 4-amino-6-(isopropylamino)-s-triazine was also
formed (Khan and Gamble, 1983). Pelizzetti et al. (1990) studied the aqueous photocatalytic degradation of prometryn and other s-triazines (ppb level) using simulated sunlight
(λ >340 nm) and titanium dioxide as a photocatalyst. Prometryn rapidly degraded forming
cyanuric acid, nitrates, sulfates, the intermediate tentatively identified as 2,4-diamino-6-
hydroxy-N,N′-bis(1-methyl-ethyl)-1,3,5-triazine and other intermediate compounds similar to those found for atrazine. It was suggested that the appearance of sulfate ions was
due to the attack of the methylthio group at the number two position. Mineralization of
cyanuric acid to carbon dioxide was not observed (Pelizzetti et al., 1990).
Chemical/Physical. Mascolo et al. (1995) studied the reaction of prometryn (100 μM)
with sodium hypochlorite (10 mM) at 25°C and pH 7. Degradation followed the following
pathway: prometryn → 2,4-(N,N′-diisopropyl)diamino-6-methylsulfinyl-1,3,5-triazine →
2,4-(N,N′-diisopropyl)diamino-6-methylsulfonyl-1,3,5-triazine → 2,4-(N,N′-diisopropyl)diamino-6-methanesulfonate ester 1,3,5-triazine → 2,4-(N,N′-diisopropyl)diamino-6-
hydroxy-1,3,5-triazine. | [storage]
4°C, away from moisture and light | [Toxicity evaluation]
Toxicity class II or III,
slightly to moderately
toxic (depending on
formulation) |
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