Ametryn (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R22:Gesundheitssch?dlich beim Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R11:Leichtentzündlich.
S-S?tze Betriebsanweisung:
S2:Darf nicht in die H?nde von Kindern gelangen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S60:Dieses Produkt und sein Beh?lter sind als gef?hrlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Beh?lter dicht geschlossen halten.
Chemische Eigenschaften
Ametryn is a colorless powder
Verwenden
Ametryn is a methylthiotriazine based herbicide which inhibits photosynthesis and other enzymatic processes. Ametryn is used to control broadleaf weeds and annual grasses in pineapple, sugarcane and b
ananas.
Definition
ChEBI: A methylthio-1,3,5-triazine that is 2-(methylsulfanyl)-1,3,5-triazine substituted by an ethylamino and an isopropylamino group at positions 4 and 6 respectively.
Vorbereitung Methode
Ametryn is a colorless crystal synthesized by reacting atrazine
with methyl mercaptan in the presence of an equivalent
of NaOH or by reacting 2-mercapto-4-ethylamino-6-isopropylamino-
1,3,5-triazine with a methylating agent in the
presence of NaOH. It is stable in slightly acidic or alkaline
media, but is hydrolyzed to the inactive 6-hydroxy derivative
in strong acidic or basic media.
Allgemeine Beschreibung
Crystals. Melting point 190-192°F (88-89°C). Used as a herbicide.
Reaktivit?t anzeigen
An amine, organosulfide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. 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.
Hazard
Toxic by ingestion.
Health Hazard
Moderately toxic by ingestion; human toxic-ity data not available; a mild irritant to skinand eye.
LD50 oral (rat): 508 mg/kg
LD50 oral (mouse): 965 mg/kg
LD50 skin (rabbit): >5000 mg/kg.
Landwirtschaftliche Anwendung
Herbicide: Ametryn is a herbicide which inhibits photosynthesis and other enzymatic processes. It is used to control
broadleaf weeds and annual grasses in pineapple, sugarcane and bananas. Uses are being supported in the U.S.
only for the following agricultural crops: field corn, popcorn, sugarcane, and pineapple (EPA, 2005). Used in premixes with atrazine, diuron, simazine, and terbutryn. Not
approved for use in the EU.
Handelsname
AMESIP®; AMERTREX®; AMETREX;
AMETRON SC®; AMETRYNE TECHNICAL®;
AMIGAN®; AMULEX; CRISATRINE®;
CRISATRINA®; DORUPLANT®; EVIK®; G-34162®;
GESAPAX®; HERBIPAK®; KRISMAT®; OXON
PRIMATOL Z 80®; SANCOPAX®; TRINATOX-D®
m?gliche Exposition
Ametryn, a triazine and an organosulfide, amine compound A potential danger to those involved in the manufacture, formulation and application of this selective herbicide.
Carcinogenicity
No carcinogenic response was
observed at the highest dose tested in lifetime studies,
2000 ppm, for both rats and mice.
Environmental Fate
Biological. Cook and Hütter (1982) reported that bacterial cultures were capable of
degrading ametryne forming the corresponding hydroxy derivative (hydroxyametryne)
Soil. Although no products were reported, the half-life in soil is 70–120 days (Worthing
and Hance, 1991)
Groundwater. According to the U.S. EPA (1986) ametryn has a high potential to leach
to groundwater
Chemical/Physical. Hydrolyzes to the 6-hydroxy analog, especially in the presence of
Photolytic. The dye-sensitized photodecomposition of ametryn was studied in aqueous,
aerated solutions (Rejto et al., 1983). When an aqueous ametryn solution was irradiated
in sunlight for several hours, 2-(methylthio)-4-(isopropylamino)-6-amino-
Versand/Shipping
UN2763 Triazine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials
Inkompatibilit?ten
Triazines are incompatible with nitric acid. Amines are chemical bases, they neutralize acids to form salts plus water with an exothermic reaction. 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, nitrides, alkali metals, and sulfides.
Waste disposal
In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.
Ametryn (ISO) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
