Formetanate hydrochloride is a white oryellowish, crystalline solid or powder with a faint odor.Molecular weight=257.75; Freezing/Melting point 5200 C-202 C (decomposes). Hazard Identification (basedon NFPA-704 M Rating System): Health 3, Flammability 1,Reactivity 0. Highly soluble in water.
Formetanate hydrochloride is a white or
yellowish, crystalline solid or powder with a faint odor.
Formetanate is an insecticide and acaricide with contact and
stomach action. It is used to control spider mites and some insects
(Diptera, Hemiptera and Thysanoptera) on ornamentals, fruit, vegetables
and alfalfa.
White powder with a faint odor. Used as a plant insecticide, acaricide, and miticide.
Hydrolyzed at pH less than 4 [EPA, 1998].
FORMETANATE HYDROCHLORIDE is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.
Extremely toxic to humans. Not absorbed through contact with skin. Inhalation or ingestion may cause poisoning. Inhibits cholinesterase activity so effects are in relation to action on nervous system and can result in death.
FORMETANATE HYDROCHLORIDE may burn but does not ignite readily. Container may explode in heat of fire. Hydrolyzed at pH less than 4
Insecticide, Acaricide: Registered for use in the U.S. Not listed for use in
EU countries. An insecticide used for thrips and true
bug control on fruit crops.
CARZOL®; CARZOL® SP;
DICARZOL®; ENT 27566®; EP-332®; MORTON®
EP332; NOR-AM® EP 332; SCHERING® 36056; SN
36056®
Poison by ingestion and
intraperitoneal routes. Mddly toxic by skin
contact. When heated to decomposition it
emits very toxic fumes of NOx and HCl.
A potential danger to those involved
in the manufacture, formulation, and application of this
plant insecticide, acaricide and miticide.
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.
Formetanate is hydrolysed rapidly in field and laboratory soils under
aerobic and anaerobic conditions. It is metabolised by similar pathways in
plants and animals. It is hydrolytically deaminated to produce a formyl
derivative and subsequently hydrolysed at the carbamate ester to give a
phenolic product. The phenol is deformylated to 3-aminophenol and
acetylated to 3-acetamidophenol. Formetanate and most phase 1 metabolites
are found conjugated. Its metabolism has been reviewed by Cool
and Jankowski (1985), Fukuto (1972) and Kuhr and Dorough (1976).
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling and storage. Store in tightly closed containers in a cool, wellventilated area.
UN2757 Carbamate pesticides, solid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1;
Labels: 6.1-Poisonous materials, Technical Name Required.
Formetanate is hydrolysed rapidly under basic conditions. DT50 values at
pH 5, 7 and 9 (22 °C) are reported to be 65 days, 23 hours and 2 hours,
respectively (PM). The photolysis of formetanate hydrochloride in solutions
of distilled water at pH 3.1 and 7.1 or natural river water was
studied. Samples were irradiated for 4 days by a high pressure Hg
lamp immersed in the solutions. Light of wavelength <286 nm was filtered
out. Analysis of solutions was by TLC, IR and MS. The carbamate moiety
was more stable than the formamidine. Photolysis gave four products,
viz. the formaminophenol (2), the 3-aminophenyl carbamate (3), the
formamino compound (4) and 3-hydroxyphenyl methylcarbamate (5), a product of oxidative deamination of formetanate. Yields increased in the
order given. The proposed pathways of photolysis of formetanate are
given in Scheme 1 (Su and Zabick, 1972). Soil surface photolysis occurs
with a DT50 value of 16 hours (PM).
Carbamates are incompatible with strong
acids and bases, and especially incompatible with strong
reducing agents such as hydrideds and active metals.
Contact with active metals or nitrides form flammable gas eous hydrogen. Incompatible with strongly oxidizing acids,
peroxides, and hydroperoxides.
In accordance with 40CFR
165 recommendations for the disposal of pesticides and
pesticide containers. Must be disposed properly by follow ing package label directions or by contacting your local or
federal environmental control agency, or by contacting
your regional EPA office. Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Generators of waste containing this contaminant
(≥kg/mo) must conform with EPA regulations gov erning storage, transportation, treatment, and waste
disposal.
