Methyl Isonicotinate
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Methyl isonicotinate is a toxic compound, which is used as a
semiochemical A semiochemical, from the Greek wiktionary:σημεῖον, σημεῖον (''semeion''), meaning "signal", is a chemical substance or mixture released by an organism that affects the behaviors of other individuals. Semiochemical communication c ...
. Other names for this compound are 4-pyridine carboxylic acid, and isonicotinic acid methyl ester. This compound is slightly toxic to the human body. It has an irritating effect on the eyes, skin, and respiratory tract. Moreover, the compound is used as the active ingredient in several sticky
thrip Thrips (order Thysanoptera) are minute (mostly long or less), slender insects with fringed wings and unique asymmetrical mouthparts. Different thrips species feed mostly on plants by puncturing and sucking up the contents, although a few are ...
traps to monitor and catch thrips in greenhouses.


History

Methyl isonicotinate, a patented 4-pyridyl carbonyl compound, was found to be a useful semiochemical that does not use any type of
pheromone A pheromone () is a secreted or excreted chemical factor that triggers a social response in members of the same species. Pheromones are chemicals capable of acting like hormones outside the body of the secreting individual, to affect the behavio ...
. No specific history was found on the compound, other than that research has been performed to investigate how this chemical can be used for the management of thrip-pests.


Structure and reactivity

Methyl isonicotinate is a 4-pyridyl carbonyl compound consisting of a pyridine ring attached to methyl carboxylate. No data were available for the reactivity of methyl isonicotinate.


Synthesis

In order to synthesize methyl isonicotinate several substances need to react with one another. These compounds are isonicotinic acid, methanol, sulfuric acid, and sodium carbonate.


Available forms

Methyl isonicotinate (C7H7NO2) has many
constitutional isomers In chemistry, a structural isomer (or constitutional isomer in the IUPAC nomenclature) of a compound is another compound whose molecule has the same number of atoms of each element, but with logically distinct bonds between them. The term metam ...
. Examples are
methyl nicotinate In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula . In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many ...
, 2-nitrotoluene, and
salicylamide Salicylamide (''o''-hydroxybenzamide or amide of salicyl) is a non-prescription drug with analgesic and antipyretic properties. Its medicinal uses are similar to those of aspirin. Salicylamide is used in combination with both aspirin and caffe ...
. All have the same molecular formula, but differ in connectivity between the atoms and are therefore different molecules with specific properties.


Mechanism of action

No information on the mechanism of action was found during the data-search. The only effect of this compound which is found is that it influences the movement of thrips, as mentioned later. Moreover, the compound is used on industrial sites as a laboratory chemical, where it aids in the synthesis of other substances.


Efficacy and side effects


Efficacy

Sticky blue and yellow thrip traps are used to monitor pests on crops. Methyl isonicotinate is the active ingredient in for exampl
LUREM-TR
(Koppers biological systems) and is used to detect a pest in an early stage. The addition of methyl isonicotinate to thrip control methods can increase the success of the trap. The compound affects the movement of thrips as walking and take-off behavior increases. More movement leads to more captured thrips on sticky traps. Usage of methyl isonicotinate in traps can increase the catches up to 20 times depending on the species and the conditions. In addition, the increased movement of thrips increases the exposure of the species to
insecticides Insecticides are substances used to kill insects. They include ovicides and larvicides used against insect eggs and larvae, respectively. Insecticides are used in agriculture, medicine, industry and by consumers. Insecticides are claimed t ...
or biopesticides. There are 10 thrip species known to react to methyl isonicotinate:


Adverse effects

Methyl isonicotinate is known for causing skin corrosion. In low concentration, this compound leads to irritation of the skin. An acute symptom is redness of the skin, but the effects of the substance can be delayed. If the skin has been in contact with the substance, the skin should be flushed with running water for at least 20 minutes and the person should see a doctor. In addition, it causes significant damage to the eye. When the eye has been contaminated with this compound, flush the eyes with running water for a minimum of 15 minutes straight away. During this process, the eyelids should be open. After, it is advised that the person should call an emergency medical center. Also, the respiratory tract may be affected when the system comes in contact with large amounts of methyl isonicotinate. Medical attention is needed. After overexposure one might experience nausea, a headache, dizziness, tiredness, or even vomiting. Lastly, methyl isonicotinate is a combustible liquid.


Toxicity

There are different studies performed on the acute toxicity of methyl isonicotinate. The acute toxicity relates to effects that occur after exposure to a substance or mixture. In the studies on acute toxicity of methyl isonicotinate, the effects were observed in vivo in rodents.


Oral toxicity studies in rats

To examine the oral toxicity of methyl isonicotinate, studies were performed to estimate the
LD50 In toxicology, the median lethal dose, LD50 (abbreviation for "lethal dose, 50%"), LC50 (lethal concentration, 50%) or LCt50 is a toxic unit that measures the lethal dose of a toxin, radiation, or pathogen. The value of LD50 for a substance is the ...
. Based on the studies supported by Tsarichenko (1977), U.S. Library of Medicine (2017) and Gestis Substance Database (2017),
Sprague-Dawley A laboratory rat or lab rat is a brown rat of the subspecies '' Rattus norvegicus domestica'' which is bred and kept for scientific research. While less commonly used for research than mice (see laboratory mouse), rats have served as an importa ...
male and female rats were treated with methyl isonicotinate by oral gavage route. According to the estimated LD50 of 3906 mg/kg, methyl isonicotinate is classified as category V on GLP criteria for acute oral toxicity. Category V substances are identified as causing relatively low acute toxicity hazard. However, the substances could present a danger to vulnerable populations. In a treatment with isonicotinate acid, the rats showed clinical signs such as suppression of the general motor activity, an impairment of motor coordination and an assumption of a lateral position. These signs were all observed at a LD50 of 5000 mg/kg.


Dermal toxicity in rabbits

The dermal toxicity was estimated based on a study supported by Cosmetic ingredient review (2005) on methyl isonicotinate. In this study, rabbits were used to estimate the LD50 for the dermal toxicity of methyl isonicotinate. The rabbits were treated with methyl isonicotinate by dermal application. This study resulted in an estimated LD50 of 3828 mg/kg. Conclusively, methyl isonicotinate can be classified as category V for acute dermal toxicity.


Effects on animals

The European Chemical Agency (
ECHA The European Chemicals Agency (ECHA; ) is an agency of the European Union which manages the technical and administrative aspects of the implementation of the European Union regulation called Registration, Evaluation, Authorisation and Restrict ...
) mentions some effects on animals: Short term toxicity to aquatic invertebrates, aquatic algae, cyanobacteria, and micro-organisms. No other effects on animals were found during the data-search. Furthermore, as mentioned before, the compound can serve as a semiochemical in thrips, affecting their movement and therefore increasing the functionality of traps.


References

{{reflist Semiochemicals