| Starlicide | |
|---|---|
|
3-Chloro-4-methylaniline |
|
|
Other names
3-Chloro-4-methylbenzenamine; 2-Chloro-4-aminotoluene; 3-Chloro-p-toluidine; Gull toxicant; DRC-1339; CPTH |
|
| Identifiers | |
| CAS number | 33240-95-8 |
| PubChem | 7255 |
| ChemSpider | 6985 |
| Jmol-3D images | Image 1 |
|
|
|
|
| Properties[1] | |
| Molecular formula | C7H8ClN |
| Molar mass | 141.6 g mol−1 |
| Appearance | Yellow to brown liquid |
| Density | 1.167 g/cm3 |
| Melting point |
24 °C, 297 K, 75 °F |
| Boiling point |
237-238 °C |
| Solubility in water | Soluble in hot water |
| Hazards | |
| Flash point | 100 °C |
| LD50 | 1500 mg/kg (oral, rat) |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Starlicide or gull toxicant is a chemical avicide that is highly toxic to European starlings and gulls, but less toxic to other birds or to mammals such as humans and pets.
Contents |
The name Starlicide originated as a registered trademark of the animal feed manufacturer Ralston-Purina in St. Louis, Missouri.[2] Starlicide is a small molecule in which a central benzene ring is modified by amine, chloro and methyl substituents in a specific pattern. Because special names exist for benzene rings modified with one or two of these functional groups, several synonymous chemical names may be encountered: 3-chloro-4-methylaniline or 3-chloro-4-methylbenzenamine, 2-chloro-4-aminotoluene, or 3-chloro-p-toluidine.[3] Numbered groups (2-chloro, 4-amino) also may be named out of order; the numbers of such groups equal the number of carbon atoms in the benzene ring separating them from the group implied in the special name.
Preparations of this chemical may be named as a hydrochloride (e.g. "3-chloro-p-toluidine hydrochloride", CPTH), indicating that hydrochloric acid has been used to neutralize the molecule to a salt in which the amine group is protonated and a chloride counterion is present; otherwise the free base is indicated. The chemical salt is also known as DRC-1339.
In 1966 it was reported that Starlicide is lethal to starlings with an acute oral LD50 of 3.8 milligrams per kilogram body weight, but less toxic to most other birds. Grain-eating game birds [such as bobwhite quail,[4] pheasants (Phasianus colchicus) and rooks (Corvus frugilegus)[5]] were acknowledged to be more vulnerable. Hawks and mammals were resistant to the poison. Starlings were killed in a slow, "nonviolent" death by uremic poisoning and congestion of major organs.[6] The effect was described as "a grayish white, frost-like material of uric acid overlaying the serosal surfaces of the various organs, accompanied by sterile inflammation and necrosis in the affected and adjacent tissues" akin to avian visceral gout.[5] The site of action is believed to be in the kidney[7]
Uses for CPTH include killing blackbirds on sprouting rice[8] and on corn and soybean fields.[9] For these and other uses the poison is often given with brown rice. Research continues to improve the effectiveness of delivery on brown rice by causing the poison to be retained on the bait longer and resist degradation by sunlight.[10][11] The effect of the poison is believed to be cumulative: for example, the LC50 for starlings was 4.7 ppm over 30 days, but only 1.0 ppm when fed for 90 days.[4]
In 2009, a culling with DRC-1339 received national attention after USDA employees dispensed the poison in Griggstown, New Jersey to kill an estimated 5,000 starlings that plagued feed lots and dairies on local farms. When "it began raining birds" community members became alarmed, unsure whether a toxin or disease was at work. Two property owners in the area reported collecting over 150 birds each from their land.[12][13]
In January 2011, there was another incident in Yankton, South Dakota, causing public alarm. The USDA had poisoned the birds in Nebraska to protect farmers feeds.