Starlicide

Starlicide

Names
Preferred IUPAC name 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
3D model (JSmol)	Interactive image
ChemSpider	6985
ECHA InfoCard	100.002.225
PubChem CID	7255
CompTox Dashboard (EPA)	DTXSID0020286
InChI InChI=1S/C7H8ClN/c1-5-2-3-6(9)4-7(5)8/h2-4H,9H2,1H3
SMILES Clc1cc(N)ccc1C
Properties[1]
Chemical formula	C7H8ClN
Molar mass	141.60 g·mol−1
Appearance	Yellow to brown liquid
Density	1.167 g/cm3
Melting point	24 °C (75 °F; 297 K)
Boiling point	237 to 238 °C (459 to 460 °F; 510 to 511 K)
Solubility in water	Soluble in hot water
Hazards
Flash point	100 °C (212 °F; 373 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose)	1500 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Starlicide or gull toxicant is a chemical avicide that is highly toxic to European starlings (thus the name) and gulls, but less toxic to other birds or to mammals such as humans and pets.

Synonyms[]

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.

Use[]

Starlicide is lethal to starlings with an acute oral LD₅₀ of 3.8 milligrams per kilogram body weight, but it is less toxic to most other birds. Grain-eating game birds such as bobwhite quail,^[4] pheasants (Phasianus colchicus) and rooks (Corvus frugilegus)^[5] are also vulnerable. Hawks and mammals are resistant to the poison. Starlings are killed in a slow, "nonviolent" death by uremic poisoning and congestion of major organs.^[6] The effect is 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 starlicide 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 more than 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. African countries use it to control house crows == Other uses== This compound is also is intermediate product in synthesis of other pesticides, such as menid herbicide (3-Chloro-4-methylphenyl)

Ecological impacts[]

Starlicide can and does kill nontarget species of birds that eat at feedlots and other places it is used. However, this rarely occurs because of the places that Starlicide is used. Rusty blackbirds (Euphagus carolinus), once an abundant species that is declining precipitously, have been theorized to be declining as a result of the use of Starlicide. However, this issue has been analyzed and found to be non-significant and not discussed by Avery (2013).^[14] Rusty blackbirds primarily feed on invertebrates in wet woodlands and near streams throughout the year. Even though they roost with other blackbirds, Rusty Blackbirds usually will not feed with them. Rusty blackbirds are a species not likely to be taken protecting crops because they mostly feed in wet woodland bottoms on acorns, pine seeds, fruits, and animal matter during winter, but sometimes will be found in feedlots (Avery 2013). Even at the highest potential nontarget take with Starlicide, few, if any, would be taken and not a cause a decline in their population. Habitat issues, possibly on their Canadian breeding habitat and on wintering grounds in the southeastern United States such as the decline of wetlands, is likely the primary reason for their decline. But, as poisoned birds may fly long distance before they die, it's difficult to find carcasses and results of studies may underestimate mortality, this had been shown in studying effectiveness of poison to control ravens.

See also[]

• Diclofenac

References[]