C1930
2-Chloro-6-(trichloromethyl)pyridine
≥98%
Sinonimo/i:
Nitrapyrin, 2-Chloro-6-(trichloromethyl)pyridine, CP
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About This Item
Formula empirica (notazione di Hill):
C6H3Cl4N
Numero CAS:
Peso molecolare:
230.91
Beilstein:
1618997
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
agenzia
suitable for SM 5210
Livello qualitativo
Saggio
≥98%
Forma fisica
powder
Solubilità
ethanol: 10 mg/mL, clear, colorless to faintly yellow
Stringa SMILE
Clc1cccc(n1)C(Cl)(Cl)Cl
InChI
1S/C6H3Cl4N/c7-5-3-1-2-4(11-5)6(8,9)10/h1-3H
DCUJJWWUNKIJPH-UHFFFAOYSA-N
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Descrizione generale
2-Chloro-6-(trichloromethyl)pyridine is a chlorinatedheterocyclic compound that belongs to the pyridine family and serves as anactive ingredient found in commercially available nitrogen stabilizers. Iteffectively delays the conversion of ammonium (NH₄⁺) to nitrate (NO₃⁻). Thisprocess enhances nitrogen retention and improves nitrogen use efficiency,ultimately leading to increased crop yields.
Applicazioni
- Biological and chemical nitrification inhibitors exhibited different effects on soil gross N nitrification rate and N(2)O production: a (15)N microcosm study.: This study examines the effects of biological and chemical nitrification inhibitors, including 2-Chloro-6-(trichloromethyl)pyridine, on soil nitrogen processes. The findings highlight the differential impacts on soil nitrogen dynamics and greenhouse gas emissions (Lan et al., 2023).
- Nitrous oxide emissions from manured soils as a function of various nitrification inhibitor rates and soil moisture contents.: This paper explores the relationship between nitrification inhibitor application rates, including 2-Chloro-6-(trichloromethyl)pyridine, and soil moisture on nitrous oxide emissions, providing insights into optimizing inhibitor use for environmental benefits (Lin and Hernandez-Ramirez, 2020).
- Nitrate losses in subsurface drainage from a corn-soybean rotation as affected by fall and spring application of nitrogen and nitrapyrin.: Investigating the seasonal application of nitrapyrin, a derivative of 2-Chloro-6-(trichloromethyl)pyridine, this study assesses its efficacy in reducing nitrate leaching and improving nitrogen use efficiency in agricultural systems (Randall and Vetsch, 2005).
- Oxidation of Nitrapyrin to 6-Chloropicolinic Acid by the Ammonia-Oxidizing Bacterium Nitrosomonas europaea.: This foundational research elucidates the microbial degradation pathway of nitrapyrin, contributing to our understanding of its environmental fate and persistence (Vannelli and Hooper, 1992).
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2
Codice della classe di stoccaggio
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
212.0 °F - closed cup
Punto d’infiammabilità (°C)
100 °C - closed cup
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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I clienti hanno visto anche
S J Powell et al.
Journal of general microbiology, 137(8), 1923-1929 (1991-08-01)
Nitrate production by Nitrosomonas europaea in inorganic liquid medium containing ammonium was limited by reduction in pH. In the presence of montmorillonite and vermiculite, expanding clays with high cation-exchange-capacity (CEC), nitrite yield was increased, ammonia oxidation continued at pH values
Q R Shen et al.
Chemosphere, 50(6), 747-753 (2003-04-12)
Because low concentration of nitrite could be toxic to biological systems and high amounts of nitrite have been observed in a river of northern China since 1990, nitrite from agricultural soil sources should be investigated. In this paper, effects of
Distribution of nitrapyrin [12-chloro-6-(trichloromethyl)-pyridine] and 2-chloro-6-(dichloromethyl)-pyridine in red beet treated with nitrapyrin.
H Kallio et al.
Journal of the science of food and agriculture, 33(5), 451-455 (1982-05-01)
N M Berdasco et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 11(3), 464-471 (1988-10-01)
Pregnant Fischer 344 rats and New Zealand White rabbits were orally administered 0, 5, 15, or 50 mg nitrapyrin/kg/day on Gestation Days 6 through 15 (rats) or 0, 3, 10, or 30 mg/kg/day on Gestation Days 6 through 18 (rabbits).
B L Yano et al.
Regulatory toxicology and pharmacology : RTP, 51(1), 53-65 (2008-03-28)
Nitrapyrin has been registered as a nitrogen stabilizer in the United States for many years based on a robust set of regulatory data. These data demonstrated that nitrapyrin was not genotoxic and that there were no tumors elicited in rats
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