A46803
2-Amino-5-chloropyridine
98%
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About This Item
Prodotti consigliati
Livello qualitativo
Saggio
98%
Forma fisica
crystals
P. eboll.
127-128 °C/11 mmHg (lit.)
Punto di fusione
135-138 °C (lit.)
Stringa SMILE
Nc1ccc(Cl)cn1
InChI
1S/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
MAXBVGJEFDMHNV-UHFFFAOYSA-N
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Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
320.0 °F
Punto d’infiammabilità (°C)
160 °C
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Drug and alcohol review, 26(1), 83-85 (2007-03-17)
The prevalence of zopiclone misuse in clients attending a methadone maintenance programme in Dublin through detection of its degradation product, 2-amino-5-chloropyridine (ACP) on urinalysis is outlined. Urine samples from all 158 clients were tested for the presence of ACP, opiates
Science & justice : journal of the Forensic Science Society, 39(4), 253-256 (2000-05-05)
Zopiclone (Zimovane) is a cyclopyrrolone compound which exhibits hypnotic and sedative effects while also exhibiting anticonvulsant and muscle relaxant activities. The detection and quantification of zopiclone is difficult. It has a high molecular weight compared to most other commonly used
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(3), 586-594 (2006-01-03)
The FTIR and FT-Raman spectra of 2-amino-5-chloropyridine (ACP) has been recorded in the region 4000-400 and 3500-100 cm-1, respectively. The optimized geometry, frequency and intensity of the vibrational bands of ACP were obtained by the ab initio and density functional
Forensic science international, 200(1-3), 130-135 (2010-05-04)
Zopiclone is a common drug in forensic cases and it is frequently analyzed in biological materials using different analytical methods. Zopiclone is unstable in certain solvents and depending on storage conditions unstable in biological fluids; however its stability in human
International journal of legal medicine, 127(1), 69-76 (2012-04-26)
Z-drugs such as zopiclone are increasingly involved in forensic cases. Its degradation occurs in solvents and biological fluids. It is assumed that hydrolysis largely accounts for the breakdown of zopiclone in aqueous media. Therefore, a stability study in blood at
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