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Assay
98%
form
crystals
bp
127-128 °C/11 mmHg (lit.)
mp
135-138 °C (lit.)
SMILES string
Nc1ccc(Cl)cn1
InChI
1S/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
InChI key
MAXBVGJEFDMHNV-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
320.0 °F
Flash Point(C)
160 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
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
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
Electrophoresis, 33(11), 1606-1612 (2012-06-28)
A capillary electrophoretic enantioselective method with UV detection was developed and validated for the simultaneous quantification of zopiclone enantiomers and its impurities, zopiclone-N-oxide enantiomers, and 2-amino-5-chloropyridine, in tablets. The analytes were extracted from the tablets using ACN and were separated
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