07530
2-氨基-5-氯吡啶
purum, ≥98.0% (NT)
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关于此项目
经验公式（希尔记法）:
C5H5ClN2
化学文摘社编号:
分子量:
128.56
EC Number:
214-020-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
108735
MDL number:
InChI key
MAXBVGJEFDMHNV-UHFFFAOYSA-N
InChI
1S/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
SMILES string
Nc1ccc(Cl)cn1
grade
purum
assay
≥98.0% (NT)
bp
127-128 °C/11 mmHg (lit.)
mp
135-137 °C, 135-138 °C (lit.)
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
320.0 °F
flash_point_c
160 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
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J H Galloway et al.
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
Gunnel H Nilsson et al.
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
Noreen Bannan et al.
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
N Sundaraganesan et al.
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
Ricarda Jantos et al.
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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