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A46803

Sigma-Aldrich

2-Amino-5-chloropyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C5H5ClN2
CAS Number:
1072-98-6
Molecular Weight:
128.56
Beilstein:
108735
EC Number:
214-020-4
MDL number:
MFCD00006324
UNSPSC Code:
12352100
PubChem Substance ID:
24890897
NACRES:
NA.22

Quality Level

100

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

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF2643V
STBK6031
STBJ2020
STBH0384
STBG9971

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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
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
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
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
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
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