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A79205

Sigma-Aldrich

5-Aminoquinoline

97%

Synonym(s):

5-Quinolinamine

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100 EA
$260.00

$260.00

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100 EA
$260.00

About This Item

Empirical Formula (Hill Notation):
C9H8N2
CAS Number:
611-34-7
Molecular Weight:
144.17
Beilstein/REAXYS Number:
114479
EC Number:
210-266-1
MDL number:
MFCD00006797
UNSPSC Code:
12352100
PubChem Substance ID:
24891293
NACRES:
NA.22

$260.00

Available to ship onApril 01, 2025Details

Request a Bulk Order

assay

97%

form

powder

bp

310 °C (lit.)

mp

106-109 °C (lit.)

SMILES string

Nc1cccc2ncccc12

InChI

1S/C9H8N2/c10-8-4-1-5-9-7(8)3-2-6-11-9/h1-6H,10H2

InChI key

XMIAFAKRAAMSGX-UHFFFAOYSA-N

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agency

suitable for BS EN 15662:2008

agency

suitable for EPA ACB B21-02, suitable for EPA ACB B23-05b

agency

-

agency

suitable for BS EN 15662:2008

product line

Supel™

product line

Supel™

product line

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product line

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composition

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composition

magnesium sulfate, 6 g , sodium chloride, 1 1/2 g

composition

magnesium sulfate, 4 g , sodium chloride, 1 g

composition

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packaging

pack of 100

packaging

pk of 50

packaging

pk of 50

packaging

pack of 100

technique(s)

QuEChERS: suitable

technique(s)

QuEChERS: suitable

technique(s)

QuEChERS: suitable

technique(s)

QuEChERS: suitable

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    STBL4538
    STBJ7007
    STBH2703
    STBH4085
    S74013V

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    V Arjunan et al.
    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(5), 1215-1223 (2009-10-27)
    The Fourier transform infrared (FTIR) and FT-Raman spectra of 5-aminoquinoline (5AQ) have been recorded in the range 4000-400 and 3500-100 cm(-1), respectively. The complete vibrational assignment and analysis of the fundamental modes of the compounds were carried out using the
    R Banoo et al.
    Indian journal of biochemistry & biophysics, 30(4), 229-233 (1993-08-01)
    In vitro oxidation and acetylation of 5-aminoquinoline by rabbit liver enzyme preparation has been investigated. Incubation of 5-aminoquinoline with cytosol fraction of the enzyme preparation in the presence of acetyl coenzyme-A gave rise to three different products, viz. 5-amino-2-hydroxy quinoline
    Jagat P Bridhkoti et al.
    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(3), 412-417 (2011-04-20)
    Photophysical properties of 5-aminoquinoline (5AQ) have been investigated in various non-polar and polar (protic and aprotic) solvents using steady state and time resolved fluorescence. In aprotic solvents, the spectral maxima depend on the polarity. However, in protic solvents both the
    B G Siim et al.
    Biochemical pharmacology, 48(8), 1593-1604 (1994-10-18)
    The 4-alkylamino-5-nitroquinolines (5NQs) are a new series of bioreductive drugs that exhibit varying degrees of selective toxicity (up to 60-fold) under hypoxic conditions in cell culture. This study tested the hypothesis that differences in hypoxia-selective cytotoxicity in this series reflect
    Maria Sittig et al.
    Chemistry (Weinheim an der Bergstrasse, Germany), 27(3), 1072-1079 (2020-09-29)
    Quinoline photobases exhibit a distinctly higher pKa in their electronically excited state than in the ground state, thereby enabling light-controlled proton transfer reactions, for example, in molecular catalysis. The absorption of UV light translates to a pKa jump of approximately
    View All Related Papers

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