Product 145904 should be stored at ambient temperature in a dark place due to its light sensitivity. The Flinn compatibility storage code (TRGS 510) for this item is 11, indicating it is a combustible solid.
145904
Quinine
90%
Sinónimos:
6′-Methoxycinchonidine
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10 G
MXP 2,111.00
50 G
MXP 7,280.00
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10 G
MXP 2,111.00
50 G
MXP 7,280.00
About This Item
Fórmula empírica (notación de Hill):
C20H24N2O2
Número de CAS:
Peso molecular:
324.42
Beilstein/REAXYS Number:
91867
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
90%
optical activity
[α]25/D −165°, c = 2 in ethanol
mp
173-175 °C (lit.)
functional group
hydroxyl
SMILES string
COc1ccc2nccc([C@@H](O)[C@@H]3C[C@@H]4CCN3C[C@@H]4C=C)c2c1
InChI
1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19-,20+/m0/s1
InChI key
LOUPRKONTZGTKE-WZBLMQSHSA-N
Gene Information
human ... ABCB1(5243) , CYP2C9(1559) , CYP2D6(1565)
rat ... Cyp2d1(266684) , Cyp2d2(25053) , Cyp2d3(24303) , Cyp2d4v1(171522)
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General description
Quinine, a cinchona alkaloid found in the bark of the cinchona tree, is known for its anti-malarial property.[1]
Application
Quinine has been used as a standard during the chemical evaluation of alkaloids in the hydroethanolic extracts of endophytic fungi obtained from the leaves of Costus spiralis by TLC.[2]
Biochem/physiol Actions
Potassium channel blocker
Other Notes
remainder hydroquinine
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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