Quinine
90%
Manufacturer: Sigma Aldrich
CAS Number: 130-95-0
Synonym(S): 6′-Methoxycinchonidine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 G | 145904-10-G | In Stock | ₹ 4,438.25 |
| 50 G | 145904-50-G | In Stock | ₹ 10,153.85 |
145904 - 10 G
In Stock
Quantity
1
Base Price: ₹ 4,438.25
GST (18%): ₹ 798.885
Total Price: ₹ 5,237.135
Quality Level
200
Assay
90%
optical activity
[α]25/D −165°, c = 2 in ethanol
mp
173-175 °C (lit.)
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)
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | TraceCERT™ Quinine, MilliporeSigma™ Supelco™ | MilliporeSigma Supelco | ₹ 14,177.29 | |
 | eMolecules Quinine | 130-95-0 | | 1g | eMolecules | ₹ 2,416.21 | |
 | Sigma Aldrich Fine Chemicals Biosciences Quinine suitable for fluorescence, anhydrous, >=98.0% (dried material, NT) | 130-95-0 | MFCD00198096 | 5G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 9,296.95 | |
| | eMolecules Medchem Express / Quinine / 500mg / 491484691 / HY-D0143 / / 130-95-0 / [null] / 324.424 / C20H24N2O2 | eMolecules | ₹ 6,297.22 | |
 | eMolecules (R)-[(2S,4S,5R)-1-Aza-5-vinylbicyclo[2.2.2]oct-2-yl](6-methoxyquinolin-4-yl)methanol | 130-95-0 | MFCD00198096 | 1g | eMolecules | ₹ 2,678.03 | |
 | Quinine | Supelco | ₹ 11,896.68 | |
| | (-)-Quinine | Sigma Aldrich | ₹ 28,047.58 | |
 | (-)-Quinine | Sigma Aldrich | ₹ 7,720.00 | |
 | Quinine | ChemScene | ₹ 770.04 - ₹ 45,945.72 |
Related Products
Description
- 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
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 200
Assay: 90%
optical activity: [α]25/D −165°, c = 2 in ethanol
mp: 173-175 °C (lit.)
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)
Quality Level: 500
Assay: __
optical activity: __
mp: __
SMILES string: __
InChI: __
InChI key: __
Gene Information: __
Quality Level: 100
Assay: 90%
optical activity: [α]20/D −144°, c = 1 in H2O
mp: 115-116 °C (dec.) (lit.)
SMILES string: Cl[H].[H]O[H].[H]O[H].[H][C@@]12CCN(C[C@@H]1C=C)[C@@]([H])(C2)[C@H](O)c3ccnc4ccc(OC)cc34
InChI: 1S/C20H24N2O2.ClH.2H2O/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;1H;2*1H2/t13-,14-,19-,20+;;;/m0.../s1
InChI key: MPQKYZPYCSTMEI-FLZPLBAKSA-N
Gene Information: __
