| Identification | More | [Name]
XANTHURENIC ACID | [CAS]
59-00-7 | [Synonyms]
4,8-DIHYDROXY-2-QUINOLINECARBOXYLIC ACID
4,8-DIHYDROXYQUINALDIC ACID
4,8-DIHYDROXYQUINOLINE-2
4,8-DIHYDROXYQUINOLINE-2-CARBOXYLIC ACID
TIMTEC-BB SBB003498
XANTHURENIC ACID
XANTHURIC ACID
XENTHURENIC ACID
4,8-dihydroxy-2-quinolinecarboxylicaci
4,8-dihydroxy-quinaldicaci
4,8-dihydroxyquinaldinicacid
8-hydroxykynurenicacid
2-Quinolinecarboxylic acid, 4,8-dihydroxy-
XANTHURENIC ACID(RG)
4,8-DIHYDROXYQUINOLINE-2-CARBOXYLIC ACID 96%
XANTHURENIC ACID extrapure
4,8-Dihydroxyquinaldic acid, 4,8-Dihydroxyquinoline-2-carboxylic acid | [EINECS(EC#)]
200-410-1 | [Molecular Formula]
C10H7NO4 | [MDL Number]
MFCD00006754 | [Molecular Weight]
205.17 | [MOL File]
59-00-7.mol |
| Chemical Properties | Back Directory | [Appearance]
ochre powder | [Melting point ]
297-298 °C (dec.)(lit.) | [Boiling point ]
343.83°C (rough estimate) | [density ]
1.3849 (rough estimate) | [refractive index ]
1.5600 (estimate) | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
DMSO (Slightly, Heated), Water (Slightly, Heated) | [form ]
Powder | [pka]
1.20±0.30(Predicted) | [color ]
Ochre | [Merck ]
10068 | [BRN ]
185954 | [CAS DataBase Reference]
59-00-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
UZ9275000
| [HS Code ]
29334900 |
| Hazard Information | Back Directory | [Chemical Properties]
ochre powder | [Uses]
Xanthurenic acid can be used as a substrate for the synthesis of:
- Silica-gel functionalized xanthurenic acid (4, 8-dihydroxyquinoline-2-carboxylic acid) as an adsorbent for metal ions.
- N, N′-bis-((8-hydroxy-7-quinolinyl)methyl)-1,10-diaza-18-crown-6 ethers as fluorescent sensors of magnesium in living cells via one-pot Mannich reaction.
- Poly-xanthurenic acid (poly-Xa) for biosensing applications.
| [Uses]
caspase activator, guanylyl cyclase stimulant | [Uses]
Excreted by pyridoxine-deficient animals after the ingestion of tryptophan. | [Definition]
ChEBI: A quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by hydroxy groups at C-4 and C-8. | [storage]
Room temperature | [Purification Methods]
It is precipitated by the addition of 2N formic acid to its solution in hot 2M ammonia (charcoal). The solid is filtered off, dried in a vacuum at ~80o in the dark. UV (H2O) has nm ( M-1cm-1): 243 (30,000) and 342 (6,500). The methyl ester has m 262o (from MeOH). It forms Cu2+, Zn2+, Fe2+ and Fe3+ salts. [Beilstein 22 III/IV 2513.] |
|
|