| Identification | Back Directory | [Name]
Pterin-6-carboxylic acid | [CAS]
948-60-7 | [Synonyms]
Folic Acid Impurity 45
PTERIN-6-CARBOXYLIC ACID
PTERINE-6-CARBOXYLIC ACID
2-amino-4-oxo-1H-pteridine-6-carboxylicaci
2-AMINO-4-HYDROXYPTERIDINE-6-CARBOXYLIC ACID
2-amino-4-oxo-1H-pteridine-6-carboxylic acid
2-azanyl-4-oxo-1H-pteridine-6-carboxylic acid
2-amino-4-keto-1H-pteridine-6-carboxylic acid
2-amino-1,4-dihydro-4-oxopteridine-6-carboxylic acid
2-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid
2-amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid
6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo-
Pterine-6-carboxylic acid,2-Amino-4-hydroxypteridine-6-carboxylicacid | [EINECS(EC#)]
213-435-8 | [Molecular Formula]
C7H5N5O3 | [MDL Number]
MFCD00010594 | [MOL File]
948-60-7.mol | [Molecular Weight]
207.15 |
| Chemical Properties | Back Directory | [Melting point ]
300 °C (approx, decomp) | [Boiling point ]
433.6±55.0 °C(Predicted) | [density ]
2.16±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Aqueous Acid (Very Slightly), Aqueous Base (Very Slightly, Heated) | [form ]
Solid | [pka]
5.40±0.20(Predicted) | [color ]
Yellow to Dark Yellow | [biological source]
synthetic | [BRN ]
227689 | [Stability:]
Hygroscopic | [InChI]
1S/C7H5N5O3/c8-7-11-4-3(5(13)12-7)10-2(1-9-4)6(14)15/h1H,(H,14,15)(H3,8,9,11,12,13) | [InChIKey]
QABAUCFGPWONOG-UHFFFAOYSA-N | [SMILES]
NC1=Nc2ncc(nc2C(=O)N1)C(O)=O | [NIST Chemistry Reference]
Pterin-6-carboxylic acid(948-60-7) |
| Hazard Information | Back Directory | [Uses]
Pterine-6-carboxylic Acid is a degradation product of Folic acid (F680300). | [Definition]
ChEBI: 2-Amino-4-hydroxy-6-pteridinecarboxylic acid is an organooxygen compound and an organonitrogen compound. It is functionally related to an alpha-amino acid. | [Purification Methods]
The acid gives yellow crystals by repeated dissolution in aqueous NaOH and adding aqueous HCl. It has UV with max at 235, 260 and 265nm ( 11,000, 10,500 and 9,000) in 0.1N HCl and 263 and 365nm ( 20,500 and 9,000) in 0.1N NaOH. [UV: Pfleiderer et al. Justus Liebigs Ann Chem 741 64 1970, Stockstad et al. J Am Chem Soc 70 5 1948, Fluorescence: Kavanagh & Goodwin Arch Biochem 20 315 1949, Beilstein 26 III/IV 4053.] |
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