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Pterine-6-carboxylic acid - ≥98%, high purity , CAS No.948-60-7

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Pterine-6-carboxylic acid - ≥98%, high purity , CAS No.948-60-7

COA

Grade & Purity:

≥98%

Cas Number: 948-60-7
Molecular Weight: 207.15
Beilstein Registry Number: 227689
EC Number: 213-435-8
PubChem CID: 135403803

In stock

Item Number

P330569

Grouped product items
SKU	Size	Availability	Price
P330569-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$29.90
P330569-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$69.90
P330569-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$179.90

View related series

Pyrazine compounds (41)

Basic Description

Synonyms	6-Pteridinecarboxylic acid, 2-amino-1,4-dihydro-4-oxo- \| HHS \| 2,3,7,8-tetrahydroxy[1]benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione \| KBio2_003290 \| NSC 96893 \| 2-amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid \| 2-amino-4-oxo-3,4-dihydropteridine-6-c
Specifications & Purity	≥98%
Storage Temp	Protected from light,Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Pterine-6-carboxylic acid (6-Carboxypterin) is a photodegradation product of folic acid, which can be used as a photosensitive agent to study the molecular mechanism of UVA breaking DNA structure. Application： Pterine-6-carboxylic Acid is a degradation product of Folic acid.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pteridines and derivatives
    - Subclass Pterins and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pteridines and derivatives
Subclass	Pterins and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Pterin carboxylates
Alternative Parents	Pyrazine carboxylic acids Hydroxypyrimidines Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Pterin-6-carboxylate - Pyrazine carboxylic acid - Pyrazine carboxylic acid or derivatives - Hydroxypyrimidine - Pyrimidine - Pyrazine - Heteroaromatic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as pterin carboxylates. These are heterocyclic aromatic compounds containing a pterin moiety, in which one ring is substituted by one or more carboxylic acid groups. Pterin is a heterocyclic compound composed of a pteridine ring system (made up of a pyrazine fused to a pyrimidine), with a keto group and an amino group at the 2- and 4- positions, respectively.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Product Properties

pKa	pKₐ: 2.82 (Predicted), pKₐ: 0.91 (Predicted)

Associated Targets(Human)

AKR1B1 Tclin Aldose reductase (1404 Activities)

Discover Target: AKR1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

folP Dihydropteroate synthase (129 Activities)

Discover Target: folP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	2-amino-4-oxo-3H-pteridine-6-carboxylic acid
INCHI	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	C1=C(N=C2C(=O)NC(=NC2=N1)N)C(=O)O
Isomeric SMILES	C1=C(N=C2C(=O)NC(=NC2=N1)N)C(=O)O
WGK Germany	3
PubChem CID	135403803
Molecular Weight	207.15
Beilstein	227689

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot Number	Certificate Type	Date	Item
G2502359	Certificate of Analysis	Jun 20, 2025	P330569
G2502356	Certificate of Analysis	Jun 20, 2025	P330569
G2502353	Certificate of Analysis	Jun 20, 2025	P330569
G2502357	Certificate of Analysis	Jun 20, 2025	P330569
G2502358	Certificate of Analysis	Jun 20, 2025	P330569
G2502361	Certificate of Analysis	Jun 20, 2025	P330569

Chemical and Physical Properties

Solubility	Aqueous Acid (Very Slightly), Aqueous Base (Very Slightly, Heated)
Sensitivity	Moisture sensitive；Light sensitive
Refractive Index	n20D1.95 (Predicted)
Boil Point(°C)	~624.8° C at 760 mmHg (Predicted)
Melt Point(°C)	217.69° C (Predicted)
Molecular Weight	207.150 g/mol
XLogP3	-1.500
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	1
Exact Mass	207.039 Da
Monoisotopic Mass	207.039 Da
Topological Polar Surface Area	131.000 Å²
Heavy Atom Count	15
Formal Charge	0
Complexity	342.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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