- Synthesis of 6-formylpterineZav'yalov, S. I.; Zavozin, A. G., Izvestiya Akademii Nauk SSSR, 1981, (7), 1669-70
Cas no 948-60-7 (Pterine-6-carboxylic Acid)
Pterine-6-carboxylic Acid structure
Product Name:Pterine-6-carboxylic Acid
CAS No:948-60-7
MF:C7H5N5O3
MW:207.146300077438
MDL:MFCD00010594
CID:40392
PubChem ID:57652920
Update Time:2024-10-25
Pterine-6-carboxylic Acid Chemical and Physical Properties
Names and Identifiers
-
- Pterin-6-carboxylic acid
- 2-Amino-1,4-dihydro-4-oxopteridine-6-carboxylic acid
- Pterine-6-carboxylic Acid
- 2-amino-4-oxo-1H-pteridine-6-carboxylic acid
- Pterine-6-carboxylic
- 2-Amino-4-hydroxypteridine-6-carboxylicacid
- 2-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid (ACI)
- 6-Pteridinecarboxylic acid, 2-amino-1,4-dihydro-4-oxo- (8CI, 9CI)
- 6-Pteridinecarboxylic acid, 2-amino-4-hydroxy- (6CI)
- 2-Amino-4-hydroxy-6-carboxypteridine
- 2-Amino-4-hydroxypteridine-6-carboxylic acid
- 2-Amino-4-hydroxypterin-6-carboxylic acid
- 2-Amino-4-oxo-1,4-dihydropteridine-6-carboxylic acid
- 2-Amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid
- 2-Amino-4-oxo-4,8-dihydropteridine-6-carboxylic acid
- 2-Amino-6-carboxy-4-hydroxypteridine
- 2-Imino-4-oxo-1,2,3,4-tetrahydropteridine-6-carboxylic acid
- 6-Carboxypterin
- NSC 96893
- Ranachrome 5
- Spectrum_000242
- 2-Amino-4(3H)-pteridinone-6-carboxylic acid
- HHS
- 1501-50-4
- 2G01J4LZ8Y
- Spectrum4_001713
- KBioGR_002066
- Q27161007
- 2-amino-4-oxo-3,4-dihydropteridine-6-carboxylicacid
- MFCD00010594
- 6-PTERIDINECARBOXYLIC ACID, 2-AMINO-4-HYDROXY-
- SCHEMBL893092
- CHEMBL566727
- SpecPlus_000795
- SCHEMBL13820952
- KBio2_003290
- 2-Amino-1,4-dihydro-4-oxo-6-Pteridinecarboxylic acid
- PTERIN-6-CARBOXYLICACID
- DivK1c_006891
- GEO-04483
- FT-0633615
- 948-60-7
- 2-Amino-4-oxo-3,4-dihydro-6-pteridinecarboxylic acid
- UNII-2G01J4LZ8Y
- KBio2_000722
- 6-Pteridinecarboxylic acid, 2-amino-1,4-dihydro-4-oxo-
- 2-amino-4-hydroxy-6-pteridinecarboxylic acid
- F87135
- 6-car-boxypterin
- CCG-38452
- CS-0094339
- NS00040423
- KBio2_005858
- KBio1_001835
- CHEBI:88937
- NSC96893
- EINECS 213-435-8
- Spectrum5_000446
- Spectrum3_001713
- Spectrum2_001821
- BSPBio_003326
- DTXSID30241626
- 2-Amino-4-oxo-3,4-dihydro-6-pteridinecarboxylic acid #
- QABAUCFGPWONOG-UHFFFAOYSA-N
- 2-AMINO-3,4-DIHYDRO-4-OXO-6-PTERIDINECARBOXYLIC ACID
- 2-AMINO-4-OXO-3H-PTERIDINE-6-CARBOXYLIC ACID
- AKOS015910901
- KBio3_002546
- KBioSS_000722
- A809012
- SPBio_001861
- 2-amino-4-keto-1H-pteridine-6-carboxylic acid
- AKOS040763764
- HY-W037823
- NCGC00178139-01
- Pterine-6-carboxylic acid, >=98.0% (HPLC)
- NSC-96893
- DB-043039
- DA-66999
- 6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo-
-
- MDL： MFCD00010594
- 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)
- InChI Key： QABAUCFGPWONOG-UHFFFAOYSA-N
- SMILES： O=C(C1=CNC2C(C(N=C(N)N=2)=O)=N1)O
Computed Properties
- Exact Mass: 207.039
- Monoisotopic Mass: 207.039
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 15
- Rotatable Bond Count: 1
- Complexity: 342
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 131A^2
- Surface Charge: 0
- Tautomer Count: 18
- XLogP3: -1.5
Experimental Properties
- Density: 2.16 g/cm3
- Boiling Point: 608.7oC at 760 mmHg
- Flash Point: 322oC
- Refractive Index: 1.954
Pterine-6-carboxylic Acid Security Information
- Hazardous Material transportation number：NONH for all modes of transport
- WGK Germany：3
- Safety Instruction： 22-24/25
- FLUKA BRAND F CODES：10
- Storage Condition：2-8°C
Pterine-6-carboxylic Acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM332737-1g |
2-Amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid |
948-60-7 | 95%+ | 1g |
$1578 | 2021-08-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA04692-100mg |
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Pterine-6-carboxylic Acid |
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￥1973.48 | 2023-10-02 | ||
| TRC | P839880-100mg |
Pterine-6-carboxylic Acid |
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$ 215.00 | 2023-09-06 | ||
| TRC | P839880-1g |
Pterine-6-carboxylic Acid |
948-60-7 | 1g |
$ 1805.00 | 2023-09-06 | ||
| A2B Chem LLC | AA75385-5mg |
6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo- |
948-60-7 | 99% | 5mg |
$385.00 | 2024-07-18 | |
| A2B Chem LLC | AA75385-25mg |
6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo- |
948-60-7 | 99% | 25mg |
$1025.00 | 2024-07-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1164979-100mg |
Pterin-6-carboxylic acid |
948-60-7 | 97% | 100mg |
￥1644.00 | 2024-04-24 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1164979-250mg |
Pterin-6-carboxylic acid |
948-60-7 | 97% | 250mg |
￥3460.00 | 2024-04-24 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1164979-1g |
Pterin-6-carboxylic acid |
948-60-7 | 97% | 1g |
￥13657.00 | 2024-04-24 |
Pterine-6-carboxylic Acid Production Method
Production Method 1
Production Method 2
Production Method 3
Reaction Conditions
Reference
- Analysis of the preliminary radiolytic products of folic acidYan, Yueren; Tang, Benlian; Bai, Hong, Shipin Yu Fajiao Gongye, 1987, (5), 30-4
Production Method 4
Reaction Conditions
Reference
- Qualitative demonstration of the degradation of folic acid by Pseudomonas fluorescens UK-1Soini, Juhani; Majasaari, Karin, Acta Chemica Scandinavica (1947-1973), 1973, 27(6), 2115-20
Production Method 5
Reaction Conditions
Reference
- Preparation of isotope-labeled dihydroneopterin 3'-triphosphate with high specific activityKatzenmeier, Gerd; Schwarzkopf, Bruno; Le Van Quang; Schmid, Cornelia; Bacher, Adelbert, Pteridines, 1991, 2(3), 169-74
Production Method 6
Reaction Conditions
Reference
- Pteridines. XXXIX. Synthesis and structure of pterin-6- and -7-carboxylic acidsPfleiderer, Wolfgang; Zondler, Helmut; Mengel, Rudolf, Justus Liebigs Annalen der Chemie, 1970, 741, 64-78
Production Method 7
Reaction Conditions
1.1 Reagents: Oxygen Solvents: Water
Reference
- Photochemistry of dihydrobiopterin in aqueous solutionVignoni, Mariana; Cabrerizo, Franco M.; Lorente, Carolina; Claparols, Catherine; Oliveros, Esther; et al, Organic & Biomolecular Chemistry, 2010, 8(4), 800-810
Production Method 8
Production Method 9
Reaction Conditions
1.1 Reagents: Oxygen
Reference
- Encapsulation of folic acid (vitamin B6) into sporopollenin microcapsules: Physico-chemical characterisation, in vitro controlled release and photoprotection studyMohammed, Al-Shymaa Y.; Dyab, Amro K. F.; Taha, Fouad; Abd El-Mageed, Ahmed I. A., Materials Science & Engineering, 2021, 128,
Production Method 10
Reaction Conditions
1.1 Solvents: Water ; pH 7, rt
Reference
- Photo-oxidation of sepiapterin produces pterin-6-carboxylic acid and H2O2 in vitroRokos, H.; Schallreuter, K. U., Chemistry and Biology of Pteridines and Folates, 2002, 55, 55-59
Production Method 11
Production Method 12
Reaction Conditions
Reference
- Pteridines, LXVI. Synthesis and properties of dihydro- and tetrahydro derivatives of pterin-6,7-dicarboxylic acidMengel, Rudolf; Pfleiderer, Wolfgang, Chemische Berichte, 1978, 111(12), 3790-805
Production Method 13
Reaction Conditions
Reference
- Synthesis of pteridine-6-carboxamides. 9-Oxofolic acid and 9-oxoaminopterinNair, M. G.; Baugh, Charles M., Journal of Organic Chemistry, 1973, 38(12), 2185-9
Production Method 14
Reaction Conditions
1.1 Reagents: Oxygen Solvents: Water
Reference
- Shelter for Biologically Relevant Molecules: Photoprotection and Enhanced Thermal Stability of Folic Acid Loaded in a ZIF-8 MOF Porous HostTuninetti, Jimena S. ; Serrano, Mariana P. ; Thomas, Andres ; Azzaroni, Omar ; Rafti, Matias, Industrial & Engineering Chemistry Research, 2020, 59(51), 22155-22162
Production Method 15
Reaction Conditions
1.1 Reagents: Oxygen Solvents: Water ; pH 5.5
Reference
- New results on the photochemistry of biopterin and neopterin in aqueous solutionVignoni, Mariana; Cabrerizo, Franco M.; Lorente, Carolina; Thomas, Andres H., Photochemistry and Photobiology, 2009, 85(1), 365-373
Production Method 16
Reaction Conditions
1.1 Solvents: Water ; 8 h
Reference
- Possible role of hydroxyl radicals in the oxidative degradation of folic acidPatro, Birija S.; Adhikari, Soumyakanti; Mukherjee, Tulsi; Chattopadhyay, Subrata, Bioorganic & Medicinal Chemistry Letters, 2005, 15(1), 67-71
Pterine-6-carboxylic Acid Raw materials
- D-Neopterin
- L-Sepiapterin
- 2,4-Diaminopteridine-6-carboxylic Acid
- 2-[(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid
- 6,7-Pteridinedicarboxylic acid, 2-amino-1,4-dihydro-4-oxo-
- Folic acid
- 6-Pteridinecarboxaldehyde,2-amino-3,4-dihydro-4-oxo-
- 7,8-Dihydro-L-biopterin
Pterine-6-carboxylic Acid Preparation Products
Pterine-6-carboxylic Acid Related Literature
-
Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
-
M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
-
Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
-
Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
-
Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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