2,5-Pyridinedicarboxylic acid - 98%, high purity , CAS No.100-26-5

2 Citations
  • ≥98%
Item Number
P106867
Grouped product items
SKUSizeAvailabilityPrice Qty
P106867-5g
5g
In stock
$30.90
P106867-25g
25g
In stock
$118.90
P106867-100g
100g
In stock
$427.90

Basic Description

Synonyms6-carboxy-nicotinic acid | 1189695-39-3 | AM20050593 | FG-0457 | SY007555 | F0001-0013 | 2,5-Pyridinedicarboxylic acid | AB00376873-03 | pyridine carboxylate, 6b | AKOS000119637 | NCGC00336418-01 | W-204355 | Pyridinedicarboxylic acid-(2,5) | PYRIDINE-2,5
Specifications & Purity≥98%
Shipped InNormal
Product Description

2,5-Pyridinedicarboxylic acid is used to prepare new 2,5-pyridinedicarboxylic acid derivatives as antiviral agents.
An intermediate for antiviral agents.

2,5-Pyridinedicarboxylic acid can be used:

• In the synthesis of diorganotin(IV) 2,5-pyridinedicarboxylates.

• In the preparation of three-dimensional coordination polymers of lanthanide 2,5-pyridinedicarboxylates by hydrothermal method.

• As an organocatalyst in the synthesis of 1,5-benzodiazepine derivatives via one pot three-component reaction.

Associated Targets(Human)

EGLN1 Tclin Egl nine homolog 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EGLN3 Tclin Egl nine homolog 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EGLN2 Tclin Egl nine homolog 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP1 Tchem Interstitial collagenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP9 Tchem Matrix metalloproteinase-9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX5 Tclin Arachidonate 5-lipoxygenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP2 Tchem 72 kDa type IV collagenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
P4HA1 Tchem Prolyl 4-hydroxylase subunit alpha-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
P4HTM Tchem Transmembrane prolyl 4-hydroxylase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NOS2 Tchem Nitric oxide synthase, inducible (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KDM4E Tchem Lysine-specific demethylase 4E (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP3 Tchem Stromelysin-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP8 Tchem Neutrophil collagenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGLN2 Tclin Hypoxia-inducible factor prolyl hydroxylase 1 (404 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MMP3 Tchem Matrix metalloproteinase 3 (3433 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MMP8 Tchem Matrix metalloproteinase 8 (1942 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P4HTM Tchem Hypoxia-inducible factor prolyl 4-hydroxylase (111 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MMP1 Tchem Matrix metalloproteinase-1 (7046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGLN1 Tclin Egl nine homolog 1 (1702 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGLN3 Tclin Egl nine homolog 3 (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P4HA1 Tchem Prolyl 4-hydroxylase subunit alpha-1 (16 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

blaZ Beta-lactamase (285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp2 Matrix metalloproteinase-2 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P4ha1 Prolyl 4-hydroxylase alpha-1 subunit (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Beta-lactamase L1 (242 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
blaIMP-1 Metallo beta-lactamase (43 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488180462
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180462
IUPAC Name pyridine-2,5-dicarboxylic acid
INCHI InChI=1S/C7H5NO4/c9-6(10)4-1-2-5(7(11)12)8-3-4/h1-3H,(H,9,10)(H,11,12)
InChi Key LVPMIMZXDYBCDF-UHFFFAOYSA-N
Canonical SMILES C1=CC(=NC=C1C(=O)O)C(=O)O
Isomeric SMILES C1=CC(=NC=C1C(=O)O)C(=O)O
WGK Germany 3
PubChem CID 7493
Molecular Weight 167.12
Beilstein 131697
Reaxy-Rn 131697

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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

6 results found

Lot NumberCertificate TypeDateItem
A2411005Certificate of AnalysisAug 08, 2022 P106867
D2324720Certificate of AnalysisAug 08, 2022 P106867
D2426043Certificate of AnalysisAug 08, 2022 P106867
I2214246Certificate of AnalysisAug 08, 2022 P106867
I2214248Certificate of AnalysisAug 08, 2022 P106867
I2214251Certificate of AnalysisAug 08, 2022 P106867

Chemical and Physical Properties

Melt Point(°C)254 °C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

WGK Germany 3
Reaxy-Rn 131697
Merck Index 5159

Related Documents

Citations of This Product

1. Zhiyuan Liu, Linmeng Wang, Changan Wang, Rushuo Li, Peiyun Zhou, Hongyi Gao, Ge Wang.  (2024)  Modulating the strong metal-support interactions by regulating the chemical microenvironment of Pt confined in MOFs for low temperature hydrogenation of DCPD.  CHEMICAL ENGINEERING JOURNAL,  479  (147601).  [PMID:]
2. Li-Qiong He, Zhi-Mei Wang, Yu-Jie Li, Jing Yang, Li-Fu Liao, Xi-Lin Xiao, Yong Liu.  (2022)  A Novel Electrochemical Sensor Modified with a Computer-Simulative Magnetic Ion-Imprinted Membrane for Identification of Uranyl Ion.  SENSORS,  22  (12): (4410).  [PMID:35746190]

References

1. Rose NR, Ng SS, Mecinović J, Liénard BM, Bello SH, Sun Z, McDonough MA, Oppermann U, Schofield CJ.  (2008)  Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases..  J Med Chem,  51  (22): (7053-6).  [PMID:18942826]
2. L E Horsfall,G Garau,B M R Liénard,O Dideberg,C J Schofield,J M Frère,M Galleni.  (2007-02-20)  Competitive inhibitors of the CphA metallo-beta-lactamase from Aeromonas hydrophila..  Antimicrobial agents and chemotherapy,  51  ((6)): (2136-2142).  [PMID:17307979]
3. Jennifer A Jacobsen,Jessica L Fullagar,Melissa T Miller,Seth M Cohen.  (2010-12-30)  Identifying chelators for metalloprotein inhibitors using a fragment-based approach..  Journal of medicinal chemistry,  54  ((2)): (591-602).  [PMID:21189019]
4. Debal Kanti Singha,Partha Mahata.  (2017-08-16)  Coordination polymer-derived nano-sized zinc ferrite with excellent performance in nitro-explosive detection..  Dalton transactions (Cambridge, England : 2003),  46  ((34)): (11344-11354).  [PMID:28809982]
5. Athanasios Koutsianos,Ewa Kazimierska,Andrew R Barron,Marco Taddei,Enrico Andreoli.  (2019-02-20)  A new approach to enhancing the CO2 capture performance of defective UiO-66 via post-synthetic defect exchange..  Dalton transactions (Cambridge, England : 2003),  48  ((10)): (3349-3359).  [PMID:30778497]
6. Noemí Contreras-Pereda,Faezeh Moghzi,Javier Baselga,Haixia Zhong,Jan Janczak,Janet Soleimannejad,Renhao Dong,Daniel Ruiz-Molina.  (2020-08-05)  Ultrasound-assisted exfoliation of a layered 2D coordination polymer with HER electrocatalytic activity..  Ultrasonics sonochemistry,  70  (105292-105292).  [PMID:32750659]
7. Zhiyuan Liu, Linmeng Wang, Changan Wang, Rushuo Li, Peiyun Zhou, Hongyi Gao, Ge Wang.  (2024)  Modulating the strong metal-support interactions by regulating the chemical microenvironment of Pt confined in MOFs for low temperature hydrogenation of DCPD.  CHEMICAL ENGINEERING JOURNAL,  479  (147601).  [PMID:]
8. Li-Qiong He, Zhi-Mei Wang, Yu-Jie Li, Jing Yang, Li-Fu Liao, Xi-Lin Xiao, Yong Liu.  (2022)  A Novel Electrochemical Sensor Modified with a Computer-Simulative Magnetic Ion-Imprinted Membrane for Identification of Uranyl Ion.  SENSORS,  22  (12): (4410).  [PMID:35746190]

Solution Calculators