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3,4-Pyridinedicarboxylic acid - 98%, high purity , CAS No.490-11-9

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3,4-Pyridinedicarboxylic acid - 98%, high purity , CAS No.490-11-9

2 Citations

COA

Grade & Purity:

≥98%

Cas Number: 490-11-9
Molecular Weight: 167.12
Beilstein Registry Number: 137242
EC Number: 207-705-4
MDL number: MFCD00006392
PubChem CID: 10273
PubChem SID: 488181101

In stock

Item Number

P106870

Grouped product items
SKU	Size	Availability	Price
P106870-5g	5g	3	$40.90
P106870-25g	25g	1	$183.90
P106870-100g	100g	3	$661.90
P106870-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$2,977.90

View related series

carboxylic acid (2098) Organic linker molecule (58)

Basic Description

Synonyms	3,4-Pyridinedicarboxylicacid \| AC-1183 \| FT-0623820 \| Q27120712 \| SCHEMBL71335 \| CL0113 \| Cinchomeronsaure \| NSC178 \| NSC-178 \| CINCHOMERONIC ACID [MI] \| Z1123696308 \| EINECS 207-705-4 \| F0001-1280 \| 3,4-Pyridinedicarboxylic acid \| 3,4-pyridine-dicarboxyl
Specifications & Purity	≥98%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pyridines and derivatives
    - Subclass Pyridinecarboxylic acids and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pyridines and derivatives
Subclass	Pyridinecarboxylic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Pyridinecarboxylic acids
Alternative Parents	Dicarboxylic acids and derivatives Heteroaromatic compounds Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Pyridine carboxylic acid - Dicarboxylic acid or derivatives - Heteroaromatic compound - Azacycle - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group.
External Descriptors	pyridinedicarboxylic acid
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

Associated Targets(non-human)

blaZ Beta-lactamase (285 Activities)

Discover Target: blaZ

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

Beta-lactamase L1 (242 Activities)

Explore this target

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

Pubchem Sid	488181101
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488181101
IUPAC Name	pyridine-3,4-dicarboxylic acid
INCHI	InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-3-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChIKey	MUYSADWCWFFZKR-UHFFFAOYSA-N
Smiles	C1=CN=CC(=C1C(=O)O)C(=O)O
Isomeric SMILES	C1=CN=CC(=C1C(=O)O)C(=O)O
WGK Germany	3
Molecular Weight	167.12
Beilstein	137242
Reaxy-Rn	137242
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=137242&ln=

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.

4 results found

Lot Number	Certificate Type	Date	Item
K2026072	Certificate of Analysis	Sep 14, 2024	P106870
A2521202	Certificate of Analysis	Jul 02, 2024	P106870
A2509233	Certificate of Analysis	Jul 02, 2024	P106870
G1809087	Certificate of Analysis	May 13, 2022	P106870

Chemical and Physical Properties

Solubility	Solubility in 1mol/L NaOH almost transparency
Melt Point(°C)	262-270°C
Molecular Weight	167.120 g/mol
XLogP3	-0.100
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	2
Exact Mass	167.022 Da
Monoisotopic Mass	167.022 Da
Topological Polar Surface Area	87.500 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	204.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Lei Ge, Yang Wang, Xiang Gao, Min Li, Runqi Zhang, Siyu Liu, Yihang Yu, Mingguang Li, Ligang Xu, Ye Tao, Runfeng Chen, Wenzhen Lv. (2022) Stimulating Efficient and Stable Ultralong Phosphorescence of 2D Perovskites by Dual-Mode Triplet Exciton Stabilization. CHEMISTRY OF MATERIALS, 34 (19): (8917–8924).
2. Ru-Ru Gao, Wei Dong. (2021) ATP and lanthanide ions derived coordination polymer nanoparticles as a novel family of versatile materials: Color-tunable emission, artificial tongues and logic devices. MICROCHEMICAL JOURNAL, 160 (105753).

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