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1H-Imidazole-4-carboxylic acid - 98%, high purity , CAS No.1072-84-0

1 Citations

COA

Grade & Purity:

≥98%

Cas Number: 1072-84-0
Molecular Weight: 112.09
Beilstein Registry Number: 25(3/4)720
EC Number: 214-017-8
MDL number: MFCD00082203
PubChem CID: 14080
PubChem SID: 504752520

In stock

Item Number

I111403

Grouped product items
SKU	Size	Availability	Price
I111403-250mg	250mg	≥10	$9.90
I111403-1g	1g	5	$19.90
I111403-5g	5g	3	$66.90
I111403-10g	10g	1	$93.90
I111403-25g	25g	2	$163.90
I111403-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$459.90

View related series

Five-Membered Heterocyclic Compounds (2064) Imidazoles (222)

Basic Description

Synonyms	IMIDAZOLE-4(OR 5)-CARBOXYLIC ACID \| imidazole-5-carboxylic acid \| NSC32340 \| NSC-32340 \| BB 0254749 \| F1791-0473 \| PB47477 \| TS-01557 \| AKOS008105105 \| BCP05792 \| 4-Imidazolecarboxylic acid \| 4-imidazole-carboxylic acid \| NSC 32340 \| EINECS 214-017-8 \| 1H
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	4-Imidazolecarboxylic acid (1H-imidazole-4-carboxylic acid, H2imc) is an imidazole derivative that contains an imidazole group and a carboxylate group. It has been widely utilized to generate different types of coordination polymers. The anion of 4-imidazolecarboxylic acid has been reported to stabilize binuclear hydroxo complexes of trivalent lanthanides in the pH range 7-10.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Azoles
    - Subclass Imidazoles
      - Level5 Substituted imidazoles
        Level6 Carbonylimidazoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Azoles
Subclass	Imidazoles
Intermediate Tree Nodes	Substituted imidazoles
Direct Parent	Carbonylimidazoles
Alternative Parents	Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Imidazole-4-carbonyl group - Heteroaromatic compound - Azacycle - Monocarboxylic acid or derivatives - 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 carbonylimidazoles. These are substituted imidazoles in which the imidazole ring bears a carbonyl group.
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

Associated Targets(Human)

SLC6A1 Tclin GABA transporter 1 (308 Activities)

Discover Target: SLC6A1

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

SLC6A11 Tchem GABA transporter 3 (176 Activities)

Discover Target: SLC6A11

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	504752520
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752520
IUPAC Name	1H-imidazole-5-carboxylic acid
INCHI	InChI=1S/C4H4N2O2/c7-4(8)3-1-5-2-6-3/h1-2H,(H,5,6)(H,7,8)
InChIKey	NKWCGTOZTHZDHB-UHFFFAOYSA-N
Smiles	C1=C(NC=N1)C(=O)O
Isomeric SMILES	C1=C(NC=N1)C(=O)O
WGK Germany	3
RTECS	NI4001000
Molecular Weight	112.09
Beilstein	25(3/4)720
Reaxy-Rn	2626
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2626&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.

16 results found

Lot Number	Certificate Type	Date	Item
D2101044	Certificate of Analysis	Jan 09, 2025	I111403
F2421543	Certificate of Analysis	Jun 05, 2024	I111403
F2421550	Certificate of Analysis	Jun 05, 2024	I111403
F2421544	Certificate of Analysis	Jun 05, 2024	I111403
F2421549	Certificate of Analysis	Jun 05, 2024	I111403
F2421480	Certificate of Analysis	Jun 05, 2024	I111403
F2421542	Certificate of Analysis	Jun 05, 2024	I111403
G1223067	Certificate of Analysis	Mar 14, 2024	I111403
B2303349	Certificate of Analysis	Oct 26, 2022	I111403
G2304021	Certificate of Analysis	Oct 26, 2022	I111403
B2303354	Certificate of Analysis	Oct 26, 2022	I111403
B2303356	Certificate of Analysis	Oct 26, 2022	I111403
B2303353	Certificate of Analysis	Oct 26, 2022	I111403
B2303351	Certificate of Analysis	Oct 26, 2022	I111403
B2303423	Certificate of Analysis	Oct 26, 2022	I111403
H1807101	Certificate of Analysis	Jun 15, 2022	I111403

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Chemical and Physical Properties

Sensitivity	heat sensitive
Melt Point(°C)	294-295°C
Molecular Weight	112.090 g/mol
XLogP3	-0.100
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	112.027 Da
Monoisotopic Mass	112.027 Da
Topological Polar Surface Area	66.000 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	104.000
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

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yifei Ma, Lijie Zhang, Hong Yang, Shanshan Zhu, Jinhua Liu. (2025) Imidazole-triggered in situ fluorescence reaction system for quantitatively determination of dopamine from multiple sources. TALANTA, (127975).

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