1072-84-0,MFCD01365907
Catalog No.:AA0032P2

1072-84-0 | 1H-Imidazole-5-carboxylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$12.00   $8.00
- +
10g
97%
in stock  
$17.00   $12.00
- +
25g
97%
in stock  
$40.00   $28.00
- +
100g
97%
in stock  
$152.00   $106.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032P2
Chemical Name:
1H-Imidazole-5-carboxylic acid
CAS Number:
1072-84-0
Molecular Formula:
C4H4N2O2
Molecular Weight:
112.0868
MDL Number:
MFCD01365907
SMILES:
OC(=O)c1c[nH]cn1
NSC Number:
32340
Properties
Properties
 
BP:
495°C at 760 mmHg  
Form:
Solid  
MP:
243-245 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
104  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.1  

Synonyms
 
  
Literature

Title: Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κ(2)N(3),O)cobalt(II).

Journal: Acta crystallographica. Section E, Structure reports online 20121001

Title: A new two-dimensional cadmium coordination polymer with 1H-imidazole-4-carboxylate and oxalate.

Journal: Acta crystallographica. Section C, Crystal structure communications 20120701

Title: 1H-Imidazol-3-ium-4-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20120101

Title: Cytotoxic and antimicrobial activities of Cu(II), Co(II), Pt(II) and Zn(II) Complexes with N,O-chelating heterocyclic carboxylates.

Journal: Archiv der Pharmazie 20110901

Title: catena-Poly[copper(I)-bis-[μ-3-(1H-imidazol-2-yl)pyridine]-copper(I)-di-μ-iodido].

Journal: Acta crystallographica. Section E, Structure reports online 20110901

Title: trans-Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κN,O)nickel(II).

Journal: Acta crystallographica. Section E, Structure reports online 20110701

Title: Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κN,O)zinc.

Journal: Acta crystallographica. Section E, Structure reports online 20110701

Title: Development of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors.

Journal: European journal of medicinal chemistry 20110501

Title: Trifunctional 99mTc based radiopharmaceuticals: metal-mediated conjugation of a peptide with a nucleus targeting intercalator.

Journal: Organic & biomolecular chemistry 20110221

Title: Postelicitation model of allergic contact dermatitis for predicting the efficacy of topical drugs.

Journal: Experimental dermatology 20090101

Title: Organic-inorganic hybrid materials constructed from inorganic lanthanide sulfate skeletons and organic 4,5-imidazoledicarboxylic acid.

Journal: Dalton transactions (Cambridge, England : 2003) 20070914

Title: Hair analysis of histamine and several metabolites in C3H/HeNCrj mice by ultra performance liquid chromatography with electrospray ionization time-of-flight mass spectrometry (UPLC-ESI-TOF-MS): influence of hair cycle and age.

Journal: Clinica chimica acta; international journal of clinical chemistry 20070301

Title: Phosphate ester hydrolysis by hydroxo complexes of trivalent lanthanides stabilized by 4-imidazolecarboxylate.

Journal: Inorganic chemistry 20061113

Title: Rapid determination of histamine and its metabolites in mice hair by ultra-performance liquid chromatography with time-of-flight mass spectrometry.

Journal: Journal of chromatography. A 20061103

Title: Two novel luminescent lanthanide sulfate-carboxylates with an unusual 2-D bamboo-raft-like structure based on the linkages of left- and right-handed helical tubes involving in situ decarboxylation.

Journal: Chemical communications (Cambridge, England) 20060514

Title: Synthesis and antiplatelet activity of new imidazole-4-carboxylic acid derivatives.

Journal: Archiv der Pharmazie 20051101

Title: A new [2 + 1] mixed ligand concept based on [99(m)Tc(OH2)3(CO)3]+: a basic study.

Journal: Dalton transactions (Cambridge, England : 2003) 20040507

Title: Diastereoselective formation of metallamacrocyclic (arene)Ru(II) and CpRh(III) complexes.

Journal: Inorganic chemistry 20040308

Title: Suppression of different phases of systemic contact hypersensitivity by urocanic acid oxidation products.

Journal: Photochemistry and photobiology 20040101

Application
4-Imidazolecarboxylic acid (ICA) is a compound utilized in various synthetic processes and analytical techniques. It serves as a precursor in the synthesis of triphenylmethyl-protected 4-imidazole carboxylic acid (trityl-ImCOOH), facilitating functionalization of poly(propylene imine) dendrimers. Additionally, ICA is involved in the preparation of lanthanide sulfate–carboxylates and tetranuclear manganese carboxylate complexes. Moreover, it functions as an internal standard in analytical methods, enabling calibration curve generation for histamine and metabolites isolated from mice hair. Overall, ICA plays a significant role in organic synthesis, coordination chemistry, and analytical chemistry applications.
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SDS
Tags:1072-84-0 Molecular Formula|1072-84-0 MDL|1072-84-0 SMILES|1072-84-0 1H-Imidazole-5-carboxylic acid
Catalog No.: AA0032P2
1072-84-0,MFCD01365907
1072-84-0 | 1H-Imidazole-5-carboxylic acid
Pack Size: 1g
Purity: 97%
in stock
$7.00 $5.00
Pack Size: 5g
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 10g
Purity: 97%
in stock
$17.00 $12.00
Pack Size: 25g
Purity: 97%
in stock
$40.00 $28.00
Pack Size: 100g
Purity: 97%
in stock
$152.00 $106.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0032P2
Chemical Name: 1H-Imidazole-5-carboxylic acid
CAS Number: 1072-84-0
Molecular Formula: C4H4N2O2
Molecular Weight: 112.0868
MDL Number: MFCD01365907
SMILES: OC(=O)c1c[nH]cn1
NSC Number: 32340
Properties
BP: 495°C at 760 mmHg  
Form: Solid  
MP: 243-245 °C  
Storage: Keep in dry area;Room Temperature;  
Complexity: 104  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.1  
111:   
Literature fold

Title: Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κ(2)N(3),O)cobalt(II).

Journal: Acta crystallographica. Section E, Structure reports online20121001

Title: A new two-dimensional cadmium coordination polymer with 1H-imidazole-4-carboxylate and oxalate.

Journal: Acta crystallographica. Section C, Crystal structure communications20120701

Title: 1H-Imidazol-3-ium-4-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online20120101

Title: Cytotoxic and antimicrobial activities of Cu(II), Co(II), Pt(II) and Zn(II) Complexes with N,O-chelating heterocyclic carboxylates.

Journal: Archiv der Pharmazie20110901

Title: catena-Poly[copper(I)-bis-[μ-3-(1H-imidazol-2-yl)pyridine]-copper(I)-di-μ-iodido].

Journal: Acta crystallographica. Section E, Structure reports online20110901

Title: trans-Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κN,O)nickel(II).

Journal: Acta crystallographica. Section E, Structure reports online20110701

Title: Diaqua-bis-(1H-imidazole-4-carboxyl-ato-κN,O)zinc.

Journal: Acta crystallographica. Section E, Structure reports online20110701

Title: Development of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors.

Journal: European journal of medicinal chemistry20110501

Title: Trifunctional 99mTc based radiopharmaceuticals: metal-mediated conjugation of a peptide with a nucleus targeting intercalator.

Journal: Organic & biomolecular chemistry20110221

Title: Postelicitation model of allergic contact dermatitis for predicting the efficacy of topical drugs.

Journal: Experimental dermatology20090101

Title: Organic-inorganic hybrid materials constructed from inorganic lanthanide sulfate skeletons and organic 4,5-imidazoledicarboxylic acid.

Journal: Dalton transactions (Cambridge, England : 2003)20070914

Title: Hair analysis of histamine and several metabolites in C3H/HeNCrj mice by ultra performance liquid chromatography with electrospray ionization time-of-flight mass spectrometry (UPLC-ESI-TOF-MS): influence of hair cycle and age.

Journal: Clinica chimica acta; international journal of clinical chemistry20070301

Title: Phosphate ester hydrolysis by hydroxo complexes of trivalent lanthanides stabilized by 4-imidazolecarboxylate.

Journal: Inorganic chemistry20061113

Title: Rapid determination of histamine and its metabolites in mice hair by ultra-performance liquid chromatography with time-of-flight mass spectrometry.

Journal: Journal of chromatography. A20061103

Title: Two novel luminescent lanthanide sulfate-carboxylates with an unusual 2-D bamboo-raft-like structure based on the linkages of left- and right-handed helical tubes involving in situ decarboxylation.

Journal: Chemical communications (Cambridge, England)20060514

Title: Synthesis and antiplatelet activity of new imidazole-4-carboxylic acid derivatives.

Journal: Archiv der Pharmazie20051101

Title: A new [2 + 1] mixed ligand concept based on [99(m)Tc(OH2)3(CO)3]+: a basic study.

Journal: Dalton transactions (Cambridge, England : 2003)20040507

Title: Diastereoselective formation of metallamacrocyclic (arene)Ru(II) and CpRh(III) complexes.

Journal: Inorganic chemistry20040308

Title: Suppression of different phases of systemic contact hypersensitivity by urocanic acid oxidation products.

Journal: Photochemistry and photobiology20040101

Application fold
4-Imidazolecarboxylic acid (ICA) is a compound utilized in various synthetic processes and analytical techniques. It serves as a precursor in the synthesis of triphenylmethyl-protected 4-imidazole carboxylic acid (trityl-ImCOOH), facilitating functionalization of poly(propylene imine) dendrimers. Additionally, ICA is involved in the preparation of lanthanide sulfate–carboxylates and tetranuclear manganese carboxylate complexes. Moreover, it functions as an internal standard in analytical methods, enabling calibration curve generation for histamine and metabolites isolated from mice hair. Overall, ICA plays a significant role in organic synthesis, coordination chemistry, and analytical chemistry applications.
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