Imidazole - Suitable for molecular biology, ≥99%(T) , CAS No.288-32-4

CAS: 288-32-4 Cat. No.: I485681 Fórmula: C3H4N2 Peso molecular: 68.08 Beilstein Registry Number: 103853 Número EC: 206-019-2
Disponible para pedir
GRADE & PURITY Suitable for molecular biology ? Molecular-biology grade — free of nucleases and contaminants that degrade DNA/RNA. Use in cloning, PCR, and nucleic-acid work needing clean reagents. ≥99%(T)
Synonyms
CHEBI:14434 | 1H-Imidazole | BRN 0103853 | SILDENAFIL CITRATE IMPURITY E [EP IMPURITY] | BDBM7882 | I0001 | Imidazole, ReagentPlus(R), 99% | FLUTRIMAZOLE IMPURITY A [EP IMPURITY] | Formamidine,N'-vinylene- | Glyoxaline solution | Him | NSC-60522 | UNII-7G
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
USA
Alemania (EU)*
Price
Qty
5g
I485681-5g
2 Disponible
—
11,90US$
25g
I485681-25g
1 Disponible
—
17,90US$
100g
I485681-100g
2 Disponible
—
20,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Suitable for molecular biology, ≥99%(T) Suitable for molecular biology for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 429 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) proteinin elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatographyas a component of homogenization buffer for the purification of phagosomal compartments from dendritic cellsExcellent for buffers in the range of pH 6.2-7.8

General description

Imidazole, also known as ethoxyquin, is an aromatic heterocyclic diazole and a key biological buffer with a pH range of 6.2 to 7.8 at 25°C. It has a wide range of applications in molecular biology, biochemistry, proteomics, and other fields. In proteomics, imidazole is crucial for eluting histidine-tagged proteins from IMAC columns. It is a strong chelator of divalent cations, such as nickel and zinc, disrupting the interaction between the His tag and the metal ions, allowing for efficient elution of purified proteins.
Imidazole is also essential for improving protein purity. It is widely used in preparing buffer solutions for downstream cleanup column optimization. Imidazole solutions are also effective eluents and cleaning agents throughout the protein purification process. Furthermore, imidazole can be used in horseradish peroxidase (HRP) assays and reverse staining of SDS-PAGE gels for protein detection. Imidazole is a valuable biological reagent with a wide range of applications. It is a key component of many buffers and is also used in protein purification and detection protocols.

Specifications

Sinónimos
CHEBI:14434 | 1H-Imidazole | BRN 0103853 | SILDENAFIL CITRATE IMPURITY E [EP IMPURITY] | BDBM7882 | I0001 | Imidazole, ReagentPlus(R), 99% | FLUTRIMAZOLE IMPURITY A [EP IMPURITY] | Formamidine,N'-vinylene- | Glyoxaline solution | Him | NSC-60522 | UNII-7G
Especificaciones y pureza
Suitable for molecular biology, ≥99%(T)
Mecanismos bioquímicos y fisiológicos
Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 F
Condiciones de almacenamiento de almacenamiento
Room temperature,Argon charged
Enviado en
Normal
Grado
Suitable for molecular biology
Pureza
≥99%(T)
Nombres e identificadores
Pubchem Sid528770852
Sonrisas canónicasC1=CN=CN1
IUPAC Name1H-imidazole
InChIKeyRAXXELZNTBOGNW-UHFFFAOYSA-N
INCHI1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
Isómeros SMILES C1=CN=CN1
WGK Alemania 1
RTECS NI3325000
Número ONU 2923
Peso molecular 68.08
Beilstein 103853
Reaxy-Rn 103853
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=103853&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseAzoles
SubclassImidazoles
Intermediate Tree Nodes Not available
Direct ParentImidazoles
Alternative Parents Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Heteroaromatic compound - Imidazole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as imidazoles. These are compounds containing an imidazole ring, which is an aromatic five-member ring with two nitrogen atoms at positions 1 and 3, and three carbon atoms.
External Descriptors an aromatic compound
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
EPHX1 Tchem Epoxide hydrolase 1 (644 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXAS1 Tchem Thromboxane-A synthase (3355 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGIS Tchem Prostaglandin I2 synthase (104 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SW480 (6023 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
QPCT Tchem Glutaminyl-peptide cyclotransferase (1121 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMMC-7721 (5516 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FKBP5 Tchem Peptidyl-prolyl cis-trans isomerase FKBP5 (259 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHO (4503 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
L2315095Certificate of AnalysisSep 07, 2026 I485681
L2315096Certificate of AnalysisSep 07, 2026 I485681
L2315097Certificate of AnalysisSep 07, 2026 I485681
E2609143Certificate of AnalysisMay 15, 2026 I485681
E2609148Certificate of AnalysisMay 13, 2026 I485681
I2526095Certificate of AnalysisSep 30, 2025 I485681
Propiedades químicas y físicas
Solubilidad water: 500mg/mL, clear, colorless to very faintly yellow
SensibilidadAir sensitive;Moisture sensitive
Punto de inflamación (°C)145℃
Punto de ebullición (°C)257°C
Punto de fusión (°C)90-91°C
Peso molecular68.080 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass68.0374 Da
Monoisotopic Mass68.0374 Da
Topological Polar Surface Area28.700 Ų
Heavy Atom Count5
Formal Charge0
Complexity28.100
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Molecular Biology Grade
Comparing Guanidine Hydrochloride and Urea for Inclusion-Body Solubilization
Why Did Nickel Agarose Beads Lose Their Color?
Why Did My Ni-Agarose Beads Turn Black or Brown?
How to Optimize Buffer Components for Ni-Agarose Beads
Stripping, Cleaning, and Metal Recharging Workflow for Ni²⁺–Agarose Resins
Obtaining soluble and biologically active recombinant proteins from inclusion bodies
How to Choose the Best Protein Purification Technique
His-Tagged Protein Purification
His-Tag Protein Purification: Common Troubleshooting Questions and Practical Solutions
Scientific Decision-Making for Chromatography Buffer Selection: Tris-HCl vs Phosphate Systems
OSF/ASF Dual-Channel Toolbox: Divergent Reactions of Four-Membered Ring Sulfonyl Fluorides, Condition “Knobs,” and Selection Navigation
Protein Tags Demystified: Classification, Properties, and Suitable Experimental Applications
Why Copper Develops Local Pinholes in Water Systems: The Film-Forming Protection Mechanism of Benzotriazole (BTA), Key Variables, and a Selection Guide (Tables 1–3)
Tuning Logic of Imidazole Heteroaromatic Building Blocks: How Dual Nitrogen Sites and Substitution / Salt Forms / Ring Fusion Modulate Charge, Hydrogen Bonding, and Coordination (with Tables A–E)
Invertebrate Oxygen Carrier Proteins in Immunology and Vaccine Research
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
4-[(tert-Butyldimethylsilyl)oxy]butan-1-ol: Experimental Selection Logic as a Monoprotected 1,4-Butanediol Building Block and a Protected C4 Linker
Formulation Design and Selection of Amine Curing Agents in Epoxy Systems
Protein Structure Analysis: An Experimental Path from Defining the Question to Functional Validation
Understanding Amine Curing Agents: Structure, Types, and Application Selection
Adding a Temperature-Triggered Switch to NCO: How Blocked Isocyanates Affect the Storage, Curing, and Film Performance of 1K Baking Coatings
Epoxy Phenolic Coatings: Why Are They Commonly Used for Chemical Resistance, Solvent Resistance, Heat Resistance, and Internal Metal Surface Protection?
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Why Is the meta-Fluoropyridine Motif Difficult to Make? Understanding the Synthetic Logic of Stable Enamine Building Blocks from the Risks of the Balz–Schiemann Reaction
Structural Features, Property Modulation, and Typical Applications of Triazole Compounds
Synthetic Application Logic of Triazoles and Related Compounds: Structural Introduction, Reactive Sites, and Target Molecule Construction
One-Pot Arylation of the Piperidine α-C–H Bond: From Directed Lithiation and Li→Zn Transmetalation to Negishi Coupling
Overcoming the Electronic-Effect Limitations of Nucleophilic Aromatic Substitution in Fluoroarenes: Anion Activation, Concerted Substitution, and HF Capture by t-Bu-P4
What Is “Plant Collagen”? Distinguishing Ingredient Types, Structural Differences, Production Methods, and Skincare Effects
Citations of This Product
Calculadoras de soluciones
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