Organic iodide salts

Sigma Aldrich N,N-Dimethylmethyleneiminium iodide

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

Sigma Aldrich 2-Chloro-1-methylpyridinium iodide

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

Sigma Aldrich 2-Acetamidophenol

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

Sigma Aldrich Trimethylsulfoxonium iodide

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

Pfaltz & Bauer 1,1-DIMETHYL-4-PHENYLPIP 5G

1,1-Dimethyl-4-phenylpiperazin 5G CAS# 54-77-3

Medchemexpress LLC J-113863 | 353791-85-2 | MFCD09971097 | ≥99.0% | 655.44 | C30H37Cl2IN2O2 | 5 MG

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J-113863 is a small-molecule chemokine receptor antagonist selective for CCR1, with demonstrated activity against human CCR3. Supplied as a solid research reagent (CAS 353791-85-2), it is intended for in vitro and preclinical receptor pharmacology studies.

• Potent CCR1 antagonist activity (human IC50 0.9 nM).
• Also active at human CCR3 (IC50 0.58 nM).
• Provided as small solid quantities suitable for biochemical and cell-based assays.
• Supplied with COA and SDS for lot-specific quality and handling information.
• Storage recommendations available for solid and solution formats to preserve stability.

Medchemexpress LLC J-113863 | 353791-85-2 | MFCD09971097 | ≥99.0% | 655.44 g/mol | C30H37Cl2IN2O2 | 100 MG

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Small and/or specialty supplier based on Federal laws and SBA requirements.
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J-113863 is a potent, selective small-molecule antagonist of C-C chemokine receptor 1 (CCR1) used in research on chemokine signaling and inflammation (CAS 353791-85-2). It exhibits sub-nanomolar to low-nanomolar activity versus CCR1 and potent activity versus human CCR3.

• Potent CCR1 antagonist; human CCR1 IC50 = 0.9 nM, mouse CCR1 IC50 = 5.8 nM.
• Potent human CCR3 antagonist (IC50 = 0.58 nM).
• Available as solid powder and as a DMSO solution; multiple pack sizes including 100 mg.
• High purity (≥99.0%) suitable for in vitro pharmacology.
• Used in chemokine receptor and inflammation research applications.

Medchemexpress LLC Piperidinium, 1-(1-cycloocten-1-ylmethyl)-4-[(2,7-dichloro-9H-xanthen-9-yl)carbonyl]amino iodide | 353791-85-2 | MFCD09971097 | 95.2% | 655.44 g/mol | C30H37Cl2IN2O2 | 50 MG

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Small and/or specialty supplier based on Federal laws and SBA requirements.
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J-113863 is a small-molecule CCR1 receptor antagonist provided for research use. It is supplied as solid material and as DMSO solutions and is used in vitro to study chemokine receptor signaling and receptor antagonism.

• Potent CCR1 antagonist (human IC50 0.9 nM; mouse IC50 5.8 nM).
• Also a potent human CCR3 antagonist (IC50 0.58 nM).
• Available as solid and 10 mM DMSO solutions for ready-to-use assays.
• Molecular weight 655.44 g/mol; formula C30H37Cl2IN2O2; CAS 353791-85-2.
• Typical purity reported 95.19% (data sheet); batch-specific certificate of analysis available.
• Intended for in vitro pharmacology and receptor signaling research only.

Medchemexpress LLC Piperidinium, 1-(1-cycloocten-1-ylmethyl)-4-[[(2,7-dichloro-9H-xanthen-9-yl)carbonyl]amino]-1-ethyl | 353791-85-2 | 95.2% | 655.44 g·mol⁻¹ | C30H37Cl2IN2O2 | 10 MG

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Small and/or specialty supplier based on Federal laws and SBA requirements.
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A potent, selective small-molecule antagonist of chemokine receptors CCR1 and CCR3 used for receptor pharmacology and anti-inflammatory research.

• Potent CCR1 antagonist: human IC50 0.9 nM; mouse IC50 5.8 nM.
• Potent human CCR3 antagonist (IC50 0.58 nM); weak mouse CCR3 activity (IC50 460 nM).
• Purity 95.2%.
• Molecular weight 655.44 g·mol⁻¹; chemical formula C30H37Cl2IN2O2.
• CAS 353791-85-2.
• Available as solid (mg quantities) and as 10 mM solution in DMSO.
• Storage: solid at 4°C; in solvent -80°C (up to 6 months) or -20°C (up to 1 month).