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CALMIDAZOLIUM CHLORIDE

CALMIDAZOLIUM CHLORIDE Structure
CALMIDAZOLIUM CHLORIDE structure
CAS No.
94724-12-6
Chemical Name:
CALMIDAZOLIUM CHLORIDE
Synonyms
Poly-p-methoxyphenethylmethylamine;R 24571;CALMIDAZOLIUM;COMPOUND 48/80;COMPOUND R24571;R 24571 CHLORIDE;CALMIDAZOLIUM CHLORIDE;CALMODULIN INHIBITOR R 24571;COMPOUND 48/80 TRIHYDROCHLORIDE;Compound 48/80 trihydrochloride, G protein activator
CBNumber:
CB7231629
Molecular Formula:
C32H45N3O3
Molecular Weight:
519.72
MDL Number:
MFCD00077679
MOL File:
94724-12-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-20 15:45:00
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CALMIDAZOLIUM CHLORIDE Properties

Boiling point 630.9±50.0 °C(Predicted)
Density 1.050±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility H2O: 50 mg/mL
pka 10.81±0.10(Predicted)
form solid
color white

SAFETY

Risk and Safety Statements

Hazard Codes  T
Risk Statements  23/24/25
Safety Statements  22-24/25-45-36/37
RIDADR  UN 2811 6.1/PG 2
WGK Germany  3
F  3-8-10

CALMIDAZOLIUM CHLORIDE price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0255613 Compound 48/80 99.98% 94724-12-6 5mg $39 2026-06-04 Buy
ChemScene CS-0255613 Compound 48/80 99.98% 94724-12-6 10mg $60 2026-06-04 Buy
ChemScene CS-0255613 Compound 48/80 99.98% 94724-12-6 25mg $108 2026-06-04 Buy
ChemScene CS-0255613 Compound 48/80 99.98% 94724-12-6 50mg $173 2026-06-04 Buy
ChemScene CS-0255613 Compound 48/80 99.98% 94724-12-6 100mg $298 2026-06-04 Buy
Product number Packaging Price Buy
CS-0255613 5mg $39 Buy
CS-0255613 10mg $60 Buy
CS-0255613 25mg $108 Buy
CS-0255613 50mg $173 Buy
CS-0255613 100mg $298 Buy

CALMIDAZOLIUM CHLORIDE Chemical Properties, Uses, Production

Uses

Compound 48/80 (Poly-p-methoxyphenethylmethylamine) is widely used in animal and tissue models as a "selective" mast cell activator. Compound 48/80 acts at the mast cell membrane to stimulate trimeric G-proteins and induces degranulation via phospholipase C and D pathways[1][2].

References

[1] Schemann M, et al. The mast cell degranulator compound 48/80 directly activates neurons. PLoS One. 2012;7(12):e52104. DOI:10.1371/journal.pone.0052104
[2] Wang YH, Taché Y, Harris AG, Kreutner W, Daly AF, Wei JY. Desloratadine prevents compound 48/80-induced mast cell degranulation: visualization using a vital fluorescent dye technique. Allergy. 2005;60(1):117-124. DOI:10.1111/j.1398-9995.2004.00641.x
[3] Darzynkiewicz Z, Carter S. Compound 48/80 impairs cytokinesis in murine leukemic cells. J Cell Physiol. 1984;119(1):1-6. DOI:10.1002/jcp.1041190102

CALMIDAZOLIUM CHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

CALMIDAZOLIUM CHLORIDE Suppliers

Global Suppliers ( 45)
Supplier Tel Email Country ProdList Advantage
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Shanghai Maclean Biochemical Technology Co., LTD 021-50706066 15221275939 shenlinxing@macklin.cn China 29676 58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 025-025-66113011 15955137747 cb5@aikonchem.com China 10354 58
Shanghai Aladdin Biochemical Technology Co.,Ltd. 6206333 13167063860 anhua.mao@aladdin-e.com China 43553 58
Shanghai Amole Biotechnology Co., Ltd. 13370042665 18916960931 2596183085@qq.com China 17234 58
Guangzhou Ruidi Biotechnology Co., Ltd. 020-82099279 18988941402 sales@ubiochem.com China 9998 58
Supplier Advantage
Sigma-Aldrich 80
Shanghai EFE Biological Technology Co., Ltd. 58
Shanghai YuanYe Biotechnology Co., Ltd. 60
Shanghai Maclean Biochemical Technology Co., LTD 58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 58
Shanghai Aladdin Biochemical Technology Co.,Ltd. 58
Shanghai Amole Biotechnology Co., Ltd. 58
Guangzhou Ruidi Biotechnology Co., Ltd. 58

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COMPOUND 48/80 COMPOUND 48/80 TRIHYDROCHLORIDE COMPOUND R24571 R 24571 R 24571 CHLORIDE CALMODULIN INHIBITOR R 24571 CALMIDAZOLIUM CALMIDAZOLIUM CHLORIDE 1-[Bis(4-Chlorophenyl)methyl]-3-[2-(2,4-dichlorophenyl)-2-(2,4-dichlorobenzyloxy)ethyl]-1H-imidazolium chloride 1-[BIS-(4-CHLOROPHENYL)METHYL]-3-[2-(2,4-DICHLOROPHENYL)-2-[(2,4-DICHLOROPHENYL)METHOXY]-ETHYL]-1H-IMIDAZOLIUM CHLORIDE 1-[BIS(4-CHLOROPHENYL)METHYL]-3-[2,4-DICHLORO-BETA-(2,4-DICHLOROBENZYLOXY)PHENETHYL]IMIDAZOLIUM CHLORIDE 1-[BIS(P-CHLOROPHENYL)METHYL]-3-[2-(2,4-DICHLORO-BETA-(2,4-DICHLOROBENZYLOXY)PHENETHYL)]IMIDAZOLIUM CHLORIDE 1-[BIS(P-CHLOROPHENYL)METHYL]-3-[2,4-DICHLORO-BETA-(2,4 DICHLOROBENZYLOXY) PHENETHYL]-IMIDAZOLIUM CHLORIDE [1-BIS-P-CHLOROPHENYL) METHYL]-3-[2,4-DICHLORO-BETA-(2,4-DICHLOROBENZYLOXY) PHENYL]-IMIDAZOLIUM CHLORIDE Benzeneethanamine, 4-methoxy-3,5-bis[[2-methoxy-5-[2-(methylamino)ethyl]phenyl]methyl]-N-methyl- Compound 48/80 trihydrochloride, G protein activator Poly-p-methoxyphenethylmethylamine 94724-12-6 C32H45N3O3 Cell Signaling and Neuroscience Cell Biology Calcium Antagonists BioChemical Biochemicals and Reagents Antibiotics Antibiotics A-F Antibiotics A to Z Other Intracellular Calcium Signaling Enzyme Inhibitors by Type Enzyme Inhibitors Enzymes, Inhibitors, and Substrates Antibiotics A-FEnzyme Inhibitors by Enzyme Phospholipase CLipids in Cell Signaling Phospholipase Inhibitors Antibiotics Antibiotics A to P to Phospholipid Metabolism