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CALMIDAZOLIUM CHLORIDE

Product Name
CALMIDAZOLIUM CHLORIDE
CAS No.
94724-12-6
Chemical Name
CALMIDAZOLIUM CHLORIDE
Synonyms
R 24571;CALMIDAZOLIUM;COMPOUND 48/80;COMPOUND R24571;R 24571 CHLORIDE;CALMIDAZOLIUM CHLORIDE;CALMODULIN INHIBITOR R 24571;COMPOUND 48/80 TRIHYDROCHLORIDE;Poly-p-methoxyphenethylmethylamine;Compound 48/80 trihydrochloride, G protein activator
CBNumber
CB7231629
Molecular Formula
C32H45N3O3
Formula Weight
519.72
MOL File
94724-12-6.mol
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CALMIDAZOLIUM CHLORIDE Property

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
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Safety

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
3-8-10
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Hazard and Precautionary Statements (GHS)

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CALMIDAZOLIUM CHLORIDE Chemical Properties,Usage,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

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CALMIDAZOLIUM CHLORIDE Suppliers

Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 13167063860
Fax
021-50323701
Email
anhua.mao@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51395
Advantage
80
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Shanghai Maclean Biochemical Technology Co., LTD
Tel
021-021-50706066 15221275939
Email
shenlinxing@macklin.cn
Country
China
ProdList
29784
Advantage
58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-025-66113011 18626450290
Email
cb5@aikonchem.com
Country
China
ProdList
10358
Advantage
58
Shanghai Aladdin Biochemical Technology Co.,Ltd.
Tel
400-6206333 13167063860
Email
anhua.mao@aladdin-e.com
Country
China
ProdList
48457
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58
Enzo Biochem Inc
Tel
Enzo Biochem Inc. 13797054060
Email
Enzoname@qq.com
Country
China
ProdList
6174
Advantage
58
Merck KGaA
Tel
21-20338288
Email
ordercn@merckgroup.com
Country
China
ProdList
6394
Advantage
58
Santa Cruz Biotechnology Inc
Tel
021-60936350
Email
scbt@scbt.com
Country
China
ProdList
6594
Advantage
58

94724-12-6, CALMIDAZOLIUM CHLORIDERelated Search:


  • 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-
  • Poly-p-methoxyphenethylmethylamine
  • Compound 48/80 trihydrochloride, G protein activator
  • 94724-12-6
  • C32H45N3O3
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