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CHLORISONDAMINE DIIODIDE

Product Name
CHLORISONDAMINE DIIODIDE
CAS No.
96750-66-2
Chemical Name
CHLORISONDAMINE DIIODIDE
Synonyms
Chlorisondamine (iodide);CHLORCHLORISONDAMINE DIIODIDEISONDAMINE DIIODIDE;4,5,6,7-tetrachloro-2-methyl-2-[2-(trimethylammonium)ethyl]isoindolinium diiodide
CBNumber
CB7497364
Molecular Formula
C14Cl4H20I2N2
Formula Weight
611.94
MOL File
96750-66-2.mol
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CHLORISONDAMINE DIIODIDE Property

storage temp. 
2-8°C
solubility 
H2O: ~3.75 mg/mL
form 
solid
color 
white
Water Solubility 
Soluble to 10 mM in water
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Safety

Hazard Codes 
Xn,N
Risk Statements 
22-50
Safety Statements 
60-61
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
2
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C5366
Product name
Chlorisondamine diiodide
Purity
≥98% (HPLC), white solid
Packaging
10mg
Price
$195
Updated
2025/07/31
Sigma-Aldrich
Product number
C5366
Product name
Chlorisondamine diiodide
Purity
≥98% (HPLC), white solid
Packaging
50mg
Price
$734
Updated
2025/07/31
Cayman Chemical
Product number
20119
Product name
Chlorisondamine (iodide)
Purity
≥98%
Packaging
1mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
20119
Product name
Chlorisondamine (iodide)
Purity
≥98%
Packaging
5mg
Price
$108
Updated
2024/03/01
Cayman Chemical
Product number
20119
Product name
Chlorisondamine (iodide)
Purity
≥98%
Packaging
10mg
Price
$161
Updated
2024/03/01
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CHLORISONDAMINE DIIODIDE Chemical Properties,Usage,Production

Description

Chlorisondamine is an antagonist of nicotinic acetylcholine receptors (nAChRs; IC50 = 1.8 μM in rat striatal synaptosomes) and a ganglion blocker. It decreases dopamine release induced by nicotine (Item Nos. 16535 | 20887) in a dose-dependent manner in rat striatal synaptosomes at concentrations ranging from 0-100 μM. The effect of chlorisondamine is long-lasting, with a 10 mg/kg dose blocking nicotine-induced stimulant activity for at least five weeks. Chlorisondamine (5 μg, i.c.v.) prevents rats from acquiring a (–)-nicotine-induced conditioned taste aversion response, a model of the aversive effects of nicotine. It also inhibits autonomic ganglia, providing approximately 50% inhibition of the contractile response in feline superior cervical ganglion nictitating membrane preparations when administered at a dose of 50 mg/kg.

Uses

Chlorisondamine diiodide has been used:

  • as a nicotinic receptor antagonist to test its effect on trinitrobenzene sulfonic acid (TNBS)-induced colitis
  • as an irreversible nicotinic acetylcholine(nAChR) blocker to pre-treat brain samples to test its effect on cytochrome P450 2B (CYP2B) induction
  • as a ganglionic blocker to test its effect on regulating corticosterone levels in rat with chronic stress

Biochem/physiol Actions

Chlorisondamine diiodide mediates ganglionic and central blockade.

in vivo

Chlorisondamine (0.2, 1.0, 5.0 μg; IV; single dosage) antagonizes the depressant action of nicotine on vertical activity (0-20min) in a dose-dependent way at 1 and 2 weeks[1].

Animal Model:Rats (treated once with nicotine 0.4 mg/kg, s.c.)[1]
Dosage:0.2, 1.0, 5.0 μg
Administration:IV; single dosage
Result:Antagonized the depressant action of nicotine on vertical activity (0-20min) in a dose-dependent way at 1 and 2 weeks.

References

[1] H. EL-BIZRI  P. B S C. Blockade of nicotinic receptor-mediated release of dopamine from striatal synaptosomes by chlorisondamine and other nicotinic antagonists administered in vitro[J]. British Journal of Pharmacology, 1994, 111 2: 406-413. DOI: 10.1111/j.1476-5381.1994.tb14749.x
[2] CLARKE P B. Chronic central nicotinic blockade after a single administration of the bisquaternary ganglion-blocking drug chlorisondamine.[J]. British Journal of Pharmacology, 1984, 83 2: 527-535. DOI: 10.1111/j.1476-5381.1984.tb16517.x
[3] C. REAVILL. Chlorisondamine blocks acquisition of the conditioned taste aversion produced by (?)-nicotine[J]. Neuropharmacology, 1986, 25 9: Pages 1067-1069. DOI: 10.1016/0028-3908(86)90204-2
[4] A J PLUMMER. Ganglionic blockade by a new bisquaternary series, including chlorisondamine dimethochloride.[J]. Journal of Pharmacology and Experimental Therapeutics, 1955, 115 2: 172-184.

CHLORISONDAMINE DIIODIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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CHLORISONDAMINE DIIODIDE Suppliers

BOC Sciences
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1-631-485-4226; 16314854226
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United States
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Sigma-Aldrich
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021-61415566 800-8193336
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Angel Pharmatech, Ltd.
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17317130613
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QQ3358272972
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TargetMol Chemicals Inc.
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+1-781-999-5354; +17819995354
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marketing@targetmol.com
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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QQ 3610331285
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sales@chemegen.com
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MedBioPharmaceutical Technology Inc
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Energy Chemical
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TargetMol Chemicals Inc.
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marketing@tsbiochem.com
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Shanghai Tachizaki Biomedical Research Center
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sales@chemlab-tachizaki.com
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96750-66-2, CHLORISONDAMINE DIIODIDERelated Search:


  • 4,5,6,7-tetrachloro-2-methyl-2-[2-(trimethylammonium)ethyl]isoindolinium diiodide
  • Chlorisondamine (iodide)
  • CHLORCHLORISONDAMINE DIIODIDEISONDAMINE DIIODIDE
  • 96750-66-2
  • C14H20Cl4N22I