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1104-22-9

1104-22-9 Structure

1104-22-9 Structure
IdentificationMore
[Name]

Meclizine dihydrochloride
[CAS]

1104-22-9
[Synonyms]

1-([4-CHLOROPHENYL]PHENYLMETHYL)-4-([3-METHYLPHENYL]-METHYL)PIPERAZINE DIHYDROCHLORIDE
MECLIZINE DIHYDROCHLORIDE
1-((4-chlorophenyl)phenylmethyl)-4-((3-methylphenyl)methyl)-piperazindih
1-(p-chloro-alpha-phenylbenzyl)-4-(m-methylbenzyl)-piperazindihydrochlorid
1-[(4-chlorophenyl)phenylmethyl]-4-[(3-methylphenyl)methyl]-piperazindihyd
1-p-chlorbenzhydryl-m-methylbenzylpiperazinedihydrochloride
ancolandihydrochloride
bonamine
diadril
meclozinedihydrochloride
parachloraminedihydrochloride
Meclozine dihydrochloride monohydrate
Meclizine diHCl
1-(p-Chloro-a-phenylbenzyl)-4-(m-methylbenzyl)piperazine dihydrochloride
mecilizine hydrochloride
Navidoxine
NSC 28728
Piperazine, 1-(p-chloro-a-phenylbenzyl)-4-(m-methylbenzyl)-, dihydrochloride (6CI, 8CI)
Piperazine, 1-[(4-chlorophenyl)phenylmethyl]-4-[(3-methylphenyl)methyl]-, dihydrochloride (9CI)
Postafene dihydrochloride
[EINECS(EC#)]

214-164-8
[Molecular Formula]

C25H29Cl3N2
[MDL Number]

MFCD00058199
[Molecular Weight]

463.87
[MOL File]

1104-22-9.mol
Chemical PropertiesBack Directory
[Appearance]

White or yellowish-white, slightly hygroscopic, crystalline powder.
[Melting point ]

210.0 to 214.0 °C
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble5mg/mL, clear (warmed)
[form ]

powder
[color ]

white to beige
[CAS DataBase Reference]

1104-22-9(CAS DataBase Reference)
[EPA Substance Registry System]

1104-22-9(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R63:Possible risk of harm to the unborn child.
[Safety Statements ]

S22:Do not breathe dust .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[RTECS ]

TL2005000
[HS Code ]

2933.59.8000
[Safety Profile]

Moderately toxic by ingestion and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits very toxic fumes of Cland NOx.
[Toxicity]

LD50 oral in mouse: 1600mg/kg
Hazard InformationBack Directory
[Description]

Meclizine is a histamine H1 receptor antagonist (Ki = 250 nM). Pretreatment with meclizine (2.5-30 mg/kg, i.p.) reduces ovalbumin-induced mast cell degranulation, edema, and leukocyte influx in rat lung. Formulations containing meclizine have been used in the treatment of motion sickness and vertigo.
[Chemical Properties]

White or yellowish-white, slightly hygroscopic, crystalline powder.
[Originator]

Antivert,Roerig,US,1957
[Uses]

Antiemetic;Histamine antagonist
[Uses]

cholinergic, diagnostic aid
[Uses]

Meclizine Dihydrochloride is a histamine H1 receptor antagonist with antiemetic properties. Meclizine Dihydrochloride is a research product for neuroscience. This compound may exhibit neuroprotective properties.
[Manufacturing Process]

32.3 g of 1-p-chlorobenzhydryl-4-benzyl-piperazine, dissolved in 300 cm3 of alcohol are heated in an autoclave vessel, in the presence of Raney nickel, under a pressure of 100 kg H2, at about 150°C for 6 hours. The catalyst is filtered, the solvent is evaporated and the residue is fractionated under a high vacuum. p-Chlorobenzylhydryl-piperazine (BP 180° to 185°C/1 mm Hg) is isolated with a yield of 75%. Then finely ground NaNH2 is added. The mixture is heated under reflux for 1 hour, the mass is cooled and a molar equivalent of m-methyl benzyl chloride is added.
The solvent is evaporated and the residue is dissolved in chloroform. This solution is washed with a saturated solution of K2CO3 and dried on K2CO3. The solvent is evaporated and the residue is distilled under high vacuum. The product of the condensation distills near 230°C at 2 mm Hg pressure and the corresponding dihydrochloride melts at 217° to 224°C.
[Brand name]

Antivert (Pfizer).
[Therapeutic Function]

Antinauseant
[Biochem/physiol Actions]

Meclizine has the ability to increase glycolysis and decrease cellular ATP levels in media that has glucose and galactose. It guards the kidney against ischemia-reperfusion injury. Meclizine is considered as an anti-nausea and anti-dizziness drug, was identified in a ′nutrient-sensitized′ chemical screen. In human, it acts as an agonist of pregnane X receptor (PXR). It enhances the expression of CYP3A4 (cytochrome P450 3A4) mRNA and reduces CYP3A-catalyzed testosterone 6β-hydroxylation in primary cultures of human hepatocytes.
[Solubility in organics]

Meclizine dihydrochloride is readily soluble in chloroform and pyridine, slightly soluble in dilute acids and ethanol, and insoluble in water or ether.
[storage]

Desiccate at RT
Spectrum DetailBack Directory
[Spectrum Detail]

Meclizine dihydrochloride(1104-22-9)1HNMR
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