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Levamisole hydrochloride

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CAS:16595-80-5
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Levamisole hydrochloride manufacturers

  • Levamisole Hydrochloride
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  • 2024-04-25
  • CAS:16595-80-5
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Levamisole hydrochloride Basic information
Product Name:Levamisole hydrochloride
Synonyms:1-b)thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,(s)-imidazo(;1-b)thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,l-(-)-imidazo(;1-b]thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,(S)-Imidazo[2;decaris;Imidazo[2,1-b]thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,(S)-;kw-2-le-t;L-2,3,5,6-Tetrahydro-6-phenylimidazo-[2,1-6]-thiazole;levomysolhydrochloride
CAS:16595-80-5
MF:C11H13ClN2S
MW:240.75
EINECS:240-654-6
Product Categories:Other APIs;REZIFILM;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Pharma;Pharmaceutical intermediate;Antibiotic Explorer;Veterinaries;Protein Phosphatase;Asymmetric Synthesis;Synthetic Organic Chemistry;API;16595-80-5
Mol File:16595-80-5.mol
Levamisole hydrochloride Structure
Levamisole hydrochloride Chemical Properties
Melting point 266-267 °C(lit.)
alpha -128 º (c=5, H2O)
refractive index -126 ° (C=1, H2O)
Fp 9℃
storage temp. 2-8°C
solubility Freely soluble in water, soluble in ethanol (96 per cent), slightly soluble in methylene chloride.
form Crystalline Powder
color White to almost white
Water Solubility 210 g/L (20 ºC)
Merck 14,5459
BRN 4358988
BCS Class3/1
Stability:Hygroscopic
InChIInChI=1/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H/t10-;/s3
InChIKeyLAZPBGZRMVRFKY-HNCPQSOCSA-N
SMILES[C@H]1(N=C2SCCN2C1)C1=CC=CC=C1.Cl |&1:0,r|
LogP1.845 (est)
CAS DataBase Reference16595-80-5(CAS DataBase Reference)
EPA Substance Registry SystemLevamisole hydrochloride (16595-80-5)
Safety Information
Hazard Codes T,Xn,F
Risk Statements 25-20/21/22-39/23/24/25-23/24/25-11
Safety Statements 36/37/39-45-28A-36-36/37-16
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS NJ5960000
10
HazardClass 6.1(b)
PackingGroup III
HS Code 29349990
MSDS Information
Levamisole hydrochloride Usage And Synthesis
Chemical PropertiesWhite to light yellow crystalline powder, odorless, bitter taste. Melting point 227-229℃. Soluble in water, methanol, ethanol and glycerol, slightly soluble in chloroform and aether; insoluble in acetone. Stable under acidic conditions, but easy to decompose and fail under alkaline conditions.
OriginatorSolaskil,Specia,France,1971
UsesLevamisole hydrochloride is an anthelmintic. The activity of levamisole is about twice as high as that of abscisicidal, and the toxicity and side effects are lower. Levamisole can cause muscle paralysis of roundworms and then excrete them in the feces. It is mainly used as an anti-worm and anti-hookworm.
UsesBiological response modifier with anthelmintic activity. Anthelmintic (nematodes); immunomodulator.
DefinitionChEBI: Levamisole hydrochloride is an organic molecular entity.
PreparationLevamisole hydrochloride was prepared from racemic tetraimidazole by splitting, alkali analysis and acidification into salt.
Dibenzoyl-D-tartaric acid is boiled in water for 40min, hydrolyzed and neutralized with sodium hydroxide solution to pH 7.5, and then added to racemic tetraimidazole. The levamisole is precipitated by generating salt with bisbenzoyl-tartaric acid. After separation, add sodium hydroxide solution to PH=9 and decompose levamisole. Then dissolved in dilute hydrochloric acid solution, after decolorization by activated carbon, the filtrate was concentrated nearly dry, and crystallized by adding acetone and cooling to 0℃. Filtered and dried to obtain levamisole hydrochloride.
Brand nameErgamisol (Janssen);Vermisol.
Therapeutic FunctionAntiinflammatory
Biochem/physiol ActionsShows both immunostimulant and immunosuppressant effects, depending on several controllable factors. Very effective in treatment of ascariasis (hookworm infestation). Useful in chemotherapy of colorectal cancers, possibly due to its stimulation of IL-1 production and direct activation of macrophages.
PharmacologyLevamisole Hydrochloride is the hydrochloride salt of the synthetic imidazothiazole derivative levamisole with anthelminthic and immunomodulating activities. In immunosuppressed states, levamisole may restore immune function by: 1) stimulating antibody formation, 2) stimulating T-cell activation and proliferation, 3) potentiating monocyte and macrophage phagocytosis and chemotaxis and 4) increasing neutrophil mobility, adherence, and chemotaxis.
PharmacokineticsLevamisole is rapidly absorbed from all routes of administration, with peak blood levels occurring within an hour followed by rapid metabolism and depletion principally via urinary excretion, with an elimination half-life of approximately 4 h.
Mode of actionLevamisole is a cholinergic receptor agonist and elicits spastic muscle paralysis due to prolonged activation of the excitatory nicotinic acetylcholine receptors (nAChR) on nematode body wall muscle.
Toxicity evaluationSymptoms of levamisole toxicity mimic organophosphate toxicity (salivation, lacrimation, urination and defecation, hyperesthesia, seizures and irritability). There is no antidote for levamisole toxicity.
The World Health Organization reviewed hematological studies in animals and humans and derived acceptable daily intake for levamisole as 0.006 mg/kg body weight. This suggests a person can ingest 0.36 mg of levamisole/day over a lifetime without any appreciable risk.
levamisole
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