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Levobunolol hydrochloride

Levobunolol hydrochloride Suppliers list
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
Email: sales@conier.com
Products Intro: Product Name:levobunolol hydrochloride
CAS:27912-14-7
Purity:99% Package:1kg
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-29-87569265 +86-18612256290
Email: 1056@dideu.com
Products Intro: Product Name:Levobunolol hydrochloride
CAS:27912-14-7
Purity:99% Package:1g;1USD|10g;1USD|100g;1USD|1KG;1USD|25KG;1USD
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Products Intro: Product Name:Levobunolol hydrochloride;l-Bunolol hydrochloride
CAS:27912-14-7
Purity:98.00% Package:10 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-029-89586680 +86-18192503167
Email: 1026@dideu.com
Products Intro: Product Name:Levobunolol hydrochloride USP/EP/BP
CAS:27912-14-7
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer
Company Name: Dideu Industries Group Limited
Tel: +86-29-89586680 +86-15129568250
Email: 1026@dideu.com
Products Intro: Product Name:Levobunolol hydrochloride
CAS:27912-14-7
Purity:99.9% Package:1g;1.1USD Remarks:FDA GMP CEP Approved Manufacturer

Levobunolol hydrochloride manufacturers

Levobunolol hydrochloride Basic information
Product Name:Levobunolol hydrochloride
Synonyms:(-)-5-[3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydronaphthalene-1(2H)-one hydrochloride;5-[3-(tert-Butylamino)-2-hydroxypropoxy]-3,4-dihydro-2H-naphthalen-1-one hydrochloride;AG-901;Levobunolol Hydrochloride (200 mg)H0E0470.999mg/mg(dr);Levobunolol Hydrochloride (200 mg);(-)-3,4-dihydro-5-(3-(tert-butylamino)-2-hydroxypropoxy)-1(2h)-naphthalenone;LEVOBUNOLOL HCL;LEVOBUNOLOL HYDROCHLORIDE
CAS:27912-14-7
MF:C17H26ClNO3
MW:327.85
EINECS:248-725-3
Product Categories:API
Mol File:27912-14-7.mol
Levobunolol hydrochloride Structure
Levobunolol hydrochloride Chemical Properties
Melting point 209-211°
alpha 24589 -19.6±0.7° (c = 2.90 in methanol)
storage temp. Amber Vial, Refrigerator, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly), Water (Sparingly)
form Solid
color White to Off-White
Stability:Light Sensitive
Safety Information
HS Code 2922504500
MSDS Information
Levobunolol hydrochloride Usage And Synthesis
DescriptionLevobunolol hydrochloride is a non-selective β-adrenergic blocker useful in the treatment of glaucoma. Worldwide, it represents the sixth B-blocker to be launched for this indication.
OriginatorWarner Lambert (USA)
UsesAnti-adrenergic (β-receptor).
UsesA non-selective ?-adrenoceptor antagonist used as an anticonvulsant.
DefinitionChEBI: A hydrochloride obtained by combining equimolar amounts of levobunolol and hydrochloric acid. A non-selective beta-adrenergic antagonist used for treatment of glaucoma.
Manufacturing Process9.62 g (59 mmoles) 5-hydroxy-3,4-dihydro-1(2H)-naphthalenone, 67 ml toluene, 0.36 g (1.1 mmoles) tetra-n-butylammonium bromide, 4.51 g (68 mmoles) 85% potassium hydroxide and 20 ml (254 mmoles) (R)-(-)- epichlorhydrine were placed in an appropriate flask fitted with efficient mechanical stirring, and the mixture was heated under reflux for two hours. The mixture was allowed to cool to 30°C, 50 ml toluene and 50 ml water were added and the mixture was vigorously stirred. The organic phase was removed and the aqueous phase extracted with 25 ml toluene. The combined organic phases were concentrated at reduced pressure, 31 ml (300 mmoles) tert-butylamine, 45 ml ethanol and 3 ml deionized water were added, and the solution was heated under reflux for one hour. The mixture was allowed to cool to 40°C and the volatile products were distilled at reduced pressure. Toluene (9 ml) was added to the residue and volatiles were distilled at reduced pressure. (S)-5-(2,3-Epoxypropoxy)-3,4-dihydro-1(2H)- naphthalenone with an optical purity greater than 95% was obtained. Toluene (75 ml) was added to the product, and then, 10 ml of 35% (w/v) hydrochloric acid and 110 ml water, and the mixture was stirred for fifteen minutes. The organic phase was decanted and the aqueous one was extracted with 50 ml toluene. The aqueous phase was basified by addition of a solution of 5.1 g sodium hydroxide in 150 ml water and extracted twice with toluene (100 and 50 ml, respectively). The combined organic extracts were dried with anhydrous sodium sulfate, decolorized with active charcoal and filtered.
To the above toluenic solution containing levobunolol as free base, 16 ml ethanol and the stoichiometric amount of hydrogen chloride were added. The stirred mixture was cooled below 10°C and kept at this temperature for one hour. The precipitated solid was filtered, washed with toluene, recrystallized twice from 43 ml ethanol and dried to give 10.0 g (51% yield) of (-)-3,4- dihydro-5-(3-(tert-butylamino)-2-hydroxypropoxy)-1(2H)-naphthalenone hydrochloride (levobunolol hydrochloride) having a rotary power at 25°C below -19°.
Brand nameAkbeta(Akorn); Betagan(Allergan);VISTAGEN LIQUIFILM.
Therapeutic FunctionBeta-adrenergic blocker
Veterinary Drugs and TreatmentsLevobunolol HCl is a beta1- and beta2-blocking agent similar to timolol and metipranolol above but without the potential for myocardial depression or airway constriction noted rarely in veterinary medicine and occasionally in human patients. Levobunolol is used in humans with glaucoma responsive to beta adrenergic blocking agents but who suffer cardiac and respiratory side effects associated with timolol. Levobunolol HCl and then carteolol HCl would be suitable Beta blocking agents for feline patients with glaucoma and asthma, although carbonic anhydrase inhibitors should be used in such cases prior to adding a Beta blocking agent.
Levobunolol hydrochloride Preparation Products And Raw materials
Raw materialstert-Butylamine-->4-(3,4-Dichlorophenyl)-1-tetralone-->Tetrabutylammonium bromide-->Potassium hydroxide-->1-Tetralone
Tag:Levobunolol hydrochloride(27912-14-7) Related Product Information
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