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Benzathine Penicillin

Benzathine Penicillin Suppliers list
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Email: bang.manoharlal@gmail.com
Products Intro: Cas:1538-09-6
ProductName:Benzathine penicillin
Purity: 98% | Package: 1 kg,5 kg, 10 kg,25kg and 1 MT
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Email: jinesh@dodhiagroup.com
Products Intro: Cas:1538-09-6
ProductName:Benzathine penicillin
Purity: 99% | Package: 1 kg,5 kg, 10 kg,25kg
Company Name: QUALITY CONTROL SOLUTIONS LTD.  
Tel: 13670046396
Email: sales@chem-strong.com
Products Intro: Cas:1538-09-6
ProductName:Benzathine penicillin
Purity: 95% HPLC | Package: 10MG;25MG;50MG;100MG
Company Name: Nantong Zhonghe Chemical New Materials Co., Ltd  
Tel: 13003551299 13003551299
Email: 2369399482@qq.com
Products Intro: Cas:1538-09-6
ProductName:Benzathine penicillin
Purity: 98.00% | Package: 1KG;25KG
Company Name: Wuhan Xiju Biotechnology Co., Ltd  
Tel: 13001802035
Email: 2307019145@qq.com
Products Intro: Cas:1538-09-6
ProductName:Penicillin G benzathine
Purity: 99% | Package: 25kg/RMB 88

Benzathine Penicillin manufacturers

  • Benzathine Penicillin
  • Benzathine Penicillin pictures
  • $10.00 / 1KG
  • 2021-08-31
  • CAS:1538-09-6
  • Min. Order: 1KG
  • Purity: 99.99%
  • Supply Ability: 20 tons/month
Benzathine Penicillin Basic information
Description
Product Name:Benzathine Penicillin
Synonyms:PENICILLIN-G BENZATHINE SALT;n,n'-dibenzylethylethylenediamine bis(benzylpenicillin);(2s,5r,6r)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid with n,n'-dibenzylethylenediamine (2:1);(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;benzathine benzylpenicillin;BENZYLPENICILLIN BENZATHINE SALT;N,N-dibenzylethylenediammonium bis(6-benzylpenicillanate);beacillin
CAS:1538-09-6
MF:C48H56N6O8S2
MW:909.12
EINECS:216-260-5
Product Categories:Organics;1538-09-6
Mol File:1538-09-6.mol
Benzathine Penicillin Structure
Benzathine Penicillin Chemical Properties
Melting point 123-124°
alpha D25 +206° (c = 0.105 in formamide)
solubility Very slightly soluble in water, freely soluble in dimethylformamide and in formamide, slightly soluble in ethanol (96 per cent).
color Crystals
CAS DataBase Reference1538-09-6
EPA Substance Registry System4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-, compd. with N,N'-bis(phenylmethyl)-1,2-ethanediamine (2:1) (1538-09-6)
Safety Information
Hazard Codes Xn
Risk Statements 22-42/43
Safety Statements 36
WGK Germany 3
RTECS XH9425000
ToxicityLD50 orl-mus: 2000 mg/kg NIIRDN 6,774,82
MSDS Information
Benzathine Penicillin Usage And Synthesis
DescriptionBenzathine penicillin and procaine penicillin is an antibiotic that fights bacteria in your body. Benzathine penicillin and procaine penicillin is used to treat many different types of severe infections, including strep and staph infections, diphtheria, meningitis, gonorrhea, and syphilis. It is also used to prevent rheumatic fever. It is given by injection into a muscle. Belonging to a penicillin-class drug, its mechanism of action is inhibiting the cell wall synthesis of bacteria, further killing bacteria.
Chemical PropertiesWhite or almost white powder.
OriginatorBicillin,Wyeth,US,1951
UsesThe benzathine salt of penicillin G, an antibiotic used in the treatment of various bacterial infections, including Staphylococcus aureus.
UsesBenzathine benzylpenicillin is used as a Penicillin antibacterial.
Manufacturing ProcessEthylenediamine (15 g, 0.25 mol) was added dropwise to 100 ml 98-100% formic acid in a two-necked 500 ml flask, fitted with an addition tube and reflux condenser with drying tube, cooled in an ice-bath. After complete addition of the base, 53 g of benzaldehyde (0.5 mol) was added in one lot. The ice-bath was removed and the flask was heated to the refluxing temperature. The initial rate of carbon dioxide evolution was too rapid to measure. After twenty minutes, the rate was circa 100 ml per minute and decreased rapidly to 8 ml per minute in one hour. Heating at reflux was continued for 35 hours.
Following the refluxing most of the excess formic acid was removed under reduced pressure. Hydrochloric acid (200 ml 6 N) was added to the viscous amber residue and heated under reflux, After 15 minutes, bumping necessitated cooling and filtering to remove crystalline dihydrochloride, which after washing with isopropanol was dried, MP circa 300°C. The mother liquors were refluxed one hour and cooled, obtaining an additional amount of product, MP circa 300°C. The filtrate was concentrated in vacuo to 100 ml, cooled and made alkaline with 40% NaOH. The supernatant oil was extracted with ether, dried, and fractionated from a stillpot packed with glass wool and heated in a sand-bath at 320°C. The first fraction at 106°C at 0.6-0.7 mm was Nbenzylethylenediamine (dipicrate, MP 222°C). The N,N'dibenzylethylenediamine was collected at 177°C to 206°C at 0.6-1.0 mm as a colorless liquid.
To a solution of 60 g of sodium penicillin G in 800 cc of distilled water cooled to 0°C to 4°C in an ice-bath, a solution of 35 g of N,N'dibenzylethylenediamine diacetate in 200 cc of distilled water is added dropwise with stirring. The thick slurry is filtered with suction, washed twice with 100 cc of cold water, dried by suction and spread out in a thin layer for completion of drying. The product weighed 80 g.
The air-dried powder has a broad melting point, sintering at 100°C, melting above 110°C to a cloudy liquid becoming clear at 135°C.
Therapeutic FunctionAntibacterial
Clinical UseSince penicillin G benzathine, N,N'-dibenzylethylenediaminedipenicillin G (Bicillin, Permapen), is the salt of a diamine,2 moles of penicillin are available from each molecule. It isvery insoluble in water, requiring about 3,000 mL to dissolve1 g. This property gives the compound great stabilityand prolonged duration of effect. At the pH of gastric juice,it is quite stable, and food intake does not interfere with itsabsorption. It is available in tablet form and in several parenteralpreparations. The activity of penicillin G benzathineis equivalent to 1,211 units/mg.Several other amines have been used to make penicillinsalts, and research is continuing on this subject. Otheramines that have been used include 2-chloroprocaine; L-Nmethyl-1,2-diphenyl-2-hydroxyethylamine (L-ephenamine);dibenzylamine; tripelennamine (Pyribenzamine); and N,N'-bis-(dehydroabietyl)ethylenediamine (hydrabamine).
Safety ProfileModerately toxic by ingestion andintraperitoneal routes. Experimental reproductive effects.When heated to decomposition it emits very toxic fumesof NOx and SOx. See other penicillin entries.
Benzathine Penicillin Preparation Products And Raw materials
Raw materialsPenicillin G sodium salt-->Benzaldehyde-->Ethylenediamine
Tag:Benzathine Penicillin(1538-09-6) Related Product Information
N,N-Dimethylformamide Sodium 1-heptanesulfonate Dimethyl ether Dacthal Dimethyl fumarate Dimethyl carbonate ETHANE Dimethyl sulfoxide Heptane N,N'-DIBENZYLETHYLENEDIAMINE Carbenicillin disodium Penicillin G potassium salt Penicillin G Cloxacillin benzathine Carbenicillin Disodium Salt Azlocillin Amoxicillin trihydrate CARBENICILLIN PHENYL SODIUM