ChemicalBook >> CAS DataBase List >>Benzathine benzylpenicillin

Benzathine benzylpenicillin

CAS No.
1538-09-6
Chemical Name:
Benzathine benzylpenicillin
Synonyms
Penicillin G Benzathin;bicillin;permapen;BENZATHINE PENICILLIN;Benzathine Pencillin G;neolin;penadur;benzapen;cillenta;dibencil
CBNumber:
CB0400046
Molecular Formula:
C48H56N6O8S2
Molecular Weight:
909.12
MDL Number:
MFCD00079284
MOL File:
1538-09-6.mol
MSDS File:
SDS
Last updated:2024-04-24 17:21:45

Benzathine benzylpenicillin 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 Reference 1538-09-6
FDA UNII SSZ1S4I0US
ATC code J01CE08
EPA Substance Registry System 4-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

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H334
Precautionary statements  P261-P264-P270-P284-P301+P312-P304+P340+P312
Hazard Codes  Xn
Risk Statements  22-42/43
Safety Statements  36
WGK Germany  3
RTECS  XH9425000
Toxicity LD50 orl-mus: 2000 mg/kg NIIRDN 6,774,82

Benzathine benzylpenicillin price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich B0500000 Benzathine benzylpenicillin 1538-09-6 b0500000 $220 2024-03-01 Buy
Sigma-Aldrich 31735 Benzathine penicilline G tetrahydrate VETRANAL 1538-09-6 250mg $59.1 2022-05-15 Buy
TRC P223518 PenicillinGBenzathineSaltwith0.2%Polysorbate80 1538-09-6 250mg $75 2021-12-16 Buy
TRC P223518 PenicillinGBenzathineSaltwith0.2%Polysorbate80 1538-09-6 500mg $115 2021-12-16 Buy
Usbiological 287318 Penicillin G benzathine anhydrous 1538-09-6 500mg $326 2021-12-16 Buy
Product number Packaging Price Buy
B0500000 b0500000 $220 Buy
31735 250mg $59.1 Buy
P223518 250mg $75 Buy
P223518 500mg $115 Buy
287318 500mg $326 Buy

Benzathine benzylpenicillin Chemical Properties,Uses,Production

Description

Benzathine 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 Properties

White or almost white powder.

Originator

Bicillin,Wyeth,US,1951

Uses

The benzathine salt of penicillin G, an antibiotic used in the treatment of various bacterial infections, including Staphylococcus aureus.

Uses

Benzathine benzylpenicillin is used as a Penicillin antibacterial.

Manufacturing Process

Ethylenediamine (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 Function

Antibacterial

Clinical Use

Since 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 Profile

Moderately 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 benzylpenicillin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 164)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 1000 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+86-13474506593 +86-13474506593 sarah@tnjone.com China 874 58
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15928 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
HubeiwidelychemicaltechnologyCo.,Ltd
18627774460 faith@widelychemical.com CHINA 742 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3586 58

View Lastest Price from Benzathine benzylpenicillin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Benzylpenicillin Benzathine pictures 2024-04-24 Benzylpenicillin Benzathine
1538-09-6
US $0.00 / kg 1kg 99% 10000kg Shaanxi TNJONE Pharmaceutical Co., Ltd
Benzathine Benzylpenicillin pictures 2024-04-12 Benzathine Benzylpenicillin
1538-09-6
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Benzathine Benzylpenicillin pictures 2024-04-12 Benzathine Benzylpenicillin
1538-09-6
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
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 benzacillin benzapen benzathinepenicilling benzethacil benzylpenicillinbenzathine benzylpenicillindibenzylethylenediaminesalt bica-penicillin cepacilina cillenta debecillin debecylina diaminepenicillin diaminocillina dibencil dibencillin dibenzylethylenediamine-di-penicilling durabiotic dura-penita duropenin extencilline extenicilline henylacetamido)-,compd.withn,n’-dibenzylethylenediamine(2:1) lentocillin lentopenil leomypen longacilina longicil megacillinsuspension moldamin n,n’-dibenzyl-ethylenediamincompd.withpenicilling(1:2) n,n’-dibenzylethylenediamine,compoundedwithpenicilling(1:2) n,n’-dibenzylethylenediaminebis(benzylpenicillin) n,n’-dibenzylethylenediaminesaltofbenzylpenicillin nci-c56100 neolin nylacetyl)amino]-[2s-(2alpha,5alpha,6beta)]-,compd.withn,n’-bis(phenylme penadur penadurl-a pendepon pen-di-ben penditan penduran penicilling,benzathine penicilling,compd.withn,n’-dibenzylethylenediamine(2:1) penicillingbenzathine penicillin-gbenzathine penicillingsaltofn,n’-dibenzylethylenediamine penidural penidure tardocillin