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Procaine penicillin G

CAS No.
54-35-3
Chemical Name:
Procaine penicillin G
Synonyms
PENICILLIN G PROCAINE;PROCAINE BENZYLPENICILLIN;benzylpenicillin procaine;duphapen;depocillin;hostacillin;hydracillin;rocaine penicillin;Procain-Penicillin;Procain Penicillin G
CBNumber:
CB0731029
Molecular Formula:
C29H38N4O6S
Molecular Weight:
570.7
MDL Number:
MFCD00079285
MOL File:
54-35-3.mol
MSDS File:
SDS
Last updated:2023-11-21 19:54:38

Procaine penicillin G Properties

Melting point 129-130 °C
Density 1.1335 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. Store at -20°C
solubility DMSO: 100 mg/mL (175.22 mM);Ethanol: 20 mg/mL (35.04 mM)
Water Solubility Water: 10 mg/mL (17.52 mM)
CAS DataBase Reference 54-35-3
FDA UNII 1LW5K9CIR1
ATC code J01CE09
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 2-(diethylamino)ethyl 4-aminobenzoate (1:1) (54-35-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Toxicity LD50 orl-rat: >2 g/kg ABANAE 3,534,55/56

Procaine penicillin G price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
AK Scientific O634 ProcainepenicillinG 54-35-3 100mg $89 2021-12-16 Buy
American Custom Chemicals Corporation API0027913 PROCAINE BENZYL PENICILLIN 95.00% 54-35-3 5MG $458.16 2021-12-16 Buy
Product number Packaging Price Buy
O634 100mg $89 Buy
API0027913 5MG $458.16 Buy

Procaine penicillin G Chemical Properties,Uses,Production

Chemical Properties

White, fine crystals or powder; odorless; relatively stable to air and light; solutions dextroro- tatory. Sparingly soluble in water; slightly soluble in alcohol; fairly soluble in chloroform.

Originator

Duracillin,Lilly,US,1948

Uses

Antibacterial.

Manufacturing Process

There was added to 250 ml of a concentrated butyl acetate extract containing 74,000 units of the acid form of penicillin per ml, 50 ml of a butyl acetate solution containing 0.238 g per ml of procaine base. The solution was agitated for one hour. The precipitate which formed was very gummy and not in the form of discrete crystals. This precipitate was crystallized by scratching the side of the vessel and agitating further. After this treatment 18.25 g of crystalline procaine penicillin was obtained which assayed 1010 units per mg representing a yield of 99.6% of the activity contained in the concentrated extract.

brand name

Duracillin(Lilly); Pfizerpen (Pfizer).

Therapeutic Function

Antibacterial

General Description

The first widely used amine salt of penicillin G wasmade with procaine. Penicillin G procaine (Crysticillin,Duracillin, Wycillin) can be made readily from penicillin Gsodium by treatment with procaine hydrochloride. This saltis considerably less soluble in water than the alkali metalsalts, requiring about 250 mL to dissolve 1 g. Free penicillinis released only as the compound dissolves and dissociates.It has an activity of 1,009 units/mg. A large number ofpreparations for injection of penicillin G procaine are commerciallyavailable. Most of these are either suspensions inwater to which a suitable dispersing or suspending agent, a buffer, and a preservative have been added or suspensions inpeanut oil or sesame oil that have been gelled by theaddition of 2% aluminum monostearate. Some commercialproducts are mixtures of penicillin G potassium or sodiumwith penicillin G procaine; the water-soluble salt providesrapid development of a high plasma concentration of penicillin,and the insoluble salt prolongs the duration of effect.

Safety Profile

Moderately toxic by intraperitoneal and intramuscular routes. Slightly toxic by ingestion and subcutaneous routes. When heated to decomposition it emits toxic vapors of NOx, and SOx.

113-98-4
59-46-1
54-35-3
Synthesis of Procaine penicillin G from Penicillin G potassium salt and Procaine

Procaine penicillin G Preparation Products And Raw materials

Global( 157)Suppliers
Supplier Tel Email Country ProdList Advantage
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View Lastest Price from Procaine penicillin G manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Procaine Penicillin G pictures 2024-04-24 Procaine Penicillin G
54-35-3
US $0.00 / kg 1kg 99% 10000kg Shaanxi TNJONE Pharmaceutical Co., Ltd
Procaine penicillin G pictures 2024-04-12 Procaine penicillin G
54-35-3
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Procaine penicillin G pictures 2023-11-21 Procaine penicillin G
54-35-3
US $0.00-0.00 / kg 1kg 99% 50000kg Hebei Yibangte Import and Export Co. , Ltd.
BENZYLPENICILLIN PROCAINE + POTASSIC 3:1 Penicillin G procaine Benzylpenicillin procaine API Sterile Penicillin G Procaine/SodiuM3∶1 API BENZYLPENICILLIN PROCAIN SALT PROCAINE PENICILLIN G PENICILLIN-G PROCAIN SALT Procaine penicillin G(1% lecithin/citrate acid) Penicillin G procaine +1% lecithin CP200/BP/USP/EP Procain Penicillin G Penicillin G procaine sterile CP200/BP/USP/EP PROCAINE BENZYLPENICILLIN (PROCAINE PENICILLIN) ASSAY STANDARD BP(CRM STANDARD) PROCAINE BENZYLPENICILLIN EPP(CRM STANDARD) Benzylpenicillinic acid, procaine Procaine benzylpenicillinate benzylpenicillin novocaine salt depocillin duphapen hostacillin hydracillin 4-Thia-1-azabicyclo3.2.0heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(phenylacetyl)amino- (2S,5R,6R)-, compd. with 2-(diethylamino)ethyl 4-aminobenzoate (1:1) rocaine penicillin Procaine penicillin G USP/EP/BP Procaine penicillin G(fortified) USP/EP/BP PENICILLIN G PROCAINE USP/EP/BP Penicillin G Procaine/Sodium 3:1 USP/EP/BP Procain-Penicillin Benzyl Pencillin Procaine Penicillin G. ProcaineQ: What is Penicillin G. Procaine Q: What is the CAS Number of Penicillin G. Procaine Q: What is the storage condition of Penicillin G. Procaine (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(1-oxo-2-phenylethyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid PROCAINE BENZYLPENICILLIN PENICILLIN G PROCAINE benzylpenicillin procaine 54-35-3 54-35-2 C16H18N2O4SC13H20N2O C29H38N4O6S C16H18N2O4SC13H20N2O2 PHARMACEUTICALS 54-35-3