Penicillin G potassium salt

Penicillin G potassium salt Basic information
Product Name:Penicillin G potassium salt
Synonyms:tabilin;PENICILLIN G K-SALT;PENICILLIN G POTASSIUM SALT;PENICILLIN G POTASSIUM;potassium [2s-(2alpha,5alpha,6beta)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate;potassium benzylpenicillin;4-Thia-1-azabicyclo;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-, [2S-(2alpha,5alpha,6beta)]-, monopotassium salt
CAS:113-98-4
MF:C16H17KN2O4S
MW:372.48
EINECS:204-038-0
Product Categories:Heterocycles;Intermediates & Fine Chemicals;Antibiotics for Research and Experimental Use;API's;Pharmaceuticals;Sulfur & Selenium Compounds;beta-Lactams (Antibiotics for Research and Experimental Use);Biochemistry;113-98-4
Mol File:113-98-4.mol
Penicillin G potassium salt Structure
Penicillin G potassium salt Chemical Properties
Melting point 214-217 C
alpha D22 +285° (c = 0.748 in water)
refractive index 294 ° (C=1, H2O)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility H2O: 100 mg/mL
form powder
color Needles from butanol (aq)
PHpH (10g/L, 25℃) : 5.0~7.5
Water Solubility Soluble in water (100 mg/ml), methanol, ethanol (sparingly), and alcohol. Insoluble in chloroform.
Merck 14,7094
BRN 3832841
Stability:Hygroscopic
InChIKeyIYNDLOXRXUOGIU-LQDWTQKMSA-M
EPA Substance Registry SystemPenicillin G Potassium (113-98-4)
Safety Information
Hazard Codes Xn,C,F
Risk Statements 42/43-34-11
Safety Statements 36/37-45-36/37/39-26-16-60-37-24-22
WGK Germany 2
RTECS XH9700000
10-23
TSCA Yes
HS Code 29411000
ToxicityLD50 oral in rabbit: 5848mg/kg
Penicillin G potassium salt Usage And Synthesis
Chemical PropertiesPenicillin G potassium salt is also known as Potassium benzylpenicillin, it is white crystalline powder, odorless or slightly specific odor, hygroscopic. Soluble in water, physiological saline, glucose solution. The aqueous solution of it is easy to fail when placed at room temperature, and it will fail rapidly in the presence of acid, alkali, oxidant, etc. Penicillin G potassium salt has good antibacterial effect on Streptococcus such as Streptococcus hemolyticus, Streptococcus pneumoniae and Staphylococcus without penicillinase.
UsesPenicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. Penicillin G potassium salt is used as a cell culture additive as an antibiotics. Use to inhibit the synthesis of bacterial cell walls by inhibition of the cell wall peptidoglycan chain cross-lining. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans.
PreparationPenicillin G potassium salt is a highly effective and low toxicity antibiotic, which is obtained by salt formation of Chlorpheniramine maleate and maleic acid.
DefinitionChEBI: Penicillin G potassium salt is organic potassium salt of benzylpenicillin. It is an antibiotic substance produced by Penicillium sp. Antibacterial. It contains a benzylpenicillin(1-).
Brand namePentids (Apothecon); Pfizerpen (Pfizer).
General DescriptionPenicillin G Potassium is the potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic. Penicillin G potassium binds to penicillin binding proteins (PBP), the enzymes that catalyze the synthesis of peptidoglycan, which is a critical component of the bacterial cell wall. This leads to the interruption of cell wall synthesis, consequently leading to bacterial cell growth inhibition and cell lysis.
Biochem/physiol ActionsMode of Action: Penicillin G acts by inhibiting cell wall synthesis through binding to penicillin binding proteins (PBPs), inhibiting peptidoglycan chain cross-linking.
Antimicrobial spectrum: This product is active against gram-positive and gram-negative bacteria.
Safety ProfilePoison by intracerebral andintravenous routes. Moderately toxic by intraperitonealroute. Mutation data reported. See other penicillin entries.When heated to decomposition it emits toxic fumes ofNOx and SOx.
AMOXYCILLIN SODIUM/POTASSIUM CLAVULANATE Heptane BENZYLPENICILLIN POTASSIUM, [ACETAMIDO-1,2-14C]- Penicillin G BENZYLPENICILLIN POTASSIUM, [BENZYL-14C] Potassium iodide Potassium sorbate AMOXICILLIN, CLAVULANATE POTASSIUM(4:1) Potassium bromate Potassium persulfate Carbenicillin Disodium Salt Potassium Citrate Potassium Acetate Potassium chloride Sodium 1-heptanesulfonate Potassium BENZYLPENICILLINATE-D7, POTASSIUM SALT Potassium nitrate Benzylpenicillin Potassium

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