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Home > Encyclopedia > Penicillin G potassium

Penicillin G potassium

pharmaceutical raw materials
Penicillin G potassium structure

Penicillin G potassium 

structure
  • CAS No:

    113-98-4

  • Formula:

    C16H18N2O4S.K

  • Chemical Name:

    Penicillin G potassium

  • Synonyms:

    4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]- (2S,5R,6R)-,potassium salt (1:1);4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-,monopotassium salt;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-[2S-(2α,5α,6β)]-,monopotassium salt;Penicillin G,potassium salt;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-,monopotassium salt;Benzylpenicillinic acid potassium salt;Benzylpenicillin potassium;Benzylpenicillin potassium salt;Eskacillin;Falapen;Hipercilina;Notaral;Penicillin G potassium;Pentids;Potassium benzylpenicillin;Potassium benzylpenicillinate;Potassium penicillin G;Tabilin;Potassium 2,2-dimethyl-6β-phenylacetamidopenam-3α-carboxylate;Forpen;Hylenta;Hyasorb;Cristapen;Monopen;Megacillin tablets;Scotcil;Potassium 6-(phenylacetamido)penicillanate;Novocillin vet.;Cosmopen;M-Cillin;Pentid;Crytapen;NSC 131815;Pfizerpen;55878-83-6

  • Categories:

    Active Pharmaceutical Ingredients  >  Antibiotics

Description

White powderChEBI: Organic potassium salt of benzylpenicillin.

Penicillin G potassium Basic Attributes

372.48

372.054596

204-038-0

29411000

Characteristics

115

-0.14510

powder

214-217 °C (decomp)

294 ° (C=1, H2O)

soluble in water (100 mg/ml), methanol, ethanol (sparingly), and alcohol. Insoluble in chloroform.

2-8°C

Oral-rat LD50; 6700 mg/kg; Oral-Mouse LD50: 6257 mg/kg

Flammable; burning produces toxic nitrogen oxides and sulfur oxide fumes

D22 +285° (c = 0.748 in water)

Safety Information

NONH for all modes of transport

2

42/43-34-11

36/37-45-36/37/39-26-16-60-37-24-22

XH9700000

Xn,C,F

Ventilated, low temperature and dry

P280

H317

Toxicity

practically nontoxic

Penicillin G potassium Use and Manufacturing

Methods of Manufacturing

A series of experiments was carried out in which to 1000 ml of an activated- carbon-treated extract containing approximately 100, 000 Oxford Units Penicillin G per ml in n-butylacetate, a 50percent (w/w) solution of KTo 1000 ml of an activated-carbon-treated extract containing approximately 100, 000 Oxford Units Penicillin G per ml (1 Oxford Unit equals circa 0.6 microgram of penicillin G) in n-butylacetate, a 30percent (w/w) solution of K

Uses

An antibiotic substance produced by Penicillium sp. Antibacterial.

4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]- (2S,5R,6R)-, potassium salt (1:1): ACTIVE

Computed Properties

Molecular Weight:372.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:372.05460969
Monoisotopic Mass:372.05460969
Topological Polar Surface Area:115
Heavy Atom Count:24
Complexity:536
Undefined Atom Stereocenter Count:3
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Penicillin has good antibacterial effect on hemolytic streptococci and other streptococci, Streptococcus pneumoniae and non-penicillinase-producing staphylococci. It has moderate antibacterial effect on enterococci. Neisseria gonorrhoeae, Neisseria meningitidis, Corynebacterium diphtheriae, Bacillus anthracis, Actinomyces bovis, Streptobacillus candida, Listeria monocytogenes, Leptospira and Treponema pallidum are sensitive to this product. This product also has certain antibacterial activity against Haemophilus influenzae and Bordetella pertussis, and other Gram-negative aerobic or facultative anaerobic bacteria are less sensitive to this product. This product has good antibacterial effect on Clostridium, Peptostreptococcus anaerobic bacteria and melanin-producing Bacteroides, but has poor antibacterial effect on Bacteroides fragilis. Penicillin exerts its bactericidal effect by inhibiting bacterial cell wall synthesis.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • ACS DOBFAR SPA

    Italy Italy
    Active
  • CSPC Zhongnuo PHARMACEUTICAL(Shijiazhuang) Co., Ltd.

    China China
    Active
  • Jiangxi Dongfeng Pharmaceutical Co., Ltd.

    China China
    Active

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