Procaine penicilline G hydrate

Procaine penicilline G hydrate Basic information
Product Name:Procaine penicilline G hydrate
Synonyms:abbocillin-dc;crysticillin;despacilina;distaquaine;duracillin;enylacetamido)-,compd.with2-(diethylamino)ethylp-aminobenzoate(1:1),mono;flo-cillin;flo-cillinaqueous
CAS:6130-64-9
MF:C29H38N4O6S
MW:570.71
EINECS:612-112-2
Product Categories:Agro-Products;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds
Mol File:6130-64-9.mol
Procaine penicilline G hydrate Structure
Procaine penicilline G hydrate Chemical Properties
Melting point 106-110° (with decompn)
density 1.255-1.256
storage temp. Refrigerator
solubility Slightly soluble in water, sparingly soluble in ethanol (96 per cent).
form neat
color White to Off-White
CAS DataBase Reference6130-64-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 42/43
Safety Statements 36
RTECS XH9450000
HS Code 2941102000
ToxicityLD50 s.c. in mice: 2.3 g/kg (Soehring)
MSDS Information
ProviderLanguage
Procaine penicilline G hydrate English
Procaine penicilline G hydrate Usage And Synthesis
Chemical PropertiesWhite Solid
UsesProcaine penicilline G hydrate is a composed of the β-lactam antibiotic of Penicillin G and the sodium channel blocker Procaine. As an antibiotic, Penicillin G is noted to posses effectiveness mainly against gram-positive organisms. Procaine Penicillin G is used a growth stimulant for poultry.
UsesProcaine Penicillin G is a composed of the β-lactam antibiotic of Penicillin G and the sodium channel blocker Procaine. As an antibiotic, Penicillin G is noted to posses effectiveness mainly against gram-positive organisms. Procaine Penicillin G is used a growth stimulant for poultry.
Brand nameDuracillin(Lilly); Pfizerpen (Pfizer).
Antimicrobial activityThe procaine salt of benzylpenicillin. Poorly soluble (1:200 in water). Administered intramuscularly as a suspension of crystals which slowly dissolve at the site of the injection.
It must not be given intravenously. Intramuscular administration produces a flat sustained plasma concentration of penicillin, which is much lower than that achieved by an equivalent dose of benzylpenicillin, with plasma levels still detectable 24 h later. An injection of 0.6 g yields a peak plasma concentration of 1–2 mg benzylpenicillin/L after 2–4 h. Free procaine is detectable in the plasma within 30 min.
Very severe and potentially fatal reactions resembling those of anaphylactic shock, but non-allergic in character, may occur, probably due to accidental entry into the vascular system at the site of injection and blockage of pulmonary and cerebral capillaries by crystals of the suspension. Reactions due to liberated procaine may include acute anxiety, hypertension, tachycardia, vomiting, audiovisual hallucinations and acute psychotic disturbance. The most severe reactions lead to convulsions and cardiac arrest. Other reactions are those to liberated benzylpenicillin.

Procaine penicilline G hydrate Preparation Products And Raw materials
Chloral hydrate Benzathine benzylpenicillin Procaine penicillin G hydrazine hydrate N,N-Dimethylformamide p-Toluenesulfonic acid monohydrate Citric acid monohydrate ETHANE Procaine penicilline G hydrate Dimethyl sulfide Dimethyl fumarate Dimethyl sebacate Dimethyl sulfoxide Dimethyl ether Dimethyl carbonate Penicillin G sodium salt hydrate PROCAINE Procaine Penicillin

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