Cephalothin sodium
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Category | Antibiotics |
Catalog number | BBF-04538 |
CAS | 58-71-9 |
Molecular Weight | 418.41 |
Molecular Formula | C16H15N2NaO6S2 |
Purity | ≥98% |
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Description
Cephalothin sodium is a semisynthetic first generation cephalosporin antibiotic having a broad spectrum of antibacterial activity that is administered parenterally used to prevent infection during surgery and to treat many kinds of infections of the blood, bone or join. It is active against gram-positive and gram-negative bacteria.
Specification
Related CAS | 153-61-7 (free acid) |
Synonyms | 7-(Thiophene-2-acetamido)cephalosporanic acid sodium; (6R,7R)-3-[(Acetyloxy)methyl]-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt; 7-[2-(2-Thienyl)acetylamido]cephalosporanic Acid Sodium Salt; CT Sodium; Sodium Cefalotin; Sodium Cephalotin; Keflin; Seffin; Toricelocin |
Shelf Life | As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly |
Storage | Store at -20°C under inert atmosphere |
IUPAC Name | sodium;(6R,7R)-3-(acetyloxymethyl)-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate |
Canonical SMILES | CC(=O)OCC1=C(N2C(C(C2=O)NC(=O)CC3=CC=CS3)SC1)C(=O)[O-].[Na+] |
InChI | InChI=1S/C16H16N2O6S2.Na/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10;/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23);/q;+1/p-1/t12-,15-;/m1./s1 |
InChI Key | VUFGUVLLDPOSBC-XRZFDKQNSA-M |
Source | Semi-synthetic |
Properties
Appearance | White to Off-white Solid |
Application | Anti-Bacterial Agents |
Antibiotic Activity Spectrum | Gram-positive bacteria; Gram-negative bacteria |
Boiling Point | 757.2°C at 760 mmHg |
Melting Point | >163°C |
Solubility | Slightly soluble in Chloroform, DMSO (Heated), Methanol (Heated), Water |
Reference Reading
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2