Alkanes, the simplest and most fundamental class of hydrocarbons, are characterized by their single covalent bonds between carbon atoms. This section delves into the methods of preparation, key chemical reactions, and the diverse applications of alkanes. General Methods of Preparation Catalytic Hydrogenation: Alkenes and alkynes are converted to alkanes by the addition of hydrogen in … Read more
Alkanes Definition and Classification Alkanes, also known as paraffins, are the simplest class of hydrocarbons, consisting only of carbon (C) and hydrogen (H) atoms with single covalent bonds. The general formula for alkanes is CnH2n+2. Types of Alkanes Straight-chain (Normal) Alkanes: Carbon atoms connected in a linear sequence without branches. Denoted as “n-” (e.g., n-pentane). … Read more
Limit tests is an analytical method used to determine whether the concentration of a specific impurity or substance in a pharmaceutical product is below a predefined acceptable limit. It ensures the quality, safety, and efficacy of the drug by controlling potentially harmful impurities. Types of Limit Tests: Qualitative Limit Tests: Provide a pass/fail result, indicating … Read more
Factors Affecting Microbial Spoilage is influenced by a combination of intrinsic and extrinsic factors. Intrinsic Factors Affecting Microbial Spoilage Water Activity (aw) Definition: The availability of water for microbial growth. Impact: Higher aw values support microbial proliferation. Control: Reducing aw through drying or adding humectants. pH Definition: Acidity or alkalinity of the product. Impact: Most … Read more
Sources of microbial contaminants include sewage, animal waste, agricultural runoff, and contaminated water supplies. 1. Raw Materials as a Sources of microbial contaminants: Water: Used in formulations can be a significant source of microbial contamination if not properly treated. Active Pharmaceutical Ingredients (APIs): May harbour contaminants from their source or during processing. Excipients: Ingredients like … Read more
Types of Spoilage in Pharmaceutical Products is spoilage in pharmaceuticals can be categorized into three main types: While all types are important, microbial spoilage is the focus here due to its direct impact on product safety. 1.Chemical Spoilage in Pharmaceutical Products Definition: Degradation of the active pharmaceutical ingredient (API) or excipients due to chemical reactions. … Read more
Assessment of a New Antibiotic is assessing a new antibiotic involves several key steps to ensure its efficacy, safety, and suitability for clinical use. Here’s a concise overview of the process: 1.In Vitro Testing of Assessment of a New Antibiotic Microbiological Assays: Minimum Inhibitory Concentration (MIC): Determine the lowest concentration that inhibits visible growth of … Read more
Methods for Standardization of Amino Acids is the Standardizing amino acids using microbiological assays involves measuring the response of specific microorganisms that require particular amino acids for growth. Here’s an overview of the methods typically used for this purpose: 1. Titrimetric Methods for Standardization of Amino Acids Principle: Based on the diffusion of amino acids … Read more
IUPAC Systems (International Union of Pure and Applied Chemistry) has established a standardized system for naming organic compounds, ensuring clear and unambiguous communication among chemists. IUPAC system applies to open-chain (aliphatic) compounds, carbocyclic compounds, and compounds containing functional groups. Below is a concise overview of the IUPAC systems nomenclature system for organic compounds with up to … Read more
Methods for Standardization of Vitamins Using Microbiological Assays standardizing vitamins using microbiological assays ensures the accuracy and reliability of their concentration in various products. Two primary methods used for this purpose are the turbidimetric assay and the titrimetric method. Here’s a brief overview of each: 1. Titrimetric Method Principle: Measures the amount of vitamin needed … Read more
