Soaps, Detergents, and Pharmaceuticals Lecture Flashcards

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Vocabulary style flashcards covering soaps, saponification, industrial detergent chemistry, quality control tests, classification of pharmaceuticals, and tablet manufacturing methods from lecture notes.

Last updated 2:58 AM on 10/5/26
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39 Terms

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Soaps

Sodium or potassium salts of long chain fatty acids such as oleic, steric, lauric, and palmitic acid, present in fats and oils in the form of glycerides.

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Hard soaps

Sodium salts of long chain fatty acids sourced mainly from tallow, animal fats, and coconut oils that are moderately soluble in water and do not lather easily.

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Soft soaps

Potassium salts of long chain fatty acids derived from linseed oil, castor oil, and vegetable oils that dissolve quickly, lather readily, and perform better in cleansing.

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Saponification

The process of making soap by the alkaline hydrolysis of vegetable or animal fats/oils to yield glycerol and fatty acid salts.

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Industrial soaps

Key components of lubricating greases and thickeners made from metallic soaps like calcium, magnesium, aluminum, zinc, copper, or lead.

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Resin

A plant product containing abietic acid added to soap formulations to accelerate lather formation, enhance cleansing action, and soften hard soaps.

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Salting out

The process during full boiled soap making where sodium chloride (NaCl\text{NaCl}) is added to separate the soap mixture, causing soap to rise to the top and glycerin to settle at the bottom.

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Superfatting agents

Soap additives such as lanolin added to replenish skin lipids removed by soap action, preventing skin from becoming rough and dry.

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Cold Process (Soap Manufacturing)

An elementary room-temperature batch soap making process where glycerine is retained in the soap and full saponification/curing takes several weeks.

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Semi-boiled Process

A soap production process using heated coils at 70–90 ∘C70\text{--}90\,^\circ\text{C} to accelerate saponification, releasing no effluent and allowing better additive integration.

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Full boiled process (Kettle process)

A soap manufacturing method conducted at temperatures up to 100 ∘C100\,^\circ\text{C} where glycerin is separated from soap using sodium chloride salting out.

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Detergents

Sodium salts of long chain alkyl hydrogen sulphate or long chain alkylbenzene sulphonic acids composed of surfactants and subsidiary ingredients like builders and fillers.

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Micelles

Aggregates formed by soap or detergent molecules in aqueous solutions that reach colloidal particle dimensions, facilitating the emulsification of oily dirt.

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Builder

A detergent additive (such as phosphates or zeolites) that enhances surfactant performance by sequestering or exchanging hardness ions (Ca2+\text{Ca}^{2+}, Mg2+\text{Mg}^{2+}), providing alkalinity, and suspending soil.

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Anionic surfactants

Surfactants whose cleansing properties reside in a long chain anion in solution, such as sulfated fatty alcohols.

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Non-Ionic Surfactants

Polyethylene oxide derivatives that lack ionic charges, solvate in water through hydrogen bonding, and serve as non-ionizing grease emulsifiers.

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Amphoteric (Zwitter) surfactants

Surfactants containing both cationic (basic nitrogen) and anionic (carboxyl or sulphonyl) groups, such as alkyloamide, used for mild cosmetics and shampoos.

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Cationic surfactants

Specialty surfactants featuring a cationic nitrogen head and a long hydrophobic chain, noted for antistatic, germicidal, and fabric softening qualities.

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Acid value test

A quality control test determining free acid content in fat, measured by the amount of KOH\text{KOH} needed for neutralization.

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Iodine value test

A quality control metric for unsaturation, calculated as the grams of iodine absorbed by 100 g100\,g of oil.

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Narcotic analgesics

Pain-relieving drugs such as morphine used for severe pain that interact with opiate receptors, possess physical dependence liability, and risk respiratory depression.

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Non-narcotic analgesics

Non-addictive, non-prescription antipyretic pain relievers such as aspirin and paracetamol used for mild pain and arthritis symptoms.

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Antiseptics

Germ-killing chemical agents formulated for application directly to living body tissue, such as Dettol (chloroxylenol and terpineol).

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Disinfectants

Germicidal chemicals meant for application strictly to non-living surfaces, such as chlorine and phenol solutions.

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Anti-fertility drugs

Contraceptive chemical agents composed of synthetic progesterone or progesterone-estrogen combinations (e.g., Norethisterone) that suppress pregnancy by inhibiting ovulation.

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Antidepressants

Psychotherapeutic agents used to treat mood disorders, originating with imipramine in 1959 and progressing to newer agents like fluoxetine.

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Antihistamines

Drugs used for symptomatic relief of allergic conditions by blocking immune system histamine action, including sedating types (bromopheniramine) and non-sedating types (astemizole, terfanadine).

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ACE Inhibitors

Angiotensin converting enzyme inhibitors (e.g., capropril, enalapril) that prevent conversion of Angiotensin 1 to Angiotensin 2 to prevent vasoconstriction and lower blood pressure.

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Calcium Channel Blockers

Antihypertensive agents (e.g., diltiazem, nifedipine) that slow calcium influx into arterial walls, reducing heart workload and dilating blood vessels.

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Antineoplastics

Cancer chemotherapy agents categorized into alkylating agents (cyclophosphamide), antimetabolites (fluoroacil), and platinum coordination complexes (cis-platin).

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Antiulcers

Inhibitors of gastric acid secretion used to treat peptic ulcers, classified into antacids, anticholinergics, and H2 receptor antagonists.

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Antipsychotics

Drugs used to manage serious psychiatric illnesses (e.g., clozapine), associated with potential neurological side effects like restlessness and Parkinsonism.

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Antiviral agents

Highly selective anti-infective medications targeting viral replication dependent on host cellular machinery, such as Zidovudine (HIV/AIDS) and Acyclovir (herpes).

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Diuretics

Agents (e.g., spironolactone, Amidoride, furosemide) that increase renal urine output to manage edema in congestive heart failure and reduce blood pressure.

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Transdermal Drug Delivery System (TDDS)

A patch-based dosage design that delivers active drugs through skin layers into systemic circulation at a controlled rate, bypassing gastrointestinal degradation and hepatic first-pass metabolism.

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Osmotic Drug Delivery System

An advanced drug release mechanism encased in a semi-permeable membrane that utilises osmotic pressure gradients to pump active drug out through laser-drilled orifices at a constant rate.

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Wet Granulation

A tablet manufacturing method where active drug and excipients are agglomerated using a liquid binder, wet-screened, dried, dry-sized, and compressed.

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Dry Granulation

A tablet preparation method where dry powder mixtures are compacted into large pieces or slugs via roller compaction or slugging and milled into granules without liquid binders or drying heat.

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Direct Compression

The simplest tableting method involving direct compaction of blended powder excipients and API without modifying particle size via granulation.