Compound Profile

Cadaverine

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Cadaverine, a foul-smelling organic compound derived from decaying flesh, may seem disconnected from everyday life to many individuals. However, the relevance of cadaverine lies in its applications in diverse industries, including food preservation, pharmaceuticals, and even in the field of forensics. In the food industry, cadaverine is sometimes used as a flavor enhancer due to its unique taste profile. In pharmaceuticals, it is utilized in the synthesis of certain drugs. Additionally, cadaverine can play a crucial role in forensic investigations as its presence can indicate the decomposition of organic matter. Thus, while cadaverine may not be a topic of daily conversation, its practical implications are noteworthy in various aspects of modern life.

Table of Contents:

💡 Commercial Applications

Cadaverine, also known as 1,5-pentanediamine, has various commercial and industrial applications. In the leather and textile industry, it is used as a chemical intermediate for the synthesis of polyamides and polyurethanes. It is also used in the manufacture of insecticides, dyes, and pharmaceuticals.

In the food industry, cadaverine is used as a flavorant and as a precursor for the production of biodegradable plastic. It is also used in the preservation of fish and meat products due to its antimicrobial properties. Additionally, it is utilized in the production of odorants and fragrances.

In terms of drug and medication applications, cadaverine has been explored for its potential antimicrobial properties. Research has shown that it may have activity against various bacteria and fungi, making it a potential candidate for the development of new antibiotics. Additionally, it has been studied for its potential role in cancer therapy, as it may have anti-tumor effects.

⚗️ Chemical & Physical Properties

Cadaverine is a colorless, viscous liquid with a putrid, foul odor similar to that of decaying flesh. It is often described as having a strong, unpleasant smell that is detectable at very low concentrations.

With a molar mass of 102.17 g/mol and a density of approximately 0.84 g/cm3, cadaverine is heavier than common household items such as water (molar mass of 18.02 g/mol, density of 1 g/cm3) and ethanol (molar mass of 46.07 g/mol, density of 0.79 g/cm3).

Cadaverine has a melting point of around -92°C and a boiling point of approximately 167°C. These values are much higher than those of common household items such as water (melting point of 0°C, boiling point of 100°C) and ethanol (melting point of -114.1°C, boiling point of 78.37°C).

Cadaverine is sparingly soluble in water, with a solubility of approximately 0.63 g/L at 20°C. It also has a relatively high viscosity, making it thicker than water and many common household liquids. This contrasts with substances like salt (high solubility in water) and vegetable oil (lower viscosity).

🏭 Production & Procurement

Cadaverine, a foul-smelling diamine compound, is primarily produced through the decarboxylation of the amino acid lysine. This process involves the enzymatic breakdown of lysine by lysine decarboxylase, resulting in the formation of cadaverine.

The procurement and transportation of cadaverine typically involve its extraction from biological sources such as bacteria or mammalian tissue. Bacteria such as Escherichia coli are commonly used as production hosts for cadaverine due to their ability to efficiently produce the compound. Once extracted, cadaverine can be purified and transported in liquid or solid form for various applications.

In industrial settings, cadaverine can be procured through fermentation processes using genetically engineered microorganisms. These microorganisms are designed to efficiently produce cadaverine through metabolic pathways that convert glucose or other sugars into the desired compound. The resulting cadaverine can then be harvested and processed for commercial use.

⚠️ Safety Considerations

Safety considerations for Cadaverine include its potential irritant effects on the skin, eyes, and respiratory system. It is important to handle Cadaverine with proper personal protective equipment, such as gloves and goggles, to prevent direct contact. In case of accidental exposure, it is advised to immediately flush the affected area with copious amounts of water and seek medical attention if irritation persists. Additionally, Cadaverine should be stored in a cool, dry, and well-ventilated area away from incompatible substances to prevent any potential reactions or hazards.

The pharmacology of Cadaverine involves its role as a diamine compound that is naturally found in living organisms, including certain types of bacteria. It is known for its strong and unpleasant odor, often described as resembling the smell of decaying flesh. In laboratory settings, Cadaverine is often used as a reagent in biochemical research to study its effects on cell growth and metabolism. Its pharmacological properties include its ability to bind to certain receptors in the body and potentially affect cellular processes.

Hazard statements for Cadaverine include its classification as a skin and eye irritant, as well as a respiratory irritant. Exposure to Cadaverine may cause irritation or burning sensations on the skin, eyes, and respiratory tract. Prolonged or repeated exposure to Cadaverine may lead to more severe health effects, such as respiratory distress or dermatitis. It is important to handle Cadaverine with caution and follow proper safety protocols to minimize the risk of exposure and potential health hazards.

Precautionary statements for Cadaverine include wearing appropriate personal protective equipment, such as gloves, goggles, and a lab coat, when handling the substance. It is recommended to work with Cadaverine in a well-ventilated area to minimize exposure to fumes or vapors. In case of accidental exposure, it is advised to wash the affected area thoroughly with soap and water and seek medical attention if necessary. Additionally, proper storage and handling practices should be followed to prevent spills, leaks, or contamination of the surrounding environment.

🔬 Potential Research Directions

Research on Cadaverine, a polyamine produced by the decarboxylation of lysine, has potential applications in various fields. In the realm of medicine, exploring the role of Cadaverine in diseases such as cancer and neurodegenerative disorders could lead to new treatment strategies. Additionally, studies on its antimicrobial properties have implications for the development of novel antibiotics.

Further investigation into the biosynthesis pathways of Cadaverine in different organisms could shed light on its ecological functions. Understanding how Cadaverine contributes to the interactions between microbes and their host organisms may aid in the development of new approaches for controlling harmful pathogens while preserving beneficial microbial communities.

In the area of food science, research on Cadaverine is crucial for ensuring food safety. Monitoring its levels in food products can help prevent the formation of harmful biogenic amines, which can cause food poisoning. Exploring methods to reduce Cadaverine concentrations in food could contribute to the development of safer food preservation techniques.

One similar compound to Cadaverine is Putrescine, with the molecular formula C4H12N2. Putrescine is also a diamine like Cadaverine, but differs in having a shorter carbon chain. It is commonly found in decaying animal tissue and contributes to the foul odor associated with decomposition.

Another related compound is Spermidine, with the molecular formula C7H19N3. Spermidine is a polyamine that shares some structural similarities with Cadaverine, but contains additional amine groups. It plays a role in cell growth and proliferation, and has been studied for its potential health benefits.

A third compound similar to Cadaverine is Spermine, with the molecular formula C10H26N4. Spermine is a polyamine with a longer carbon chain than Cadaverine, containing multiple amine groups. It is involved in various biological processes, including DNA stability and cell signaling pathways.

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